POLH | Belgian Genetic Tests database

Analyte Export to PDF
Name:	DNA polymerase eta
Symbol:	POLH
Version of Orphanet:	2023-06-22 14:14:43
Synonyms:	RAD30A XP-V
XREF(s):	Orphanet Ensembl Genatlas HGNC OMIM Reactome SwissProt
Created:	13 May 2019 - 01:01
Changed:	22 Jun 2023 - 16:14

Related Genetic Tests

Related Diseases

Related Gene Panels

Ataxia (348 genes) - ULB

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Comments
AAAS	100.00	No comment
ABCB7	99.99	No comment
ABCD1	97.56	No comment
ABHD12	88.30	No comment
ABHD5	99.85	No comment
ACADVL	98.04	No comment
ACO2	100.00	No comment
COQ8A	99.92	No comment
AFG3L2	94.80	No comment
AHI1	100.00	No comment
ALAS2	100.00	No comment
ALDH18A1	100.00	No comment
ALDH5A1	84.13	No comment
ALG6	100.00	No comment
ALS2	100.00	No comment
AMACR	96.78	No comment
AMPD2	99.90	No comment
AMT	100.00	No comment
ANO10	100.00	No comment
AP1S2	100.00	No comment
APTX	99.96	No comment
ARL13B	99.98	No comment
ARL6	100.00	No comment
ARSA	100.00	No comment
ARX	100.00	No comment
ASPA	100.00	No comment
ATCAY	100.00	No comment
ATG5	100.00	No comment
ATL1	99.89	No comment
ATM	100.00	No comment
ATP1A3	100.00	No comment
ATP2B2	100.00	No comment
ATP2B3	99.89	No comment
ATP7B	100.00	No comment
ATP8A2	99.91	No comment
ATXN1	100.00	No comment
ATXN10	98.19	No comment
ATXN2	93.25	No comment
ATXN3	99.47	No comment
ATXN7	98.67	No comment
B9D1	99.89	No comment
BBS1	100.00	No comment
BBS10	100.00	No comment
BBS12	100.00	No comment
BBS2	100.00	No comment
BBS4	99.97	No comment
BBS5	100.00	No comment
BBS7	99.99	No comment
BBS9	99.93	No comment
BEAN1	100.00	No comment
BIVM	100.00	No comment
BSCL2	100.00	No comment
BTD	100.00	No comment
TWNK	100.00	No comment
MTRFR	100.00	No comment
C19ORF12	100.00	No comment
CPLANE1	100.00	No comment
CA8	100.00	No comment
CACNA1A	99.53	No comment
CACNA1G	99.97	No comment
CACNB4	99.95	No comment
CAMTA1	99.98	No comment
CAPN1	99.97	No comment
CASK	99.99	No comment
CC2D2A	100.00	No comment
CCDC88C	99.64	No comment
CEP290	100.00	No comment
CEP41	100.00	No comment
CHMP1A	100.00	No comment
CLCN2	100.00	No comment
CLN5	98.80	No comment
CLN6	90.40	No comment
CLPP	97.95	No comment
COA7	100.00	No comment
COASY	100.00	No comment
COG5	99.95	No comment
COQ2	99.66	No comment
COQ6	100.00	No comment
COQ9	100.00	No comment
COX20	95.39	No comment
CP	100.00	No comment
CRAT	99.29	No comment
CSTB	98.75	No comment
CWF19L1	100.00	No comment
CYP27A1	99.38	No comment
CYP2U1	93.20	No comment
CYP7B1	95.41	No comment
DARS1	100.00	No comment
DARS2	100.00	No comment
DDB2	100.00	No comment
DDHD2	100.00	No comment
DLAT	100.00	No comment
DMXL2	100.00	No comment
DNAJC19	99.65	No comment
DNAJC3	99.99	No comment
DNAJC5	100.00	No comment
DNMT1	99.54	No comment
EBF3	99.94	No comment
EEF2	100.00	No comment
EIF2B1	100.00	No comment
EIF2B2	99.61	No comment
EIF2B3	98.87	No comment
EIF2B4	100.00	No comment
EIF2B5	100.00	No comment
ELOVL4	100.00	No comment
ELOVL5	100.00	No comment
EPM2A	97.21	No comment
ERCC2	99.22	No comment
ERCC3	100.00	No comment
ERCC4	99.99	No comment
ERCC5	100.00	No comment
ETFA	100.00	No comment
ETFB	100.00	No comment
ETFDH	100.00	No comment
EXOSC3	100.00	No comment
FA2H	95.71	No comment
FARS2	100.00	No comment
FBXL4	100.00	No comment
FDXR	100.00	No comment
FGF14	100.00	No comment
FLVCR1	100.00	No comment
FMR1	99.99	No comment
FOLR1	100.00	No comment
FRMD7	99.98	No comment
FXN	100.00	No comment
GALC	98.98	No comment
GBA1	100.00	No comment
GBA2	100.00	No comment
GBE1	100.00	No comment
GCDH	100.00	No comment
GCLC	99.98	No comment
GCSH	73.97	No comment
GFAP	100.00	No comment
GJC2	96.72	No comment
GLB1	100.00	No comment
GLDC	97.39	No comment
GLRX5	100.00	No comment
GM2A	100.00	No comment
GOSR2	100.00	No comment
GPAA1	95.08	No comment
GPR143	89.09	No comment
ADGRG1	99.99	No comment
GRID2	100.00	No comment
GRM1	99.99	No comment
GSS	100.00	No comment
HARS2	100.00	No comment
HEPACAM	99.85	No comment
HERC1	100.00	No comment
HEXA	100.00	No comment
HEXB	99.19	No comment
HIBCH	100.00	No comment
HPRT1	92.71	No comment
HTRA1	75.65	No comment
IFRD1	98.86	No comment
IGDCC3	95.07	No comment
INPP5E	99.14	No comment
IRF2BPL	97.56	No comment
ITM2B	100.00	No comment
ITPR1	99.99	No comment
KCNA1	100.00	No comment
KCNC3	76.20	No comment
KCND3	100.00	No comment
KCNJ10	100.00	No comment
KCNJ6	100.00	No comment
KCNMA1	99.93	No comment
WASHC5	100.00	No comment
RUBCN	96.60	No comment
NEXMIF	100.00	No comment
KIF1A	98.74	No comment
KIF1C	100.00	No comment
KIF5A	100.00	No comment
KIF5C	100.00	No comment
KIF7	99.64	No comment
L2HGDH	99.75	No comment
LAMA1	99.79	No comment
LAMB1	100.00	No comment
LARS2	100.00	No comment
LMNB1	97.00	No comment
LRPPRC	98.80	No comment
LYST	100.00	No comment
MFSD8	100.00	No comment
MKKS	100.00	No comment
MKS1	100.00	No comment
MLC1	98.57	No comment
MMACHC	100.00	No comment
MME	100.00	No comment
MRE11	99.05	No comment
MSTO1	99.96	No comment
MTFMT	97.83	No comment
MTPAP	99.98	No comment
MTRR	100.00	No comment
MTTP	100.00	No comment
MVK	100.00	No comment
NANS	100.00	No comment
NDUFAF6	95.61	No comment
NDUFS1	100.00	No comment
NDUFS2	100.00	No comment
NDUFS4	99.96	No comment
NDUFS7	93.34	No comment
NDUFS8	100.00	No comment
NDUFV1	99.62	No comment
NEFL	99.62	No comment
NEU1	100.00	No comment
NHLRC1	96.01	No comment
NKX6-2	94.10	No comment
NOL3	100.00	No comment
NOP56	99.99	No comment
NOTCH3	93.46	No comment
NPC1	97.50	No comment
NPC2	100.00	No comment
NPHP1	100.00	No comment
NUBPL	99.92	No comment
OCLN	100.00	No comment
OFD1	97.13	No comment
MED12	99.98	No comment
OPA3	100.00	No comment
OPHN1	99.94	No comment
OTUD4	100.00	No comment
PAX6	100.00	No comment
PDGFRB	99.98	No comment
PDHX	100.00	No comment
PDSS1	85.11	No comment
PDSS2	100.00	No comment
PDYN	100.00	No comment
PEX10	87.10	No comment
PEX16	99.97	No comment
PEX2	100.00	No comment
PEX7	95.60	No comment
PHYH	99.81	No comment
PIK3R5	100.00	No comment
PLA2G6	100.00	No comment
PLEKHG4	100.00	No comment
PLP1	100.00	No comment
PMM2	100.00	No comment
PMPCA	100.00	No comment
PNKD	99.93	No comment
PNKP	99.84	No comment
PNPLA6	99.95	No comment
POLG	100.00	No comment
POLH	100.00	No comment
POLR3A	100.00	No comment
POLR3B	100.00	No comment
PPP2R2B	100.00	No comment
PRICKLE1	100.00	No comment
PRKCG	100.00	No comment
PRNP	99.92	No comment
PRPS1	99.91	No comment
PRRT2	100.00	No comment
PTEN	99.45	No comment
PUM1	100.00	No comment
RAB18	99.99	No comment
RAB3A	100.00	No comment
RAB3GAP1	100.00	No comment
RARS2	100.00	No comment
RELN	100.00	No comment
RNASEH2A	100.00	No comment
RNASEH2C	100.00	No comment
RNF170	100.00	No comment
RNF216	100.00	No comment
RPGRIP1L	96.40	No comment
RRM2B	100.00	No comment
SACS	99.95	No comment
SAMD9L	100.00	No comment
SAMHD1	100.00	No comment
SAR1B	100.00	No comment
SCN8A	100.00	No comment
SEC16A	99.98	No comment
SEPSECS	99.57	No comment
SERAC1	100.00	No comment
SETX	100.00	No comment
SIL1	99.95	No comment
SKOR1	98.57	No comment
SLC16A2	99.97	No comment
SLC17A5	100.00	No comment
SLC19A3	99.90	No comment
SLC1A3	100.00	No comment
SLC20A2	100.00	No comment
SLC25A15	100.00	No comment
SLC25A46	100.00	No comment
SLC2A1	100.00	No comment
SLC39A8	98.92	No comment
SLC52A2	100.00	No comment
SLC52A3	99.86	No comment
SLC9A1	100.00	No comment
SLC9A6	99.66	No comment
SMPD1	100.00	No comment
SNX14	99.98	No comment
SPAST	99.83	No comment
SPG11	100.00	No comment
SPG7	95.78	No comment
SPR	99.98	No comment
SPTBN2	99.93	No comment
SRD5A3	98.61	No comment
STUB1	99.69	No comment
SYNE1	100.00	No comment
SYT14	92.28	No comment
TANGO2	99.94	No comment
TBC1D20	95.06	No comment
TBCC	100.00	No comment
TBP	100.00	No comment
TCTN1	100.00	No comment
TCTN2	100.00	No comment
TCTN3	100.00	No comment
TDP1	100.00	No comment
TDP2	100.00	No comment
TGM6	100.00	No comment
TK2	100.00	No comment
TMEM138	100.00	No comment
TMEM216	99.87	No comment
TMEM231	100.00	No comment
TMEM237	99.85	No comment
TMEM240	96.75	No comment
TMEM67	99.95	No comment
ACD	99.99	No comment
TRIM32	100.00	No comment
TRPC3	99.48	No comment
TSEN2	100.00	No comment
TSEN34	100.00	No comment
TSEN54	91.60	No comment
TSFM	100.00	No comment
TTBK2	100.00	No comment
TTC19	100.00	No comment
TTC8	99.73	No comment
TTPA	96.80	No comment
TUBB4A	100.00	No comment
TUBG1	100.00	No comment
TYMP	100.00	No comment
UBA5	100.00	No comment
VAMP1	100.00	No comment
VLDLR	96.00	No comment
VPS13A	100.00	No comment
VPS13B	100.00	No comment
VPS13D	100.00	No comment
VRK1	100.00	No comment
VWA3B	100.00	No comment
WDPCP	99.11	No comment
WDR73	100.00	No comment
WDR81	99.63	No comment
WFS1	100.00	No comment
WWOX	100.00	No comment
XPA	98.10	No comment
XPC	100.00	No comment
XPR1	99.91	No comment
XRCC1	99.95	No comment
ZC4H2	100.00	No comment
ZFYVE26	100.00	No comment
ZNF423	100.00	No comment
ZNF592	100.00	No comment

Dermatogenetic / severe, rare and hereditary genodermatoses (394 genes) - ULB

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Comments
A2ML1	100.00
AAGAB	97.88
ABCA12	100.00
ABCB6	100.00
ABCC6	99.97
ABHD5	100.00
ACD	100.00
ADAM10	100.00
ADAMTS2	95.82
ADAR	100.00
AIM1	100.00
AKT1	100.00
ALDH18A1	100.00
ALDH3A2	99.94
ALOX12B	100.00
ALOXE3	100.00
ANTXR1	100.00
AP1S1	100.00
AP3B1	100.00
APCDD1	99.97
AQP5	99.87
ARHGAP31	100.00
ARSL	99.95
ASAH1	100.00
ATM	100.00
ATP2A2	100.00
ATP2C1	100.00
ATP6V0A2	99.98
ATP6V1A	100.00
ATP6V1E1	99.99
ATP7A	100.00
AXIN2	100.00
B3GALT6	63.11
B4GALT7	90.91
BANF1	97.55
BCS1L	100.00
BLM	100.00
BLOC1S3	95.69
BLOC1S6	100.00
BRAF	96.86
LRMDA	100.00
KDF1	100.00
CARD14	99.96
CBL	100.00
CBS	99.92
CD151	99.99
CDH3	100.00
CDK4	100.00
CDKN1B	100.00
CDKN2A	99.69
CDSN	99.93
CERS3	100.00
CHST14	99.81
CHST8	100.00
CHUK	99.59
CLCF1	100.00
CLDN1	100.00
CLDN10	100.00
COG6	100.00
COL11A1	100.00
COL12A1	100.00
COL17A1	100.00
COL1A1	100.00
COL1A2	99.41
COL3A1	99.99
COL5A1	98.23
COL5A2	100.00
COL7A1	100.00
CREBBP	99.98
CRLF1	89.67
CSTA	100.00
CTC1	99.71
CTSC	100.00
CYLD	100.00
CYP26C1	97.30
CYP4F22	99.27
DDB2	100.00
DIP2B	99.71
DKC1	99.92
DLL4	100.00
DLX3	99.95
DNMT1	99.69
DOCK6	99.13
DOLK	100.00
DSC3	98.96
DSE	100.00
DSG1	100.00
DSG2	99.89
DSG4	100.00
DSP	100.00
DST	100.00
DTNBP1	99.96
GLB1	100.00
ECM1	100.00
EDA	99.05
EDAR	100.00
EDARADD	100.00
EDN3	99.95
EDNRB	100.00
EFEMP2	100.00
ELN	99.96
ELOVL4	100.00
ENPP1	97.25
EOGT	100.00
EP300	100.00
EPG5	99.99
ERCC2	99.35
ERCC3	100.00
ERCC4	99.99
ERCC5	100.00
ERCC6	100.00
ERCC8	100.00
EVC	94.53
EVC2	98.69
EXPH5	100.00
F12	99.81
FAM111B	100.00
RETREG1	93.87
FAM83G	100.00
FBLN5	100.00
FBN1	100.00
FBN2	100.00
FERMT1	99.96
FGFR2	100.00
FGFR3	99.36
FH	100.00
FKBP14	100.00
FLCN	100.00
FGFR1	100.00
FLG2	100.00
FOXN1	100.00
FZD6	100.00
GALNT3	100.00
GAN	98.95
GBA1	100.00
GGCX	99.91
GHR	99.21
GJA1	100.00
GJB2	100.00
GJB3	100.00
GJB4	100.00
GJB6	100.00
GLA	100.00
GNAS	100.00
GORAB	100.00
GPR143	89.17
GRHL2	100.00
GSN	97.95
GTF2E2	100.00
GTF2H5	100.00
HAMP	100.00
HCCS	100.00
HDAC8	99.82
HFE	100.00
HJV	100.00
HGD	100.00
HLCS	100.00
HOXC13	96.56
HPGD	99.87
HPS1	100.00
HPS3	99.99
HPS4	99.99
HPS5	100.00
HPS6	96.32
HR	99.78
HRAS	100.00
IFT122	99.99
IFT43	100.00
ELP1	100.00
IKBKG	96.27
IL31RA	100.00
INSR	96.81
ITGA3	99.99
ITGA6	100.00
ITGB4	98.77
JUP	100.00
KANK2	99.99
KCNH1	100.00
KCTD1	100.00
KDM6A	99.63
KDSR	99.98
KIF1A	99.07
KIT	99.98
KITLG	100.00
KL	96.52
KLHL24	100.00
KLLN	100.00
KMT2D	99.99
KRAS	100.00
KREMEN1	92.10
KRT1	99.80
KRT10	99.93
KRT14	100.00
KRT16	99.48
KRT17	92.10
KRT2	100.00
KRT5	100.00
KRT6A	100.00
KRT6B	100.00
KRT6C	99.44
KRT71	99.95
KRT74	99.99
KRT81	100.00
KRT83	99.99
KRT85	99.27
KRT86	99.98
KRT9	100.00
LAMA4	99.75
LAMB3	100.00
LAMC2	99.43
LEMD3	99.97
LIPH	100.00
LIPN	100.00
LMNA	99.52
LMX1B	99.55
LORICRIN	100.00
LPAR6	100.00
LRP1	100.00
LTBP4	99.49
LYST	100.00
LZTR1	99.92
MAP2K1	100.00
MAP2K2	99.99
MAPRE2	100.00
MBTPS2	100.00
MC1R	100.00
MEN1	99.83
MITF	100.00
MLH1	99.99
MLPH	100.00
MMP1	99.99
MMP2	99.93
MPDU1	100.00
MPLKIP	100.00
MSH2	100.00
MSH6	99.92
MSMO1	100.00
MSX1	99.53
MUTYH	100.00
MYO5A	99.78
NF1	98.85
NF2	99.97
NFKBIA	99.97
NGF	100.00
NHP2	100.00
NIPAL4	100.00
NIPBL	99.62
RMRP	100.00
NOP10	100.00
NOTCH1	98.81
NRAS	100.00
NSDHL	100.00
NTRK1	98.91
OCA2	99.73
OFD1	97.68
ORAI1	93.55
OSMR	100.00
PADI3	100.00
PARN	100.00
PAX3	100.00
PDGFRB	100.00
PEX7	96.12
PHYH	99.87
PIGL	100.00
PIK3CA	100.00
PKP1	100.00
PLCD1	99.74
PLEC	99.33
PLOD1	98.77
PLOD3	99.97
PMS2	98.83
PNPLA1	99.66
POFUT1	99.99
POGLUT1	100.00
POLD1	99.84
POLH	100.00
NT5C3A	100.00
PORCN	99.13
PPP1CB	100.00
PRDM12	83.27
PRDM5	100.00
PRKAR1A	100.00
PRKD1	97.12
PSAT1	99.73
PSENEN	100.00
PTCH1	99.03
PTCH2	100.00
PTDSS1	100.00
PTEN	99.64
PTPN11	94.81
NECTIN1	99.68
NECTIN4	99.41
PYCR1	100.00
RAB27A	100.00
RAD21	100.00
RAF1	100.00
RASA2	99.74
RBPJ	99.69
RECQL4	96.90
RET	96.88
RHBDF2	100.00
RIN2	100.00
RIPK4	99.98
RIT1	100.00
RNF113A	100.00
RPL21	84.30
RRAS	98.63
RSPO1	100.00
RTEL1	100.00
SASH1	99.88
SCN11A	99.99
SCN9A	99.99
SDHB	99.35
SDHD	99.95
SEC23B	100.00
SERPINB7	100.00
SERPINB8	100.00
SERPING1	97.68
SETBP1	100.00
SGPL1	100.00
SHOC2	100.00
HHAT	93.18
SKIC2	100.00
SLC24A5	100.00
SLC27A4	99.97
SLC29A3	95.73
SLC2A10	97.06
SLC39A13	100.00
SLC39A4	100.00
SLC45A2	100.00
SLC6A19	99.99
SLURP1	100.00
SMAD3	100.00
SMARCAD1	99.97
SMARCB1	100.00
SMC3	100.00
SMPD1	100.00
SNAI2	100.00
SNAP29	100.00
SNRPE	99.04
SOS1	100.00
SOS2	99.97
SOX10	97.31
SPINK5	100.00
SPRED1	100.00
SPRY1	100.00
SPTLC1	99.44
SRD5A3	98.97
ST14	99.95
STK11	99.81
STS	99.94
SUFU	100.00
SULT2B1	100.00
SUMF1	100.00
TAT	100.00
TCHH	100.00
TERT	93.51
TFR2	100.00
TGFB2	99.97
TGFB3	100.00
TGFBR1	91.97
TGFBR2	100.00
TGM1	100.00
TGM3	100.00
TGM5	100.00
TINF2	99.96
TMC6	99.87
TNXB	100.00
TP63	100.00
TRPS1	100.00
TRPV3	99.99
TSC1	100.00
TSC2	99.99
SKIC3	99.99
TUBB	100.00
TWIST2	99.15
TYR	100.00
TYRP1	100.00
UBR1	100.00
USB1	100.00
UVSSA	100.00
VPS33B	100.00
WDR19	100.00
WDR35	100.00
WNK1	100.00
WNT10A	94.15
WRAP53	100.00
WRN	100.00
XPA	97.89
XPC	100.00
ZMPSTE24	100.00
ZNF469	99.97
ZNF750	100.00
TERC	100.00	t

Intellectual disability/Epilepsy (1091 genes) - ULG

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Comments
A2ML1	99.35	Vissers et al., EJHG 2015 : Noonan syndrome
ABCC9	99.41	Hypertrichotic osteochondrodysplasia
ABCD1	99.49	Adrenoleukodystrophy
ABHD5	98.48	Chanarin-Dorfman syndrome
ACAD9	99.57	Mitochondrial complex I deficiency due to ACAD9 deficiency
ACO2	99.66	Infantile cerebellar-retinal degeneration
ACOX1	99.49	Peroxisomal acyl-CoA oxidase deficiency
ACSL4	91.09	Mental retardation, X-linked 63
ACTB	99.34	Baraitser-Winter syndrome 1
ACTG1	99.69	Baraitser-Winter syndrome 2
ACY1	99.67	Aminoacylase 1 deficiency
ADAR	99.45	Aicardi-Goutieres syndrome 6
ADAT3	81.40	Mental retardation, autosomal recessive 36
ADGRG1	99.67	Polymicrogyria, bilateral frontoparietal
ADK	98.74	Hypermethioninemia due to adenosine kinase deficiency
ADNP	99.55	Helsmoortel-van der Aa syndrome
ADSL	99.58	Adenylosuccinase deficiency
AFF2	90.80	Mental retardation, X-linked, FRAXE type
AGA	99.60	Aspartylglucosaminuria
AGPAT2	91.26	Lipodystrophy, congenital generalized, type 1
AHCY	99.67	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
AHDC1	99.68	Xia-Gibbs syndrome
AHI1	99.05	Joubert syndrome 3
AIMP1	96.88	Leukodystrophy, hypomyelinating, 3
AKT3	98.82	Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2
ALDH18A1	99.66	Cutis laxa, autosomal recessive, type IIIA
ALDH3A2	99.31	Sjogren-Larsson syndrome
ALDH4A1	96.44	Hyperprolinemia, type II
ALDH5A1	93.04	Succinic semialdehyde dehydrogenase deficiency
ALDH7A1	99.00	Epilepsy, pyridoxine-dependent
ALG1	99.43	Congenital disorder of glycosylation, type Ik
ALG11	99.57	Congenital disorder of glycosylation, type Ip
ALG12	99.69	Congenital disorder of glycosylation, type Ig
ALG13	92.88	Epileptic encephalopathy, early infantile, 36
ALG2	97.14	Myasthenic syndrome, congenital, 14, with tubular aggregates
ALG3	99.59	Congenital disorder of glycosylation, type Id
ALG6	98.36	Congenital disorder of glycosylation, type Ic
ALG9	96.33	Gillessen-Kaesbach-Nishimura syndrome
ALMS1	98.27	Alstrom syndrome
ALX1	99.52	Frontonasal dysplasia 3
ALX4	99.07	Frontonasal dysplasia 2
AMER1	99.96	Osteopathia striata with cranial sclerosis
AMPD2	99.69	Pontocerebellar hypoplasia, type 9
AMT	99.69	Glycine encephalopathy
ANK3	99.47	Mental retardation, autosomal recessive, 37
ANKH	99.64	Craniometaphyseal dysplasia
ANKRD11	99.68	KBG syndrome
AP1S1	99.50	MEDNIK syndrome
AP1S2	88.78	Mental retardation, X-linked syndromic 5
AP4B1	99.61	Spastic paraplegia 47, autosomal recessive
AP4M1	99.68	Spastic paraplegia 50, autosomal recessive
AP4S1	99.48	Spastic paraplegia 52, autosomal recessive
APTX	99.02	Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
ARCN1	99.27	Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay
ARFGEF2	99.31	Periventricular heterotopia with microcephaly
ARG1	99.53	Argininemia
ARHGAP31	99.60	Adams-Oliver syndrome 1
ARHGEF2	99.64	Neurodevelopmental disorder with midbrain and hindbrain malformations
ARHGEF9	97.26	Epileptic encephalopathy, early infantile, 8
ARID1A	97.02	Coffin-Siris syndrome 2
ARID1B	97.57	Coffin-Siris syndrome 1
ARID2	99.33	Coffis-Siris syndrome 6
ARL13B	98.36	Joubert syndrome 8
ARL6	99.09	Bardet-Biedl syndrome 3
ARSL	90.38	Chondrodysplasia punctata, X-linked recessive
ARX	65.25	Mental retardation, X-linked 29 and others
ASH1L	99.53	Okamoto et al., AJMG 2017 : MCA/ID syndrome
ASNS	99.42	Asparagine synthetase deficiency
ASPA	99.17	Canavan disease
ASPM	98.50	Microcephaly 5, primary, autosomal recessive
ASXL1	95.03	Bohring-Opitz syndrome
ASXL3	98.20	Bainbridge-Ropers syndrome
ATIC	96.73	AICA-ribosiduria due to ATIC deficiency
ATP6V0A2	99.12	Cutis laxa, autosomal recessive, type IIA
ATP7A	94.32	Menkes disease
ATR	99.17	Seckel syndrome 1
ATRIP	95.19	Ogi et al., PLoS Genet 2012 : Seckel syndrome
ATRX	92.10	Mental retardation-hypotonic facies syndrome, X-linked
AUH	96.75	3-methylglutaconic aciduria, type I
AUTS2	97.55	Mental retardation, autosomal dominant 26
B3GLCT	92.21	Peters-plus syndrome
B4GALT1	98.41	Congenital disorder of glycosylation, type IId
B4GALT7	83.36	Ehlers-Danlos syndrome with short stature and limb anomalies
BBIP1	99.64	Bardet-Biedl syndrome 18
BBS1	99.66	Bardet-Biedl syndrome 1
BBS10	99.57	Bardet-Biedl syndrome 10
BBS12	99.52	Bardet-Biedl syndrome 12
BBS2	99.32	Bardet-Biedl syndrome 2
BBS4	99.49	Bardet-Biedl syndrome 4
BBS5	98.49	Bardet-Biedl syndrome 5
BBS7	99.00	Bardet-Biedl syndrome 7
BBS9	98.68	Bardet-Biedl syndrome 9
BCKDHB	98.82	Maple syrup urine disease, type Ib
BCL11A	99.16	Dias-Logan syndrome
BCOR	96.85	Microphthalmia, syndromic 2
BCS1L	99.69	Leigh syndrome
BLM	99.07	Bloom syndrome
BRAF	94.78	Noonan syndrome 7
BRPF1	99.67	Intellectual developmental disorder with dysmorphic facies and ptosis
BRWD3	93.74	Mental retardation, X-linked 93
BSCL2	99.67	Encephalopathy, progressive, with or without lipodystrophy
BTD	99.68	Biotinidase deficiency
BUB1B	99.40	Mosaic variegated aneuploidy syndrome 1
C12ORF57	99.69	Platzer et al., AJMG 2014 : RM, hypoplasie corps caleux, colobome, Ã©pilepsie.
C19ORF12	99.69	Neurodegeneration with brain iron accumulation 4
C2CD3	99.44	Orofaciodigital syndrome XIV
CPLANE1	98.89	Joubert syndrome 17
CA8	99.19	Cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3
CACNA1A	99.12	Epileptic encephalopathy, early infantile, 42
CACNA1C	99.65	Timothy syndrome
CACNA1D	99.50	Primary aldosteronism, seizures, and neurologic abnormalities
CAMK2A	99.67	Mental retardation, autosomal dominant 53
CAMK2B	96.34	Mental retardation, autosomal dominant 54
CANT1	99.60	Desbuquois dysplasia 1
CASK	95.36	Mental retardation and microcephaly with pontine and cerebellar hypoplasia
CAV1	99.67	Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome
CAVIN1	99.31	Lipodystrophy, congenital generalized, type 4
CBL	99.54	Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia
CBS	99.69	Homocystinuria, B6-responsive and nonresponsive types
CC2D1A	99.64	Mental retardation, autosomal recessive 3
CC2D2A	99.11	Joubert syndrome 9
CCDC22	99.91	Ritscher-Schinzel syndrome 2
CCDC39	98.07	Ciliary dyskinesia, primary, 14
CCDC78	99.69	Myopathy, centronuclear, 4
CCDC88C	99.38	Hydrocephalus, nonsyndromic, autosomal recessive
CD96	99.13	C syndrome
CDC45	99.57	Meier-Gorlin syndrome 7
CDC6	99.32	Meier-Gorlin syndrome 5
CDH15	96.19	Mental retardation, autosomal dominant 3
CDK13	95.39	Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
CDK5RAP2	99.45	Microcephaly 3, primary, autosomal recessive
CDKL5	87.62	Epileptic encephalopathy, early infantile, 2
CDON	98.90	Holoprosencephaly 11
CDT1	89.72	Meier-Gorlin syndrome 4
CENPJ	99.19	Microcephaly 6, primary, autosomal recessive
CEP135	97.81	Microcephaly 8, primary, autosomal recessive
CEP152	98.40	Microcephaly 9, primary, autosomal recessive
CEP290	97.64	Joubert syndrome 5
CEP41	99.07	Joubert syndrome 15
CEP57	99.09	Mosaic variegated aneuploidy syndrome 2
CEP63	99.06	Seckel syndrome 6
CHAMP1	99.63	Mental retardation, autosomal dominant 40
CHAT	97.70	Myasthenic syndrome, congenital, 6, presynaptic
CHD2	99.18	Epileptic encephalopathy, childhood-onset
CHD4	99.65	Sifrim-Hitz-Weiss syndrome
CHD7	99.53	CHARGE syndrome
CHD8	99.58	Autism, susceptibility to, 18
CHKB	97.97	Muscular dystrophy, congenital, megaconial type
CHMP1A	99.59	Pontocerebellar hypoplasia, type 8
CHRNA4	90.96	Epilepsy, nocturnal frontal lobe, 1
CHRND	99.68	Myasthenic syndrome, congenital, 3B, fast-channel
CISD2	98.61	Wolfram syndrome 2
CLCN4	99.27	Mental retardation, X-linked 49/15
CLN3	99.69	Ceroid lipofuscinosis, neuronal, 3
CLN5	97.69	Ceroid lipofuscinosis, neuronal, 5
CLN6	85.06	Ceroid lipofuscinosis, neuronal, 6
CLN8	99.69	Ceroid lipofuscinosis, neuronal, 8
CLP1	99.68	Pontocerebellar hypoplasia, type 10
CLPB	99.62	3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia
CNKSR2	91.50	Houge et al., Mol Syndromol 2012 : ID
CNTNAP2	99.39	Pitt-Hopkins like syndrome 1
COASY	99.68	Neurodegeneration with brain iron accumulation 6
COG1	98.34	Congenital disorder of glycosylation, type IIg
COG5	99.11	Congenital disorder of glycosylation, type IIi
COG6	98.39	Congenital disorder of glycosylation, type IIl
COG7	99.66	Congenital disorder of glycosylation, type IIe
COG8	97.38	Congenital disorder of glycosylation, type IIh
COL4A1	97.86	Porencephaly 1
COL4A2	99.62	Porencephaly 2
CERT1	99.15	Mental retardation, autosomal dominant 34
COLEC10	99.16	Mental retardation, autosomal dominant 34
COLEC11	99.67	3MC syndrome 2
COQ2	94.52	Coenzyme Q10 deficiency, primary, 1
COQ4	98.74	Coenzyme Q10 deficiency, primary, 7
COQ6	99.60	Coenzyme Q10 deficiency, primary, 6
COQ7	99.40	Coenzyme Q10 deficiency, primary, 8
COQ8A	99.69	Coenzyme Q10 deficiency, primary, 4
COQ9	98.23	Coenzyme Q10 deficiency, primary, 5
COX10	99.65	Leigh syndrome due to mitochondrial COX4 deficiency
CRADD	99.63	Mental retardation, autosomal recessive 34, with variant lissencephaly
CRBN	98.86	Mental retardation, autosomal recessive 2
CREBBP	99.62	Rubinstein-Taybi syndrome 1
CSNK2A1	99.32	Okur-Chung neurodevelopmental syndrome
CSPP1	98.95	Joubert syndrome 21
CTC1	99.57	Cerebroretinal microangiopathy with calcifications and cysts
CTCF	99.65	Mental retardation, autosomal dominant 21
CTNNB1	99.65	Mental retardation, autosomal dominant 19
CTSA	99.59	Galactosialidosis
CTSD	94.51	Ceroid lipofuscinosis, neuronal, 10
CUL4B	84.65	Mental retardation, X-linked, syndromic 15 (Cabezas type)
CYB5R3	88.44	Methemoglobinemia, type I
CYP27A1	97.94	Cerebrotendinous xanthomatosis
D2HGDH	98.50	D-2-hydroxyglutaric aciduria
DAG1	99.69	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9
DARS2	99.20	Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
DCAF17	93.81	Woodhouse-Sakati syndrome
DCC	99.55	Mirror movements 1 and/or agenesis of the corpus callosum
DCPS	99.69	Al-Raqad syndrome
DCX	96.94	Lissencephaly, X-linked
DDB2	99.69	Xeroderma pigmentosum, group E, DDB-negative subtype
DDHD2	97.74	Spastic paraplegia 54, autosomal recessive
DDX11	99.66	Warsaw breakage syndrome
DDX3X	96.52	Mental retardation, X-linked 102
DEAF1	92.63	Mental retardation, autosomal dominant 24
DHCR24	99.34	Desmosterolosis
DHCR7	99.68	Smith-Lemli-Opitz syndrome
DHFR	98.50	Megaloblastic anemia due to dihydrofolate reductase deficiency
DHX30	99.51	Lessel et al., AJHG 2017 : global developmental delay (GDD), intellectual disability (ID), severe speech impairment and gait abnormalities.
DIAPH1	95.85	Seizures, cortical blindness, microcephaly syndrome
DKC1	91.60	Dyskeratosis congenita, X-linked
DLD	99.08	Dihydrolipoamide dehydrogenase deficiency
DLG3	98.91	Mental retardation, X-linked 90
DLL4	99.61	Adams-Oliver syndrome 6
DNAJC19	97.60	3-methylglutaconic aciduria, type V
DNM1	96.84	Epileptic encephalopathy, early infantile, 31
DNMT3A	99.69	Tatton-Brown-Rahman syndrome
DNMT3B	99.69	Immunodeficiency-centromeric instability-facial anomalies syndrome 1
DOCK6	97.92	Adams-Oliver syndrome 2
DOCK8	99.24	Hyper-IgE recurrent infection syndrome, autosomal recessive
DPAGT1	99.68	Congenital disorder of glycosylation, type Ij
DPH1	99.67	Developmental delay with short stature, dysmorphic features, and sparse hair
DPM1	99.27	Congenital disorder of glycosylation, type Ie
DPP6	99.57	Mental retardation, autosomal dominant 33
DSCAM	99.29	Wang et al., Nat Commun 2016 : Autisme
DYNC1H1	99.50	Mental retardation, autosomal dominant 13
DYRK1A	99.53	Mental retardation, autosomal dominant 7
EARS2	99.64	Combined oxidative phosphorylation deficiency 12
EBF3	98.59	Hypotonia, ataxia, and delayed development syndrome
EBP	99.89	MEND syndrome
ECHS1	98.49	Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency
EDC3	99.68	Mental retardation, autosomal recessive 50
EEF1A2	88.74	Mental retardation, autosomal dominant 38
EFNB1	99.39	Craniofrontonasal dysplasia
EFTUD2	99.44	Mandibulofacial dysostosis, Guion-Almeida type
EHMT1	95.40	Kleefstra syndrome
EIF2AK3	94.12	Wolcott-Rallison syndrome
EIF2S3	97.88	Mental retardation, X-linked, syndromic, Borck type
ELOVL4	99.45	Ichthyosis, spastic quadriplegia, and mental retardation
ELP2	98.99	Mental retardation, autosomal recessive 58
EML1	96.28	Band heterotopia
EMX2	99.48	Schizencephaly
ENTPD1	99.05	Spastic paraplegia 64, autosomal recessive
EOGT	99.33	Adams-Oliver syndrome 4
EP300	99.56	Rubinstein-Taybi syndrome 2
EPB41L1	99.69	Mental retardation, autosomal dominant 11
EPG5	99.47	Vici syndrome
ERCC2	99.67	Cerebrooculofacioskeletal syndrome 2
ERCC3	99.68	Xeroderma pigmentosum, group B
ERCC4	99.35	Xeroderma pigmentosum, type F/Cockayne syndrome
ERCC5	99.48	Xeroderma pigmentosum, group G/Cockayne syndrome
ERCC6	99.07	Cerebrooculofacioskeletal syndrome 1
ERCC8	99.27	Cockayne syndrome, type A
ERLIN2	99.32	Spastic paraplegia 18, autosomal recessive
ESCO2	98.50	Roberts syndrome
ETHE1	99.60	Ethylmalonic encephalopathy
EXOSC3	99.53	Pontocerebellar hypoplasia, type 1B
EZH2	99.41	Weaver syndrome
EZR	99.63	Riecken et al., Hum Mut 2015 : ID
HYCC1	98.81	Leukodystrophy, hypomyelinating, 5
FARS2	99.56	Combined oxidative phosphorylation deficiency 14
FAT4	99.39	Van Maldergem syndrome 2
FBXL4	99.46	Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)
FBXO31	93.34	Mental retardation, autosomal recessive 45
FGD1	98.23	Mental retardation, X-linked syndromic 16
FGFR1	99.69	Hypogonadotropic hypogonadism 2 with or without anosmia
FGFR2	99.67	Saethre-Chotzen syndrome
FGFR3	95.86	Crouzon syndrome with acanthosis nigricans
FH	99.29	Fumarase deficiency
FKRP	85.03	Muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5
FKTN	99.13	Muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4
FLNA	99.73	Heterotopia, periventricular
FMN2	99.05	Mental retardation, autosomal recessive 47
FMR1	94.48	Fragile X tremor/ataxia syndrome
FOLR1	99.69	Neurodegeneration due to cerebral folate transport deficiency
FOXG1	84.20	Rett syndrome, congenital variant
FOXP1	99.55	Mental retardation with language impairment and with or without autistic features
FOXP2	99.34	Speech-language disorder-1
FOXRED1	99.63	Leigh syndrome due to mitochondrial complex I deficiency
FRAS1	99.57	Fraser syndrome 1
FREM2	99.23	Fraser syndrome 2
FRMPD4	96.56	Mental retardation, X-linked 104
FTCD	95.82	Glutamate formiminotransferase deficiency
FTL	99.55	Neurodegeneration with brain iron accumulation 3
FTO	99.47	Growth retardation, developmental delay, facial dysmorphism
FTSJ1	99.69	Mental retardation, X-linked 9/44
FUCA1	98.18	Fucosidosis
GABRA3	87.08	Niturad et al., Brain 2017 : range of epileptic seizure types, a varying degree of intellectual disability and developmental delay, sometimes with dysmorphic features or nystagmus.
GABRB3	94.66	Epileptic encephalopathy, early infantile, 43
GABRG2	99.57	Epilepsy, generalized, with febrile seizures plus, type 3
GALT	99.68	Galactosemia
GAMT	93.42	Cerebral creatine deficiency syndrome 2
GAN	98.90	Giant axonal neuropathy-1
GATAD2B	99.69	Mental retardation, autosomal dominant 18
GATM	94.01	Cerebral creatine deficiency syndrome 3
GBE1	98.82	Glycogen storage disease IV
GCH1	93.92	Dystonia, DOPA-responsive, with or without hyperphenylalaninemia
GCSH	86.02	Glycine encephalopathy
GDI1	95.21	Mental retardation, X-linked 41
GFAP	99.69	Alexander disease
GJC2	73.70	Leukodystrophy, hypomyelinating, 2
GLB1	99.56	GM1-gangliosidosis, type I
GLDC	97.83	Glycine encephalopathy
GLI2	98.60	Holoprosencephaly 9
GLI3	99.55	Greig cephalopolysyndactyly syndrome
GLUL	99.68	Glutamine deficiency, congenital
GLYCTK	99.69	D-glyceric aciduria
GM2A	99.68	GM2-gangliosidosis, AB variant
GMPPA	99.69	Alacrima, achalasia, and mental retardation syndrome
GMPPB	99.64	Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 14
GNAI3	99.08	Auriculocondylar syndrome 1
GNAO1	99.66	Epileptic encephalopathy, early infantile, 17
GNAS	97.96	Pseudohypoparathyroidism Ia
GNPAT	97.06	Rhizomelic chondrodysplasia punctata, type 2
GNPTAB	99.49	Mucolipidosis II alpha/beta
GNPTG	90.19	Mucolipidosis III gamma
GNS	99.55	Mucopolysaccharidosis type IIID
GPC3	91.66	Simpson-Golabi-Behmel syndrome, type 1
GPHN	99.58	Molybdenum cofactor deficiency C
GPSM2	99.10	Chudley-McCullough syndrome
GPT2	95.20	Mental retardation, autosomal recessive 49
GRIA3	89.99	Mental retardation, X-linked 94
GRID2	99.47	Spinocerebellar ataxia, autosomal recessive 18
GRIK2	99.13	Mental retardation, autosomal recessive, 6
GRIN1	99.54	Mental retardation, autosomal dominant 8
GRIN2A	99.68	Epilepsy, focal, with speech disorder and with or without mental retardation
GRIN2B	99.66	Mental retardation, autosomal dominant 6
GRIP1	99.65	Fraser syndrome 3
GRM1	99.46	Spinocerebellar ataxia 44
GSS	99.59	Glutathione synthetase deficiency
GTF2E2	98.86	Trichothiodystrophy 6, nonphotosensitive
GTF2H5	99.64	Trichothiodystrophy 3, photosensitive
GTPBP3	97.37	Combined oxidative phosphorylation deficiency 23
GUSB	98.73	Mucopolysaccharidosis VII
HACE1	96.37	Spastic paraplegia and psychomotor retardation with or without seizures
HCFC1	99.76	Spastic paraplegia and psychomotor retardation with or without seizures
HCN1	94.14	Epileptic encephalopathy, early infantile, 24
HDAC4	99.68	Fisch et al., AJMG 2016 : ID
HDAC8	99.17	Cornelia de Lange syndrome 5
HECW2	99.50	Neurodevelopmental disorder with hypotonia, seizures, and absent language
HEPACAM	91.30	Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation
HERC1	99.49	Macrocephaly, dysmorphic facies, and psychomotor retardation
HERC2	99.66	Mental retardation, autosomal recessive 38
HESX1	98.36	Growth hormone deficiency with pituitary anomalies
HEXA	99.67	Tay-Sachs disease
HEXB	97.84	Sandhoff disease, infantile, juvenile, and adult forms
HGSNAT	94.00	Mucopolysaccharidosis type IIIC (Sanfilippo C)
HIVEP2	99.60	Mental retardation, autosomal dominant 43
HLCS	99.60	Holocarboxylase synthetase deficiency
HNMT	99.26	Mental retardation, autosomal recessive 51
HNRNPH2	99.85	Mental retardation, X-linked, syndromic, Bain type
HNRNPK	99.17	Au-Kline syndrome
HNRNPU	98.33	Epileptic encephalopathy, early infantile, 54
HOXA1	99.65	Athabaskan brainstem dysgenesis syndrome
HPRT1	75.78	Lesch-Nyhan syndrome
HRAS	99.69	Costello syndrome
HSD17B10	99.97	HSD10 mitochondrial disease
HSPG2	98.62	Dyssegmental dysplasia, Silverman-Handmaker type
HUWE1	97.92	Mental retardation, X-linked syndromic, Turner type
IARS1	99.32	Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy
IARS2	99.11	Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia
IDS	97.07	Mucopolysaccharidosis II
IDUA	77.72	Mucopolysaccharidosis Ih/s
IER3IP1	98.86	Microcephaly, epilepsy, and diabetes syndrome
IFIH1	99.07	Aicardi-Goutieres syndrome 7
IFT172	99.62	Short-rib thoracic dysplasia 10 with or without polydactyly
IFT27	99.69	Bardet-Biedl syndrome 19
IFT57	98.66	Thevenon et al., Clin Genet 2016 : Oro-facial-digital syndrome
IGF1	99.63	Growth retardation with deafness and mental retardation due to IGF1 deficiency
IL1RAPL1	93.86	Mental retardation, X-linked 21/34
INPP5E	98.14	Joubert syndrome 1
INTU	98.49	Bruel et al., JMG 2017 : oro-facial-digital syndrome
IQSEC2	97.05	Mental retardation, X-linked 1/78
IRX5	89.09	Hamamy syndrome
CRPPA	92.51	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
ITGA7	99.67	Muscular dystrophy, congenital, due to ITGA7 deficiency
ITPR1	99.38	Spinocerebellar ataxia 29, congenital nonprogressive
JAM3	99.20	Hemorrhagic destruction of the brain, subependymal calcification, and cataracts
KANSL1	99.63	Koolen-De Vries syndrome
KAT6A	99.60	Mental retardation, autosomal dominant 32
KAT6B	99.21	Genitopatellar syndrome
KCNC1	99.05	Epilepsy, progressive myoclonic 7
KCNC3	76.28	Spinocerebellar ataxia 13
KCNH1	98.56	Temple-Baraitser syndrome
KCNJ10	99.68	SESAME syndrome
KCNJ11	99.69	Diabetes, permanent neonatal, with or without neurologic features
KCNK9	99.67	Birk-Barel mental retardation dysmorphism syndrome
KCNMA1	99.54	Paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy
KCNQ2	98.93	Epileptic encephalopathy, early infantile, 7
KCNQ5	96.45	Mental retardation, autosomal dominant 46
KCNT1	98.70	Epileptic encephalopathy, early infantile, 14
KCTD7	95.20	Epilepsy, progressive myoclonic 3, with or without intracellular inclusions
KDM1A	96.83	Cleft palate, psychomotor retardation, and distinctive facial features
KDM5C	99.87	Mental retardation, X-linked, syndromic, Claes-Jensen type
KDM6A	94.07	Kabuki syndrome 2
KIAA0586	92.34	Joubert syndrome 23
KIAA0753	99.23	Orofaciodigital syndrome XV
NEXMIF	97.66	Mental retardation, X-linked 98
KIF11	98.74	Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
KIF1A	99.66	Mental retardation, autosomal dominant 9
KIFBP	96.44	Goldberg-Shprintzen megacolon syndrome
KIF4A	99.41	Mental retardation, X-linked 100
KIF5A	99.35	Myoclonus, intractable, neonatal
KIF5C	96.19	Cortical dysplasia, complex, with other brain malformations 2
KIF7	99.42	Joubert syndrome 12
KIRREL3	99.66	Mental retardation, autosomal dominant 4
KLC2	99.69	Spastic paraplegia, optic atrophy, and neuropathy
KMT2A	97.93	Wiedemann-Steiner syndrome
KMT2C	99.31	Kleefstra syndrome 2
KMT2D	99.67	Kabuki syndrome 1
KMT2E	98.54	Dong et al., Cell Rep 2014 : trouble du spectre autistique
KMT5B	99.31	Stessman et al., Nat Genet 2017 : autisme et retard dÃ©veloppemental
KNL1	92.70	Microcephaly 4, primary, autosomal recessive
KPTN	99.37	Mental retardation, autosomal recessive 41
KRAS	99.32	Noonan syndrome 3
L1CAM	99.66	CRASH syndrome
L2HGDH	98.45	L-2-hydroxyglutaric aciduria
LAMA1	99.13	Poretti-Boltshauser syndrome
LAMA2	99.46	Muscular dystrophy, congenital, due to partial LAMA2 deficiency
LAMB1	99.50	Lissencephaly 5
LAMC3	97.99	Cortical malformations, occipital
LAMP2	93.32	Danon disease
LARGE1	99.64	Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
LARP7	97.40	Alazami syndrome
LAS1L	99.76	Wilson-Turner syndrome
LIAS	98.94	Hyperglycinemia, lactic acidosis, and seizures
LIG4	99.55	LIG4 syndrome
LINS1	98.65	Mental retardation, autosomal recessive 27
LIPT1	98.69	Lipoyltransferase 1 deficiency
LMBRD1	96.94	Methylmalonic aciduria and homocystinuria, cblF type
LMNA	99.49	Emery-Dreifuss muscular dystrophy 3, AR
LRP2	99.40	Donnai-Barrow syndrome
LZTFL1	98.67	Bardet-Biedl syndrome 17
LZTR1	99.56	Noonan syndrome 10
MAGEL2	98.06	Schaaf-Yang syndrome
MAN1B1	98.88	Mental retardation, autosomal recessive 15
MAN2B1	99.40	Mannosidosis, alpha-, types I and II
MANBA	99.01	Mannosidosis, beta
MAOA	85.51	Brunner syndrome
MAP2K1	99.62	Cardiofaciocutaneous syndrome 3
MAP2K2	99.01	Cardiofaciocutaneous syndrome 4
MASP1	99.59	3MC syndrome 1
MAT1A	99.66	Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency
MBD5	99.52	Mental retardation, autosomal dominant 1
MBOAT7	99.50	Mental retardation, autosomal recessive 57
MBTPS2	96.46	IFAP syndrome with or without BRESHECK syndrome
MCCC1	99.50	3-Methylcrotonyl-CoA carboxylase 1 deficiency
MCOLN1	93.43	Mucolipidosis IV
MCPH1	98.40	Microcephaly 1, primary, autosomal recessive
MECP2	89.77	Rett syndrome
MED12	99.82	Opitz-Kaveggia syndrome
MED13L	99.52	Mental retardation and distinctive facial features with or without cardiac defects
MED17	98.79	Microcephaly, postnatal progressive, with seizures and brain atrophy
MED23	98.87	Mental retardation, autosomal recessive 18
MEF2C	99.52	Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
MEIS2	99.65	Cleft palate, cardiac defects, and mental retardation
METTL23	99.62	Mental retardation, autosomal recessive 44
MFSD8	99.30	Ceroid lipofuscinosis, neuronal, 7
MID1	97.46	Opitz GBBB syndrome, type I
MKKS	99.58	Bardet-Biedl syndrome 6
MKS1	99.54	Bardet-Biedl syndrome 13
MLYCD	87.33	Malonyl-CoA decarboxylase deficiency
MMACHC	99.68	Methylmalonic aciduria and homocystinuria, cblC type
MOCS1	99.68	Molybdenum cofactor deficiency A
MOCS2	99.48	Molybdenum cofactor deficiency B
MOGS	92.25	Congenital disorder of glycosylation, type IIb
MPDU1	99.69	Congenital disorder of glycosylation, type If
MPDZ	99.22	Hydrocephalus, nonsyndromic, autosomal recessive 2
MPLKIP	99.63	Trichothiodystrophy 4, nonphotosensitive
MTFMT	97.00	Combined oxidative phosphorylation deficiency 15
MTHFR	99.58	Homocystinuria due to MTHFR deficiency
MTM1	94.11	Myotubular myopathy, X-linked
MTOR	99.61	Smith-Kingsmore syndrome
MTR	99.55	Homocystinuria-megaloblastic anemia, cblG complementation type
MTRR	99.33	Homocystinuria-megaloblastic anemia, cbl E type
MVK	99.69	Mevalonic aciduria
MYCN	82.91	Feingold syndrome 1
MYO5A	97.60	Griscelli syndrome, type 1
MYT1L	99.59	Mental retardation, autosomal dominant 39
NAA10	87.47	Ogden syndrome
NACC1	99.66	Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination
NAGA	99.67	Schindler disease, type I
NAGLU	84.28	Mucopolysaccharidosis type IIIB (Sanfilippo B)
NALCN	99.38	Congenital contractures of the limbs and face, hypotonia, and developmental delay
NARS2	98.96	Combined oxidative phosphorylation deficiency 24
NBN	98.67	Nijmegen breakage syndrome
NDE1	99.69	Lissencephaly 4 (with microcephaly)
NDP	99.56	Norrie disease
NDST1	99.67	Mental retardation, autosomal recessive 46
NDUFA1	97.69	Mitochondrial complex I deficiency
NDUFA11	99.69	Mitochondrial complex I deficiency
NDUFA12	99.64	Leigh syndrome due to mitochondrial complex 1 deficiency
NDUFA2	99.69	Leigh syndrome due to mitochondrial complex I deficiency
NDUFA9	99.27	Leigh syndrome due to mitochondrial complex I deficiency
NDUFAF6	89.55	Leigh syndrome due to mitochondrial complex I deficiency
NDUFS2	99.25	Mitochondrial complex I deficiency
NDUFS3	99.67	Leigh syndrome due to mitochondrial complex I deficiency
NDUFS4	99.05	Mitochondrial complex I deficiency
NDUFS7	99.38	Leigh syndrome
NEDD4L	98.92	Periventricular nodular heterotopia 7
NFIA	99.44	Brain malformations and urinary tract defects
NFIX	99.64	Sotos syndrome 2
NGF	99.66	Neuropathy, hereditary sensory and autonomic, type V
NHEJ1	99.67	Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation
NHP2	99.64	Dyskeratosis congenita, autosomal recessive 2
NHS	88.25	Nance-Horan syndrome
NIN	99.20	Seckel syndrome 7
NIPBL	98.53	Cornelia de Lange syndrome 1
NKX2-1	92.05	Choreoathetosis, hypothyroidism, and neonatal respiratory distress
NONO	98.37	Mental retardation, X-linked, syndromic 34
NOTCH1	96.74	Adams-Oliver syndrome 5
NPC1	98.34	Niemann-Pick disease, type C1
NPC2	99.67	Niemann-pick disease, type C2
NPHP1	99.24	Joubert syndrome 4
NPHP3	98.15	Meckel syndrome 7
NR2F1	86.66	Bosch-Boonstra-Schaaf optic atrophy syndrome
NR5A1	99.25	Adrenocortical insufficiency
NRAS	99.61	Noonan syndrome 6
NRXN1	99.52	Pitt-Hopkins-like syndrome 2
NSD1	99.26	Sotos syndrome 1
NSDHL	99.39	CHILD syndrome
NSUN2	95.86	Mental retardation, autosomal recessive 5
OCLN	99.47	Pseudo-TORCH syndrome 1
OCRL	92.17	Lowe syndrome
OFD1	92.99	Orofaciodigital syndrome I
OGT	96.41	Mental retardation, X-linked 106
OPHN1	90.64	Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance
ORC1	99.49	Meier-Gorlin syndrome 1
ORC4	98.60	Meier-Gorlin syndrome 2
ORC6	98.10	Meier-Gorlin syndrome 3
OSGEP	99.65	Braun et al., Nat Genet 2017 : Galloway-Mowat syndrome
OTC	92.10	Ornithine transcarbamylase deficiency
OTUD6B	97.03	Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
PACS1	97.17	Schuurs-Hoeijmakers syndrome
PAFAH1B1	98.98	Lissencephaly 1
PAH	99.66	Phenylketonuria
PAK3	87.10	Mental retardation, X-linked 30/47
PANK2	95.75	Neurodegeneration with brain iron accumulation 1
PAX1	82.57	Otofaciocervical syndrome 2
PAX3	99.68	Craniofacial-deafness-hand syndrome
PAX6	99.51	Aniridia
PC	99.69	Pyruvate carboxylase deficiency
PCDH19	99.22	Epileptic encephalopathy, early infantile, 9
PCGF2	99.69	Fitzgerald et al., Nature 2015 : retard mental, retard dÃ©velopemental
PCNT	99.50	Microcephalic osteodysplastic primordial dwarfism, type II
PDE4D	97.76	Acrodysostosis 2, with or without hormone resistance
PDHA1	97.16	Pyruvate dehydrogenase E1-alpha deficiency
PDHB	99.40	Pyruvate dehydrogenase E1-beta deficiency
PDHX	98.49	Lacticacidemia due to PDX1 deficiency
PDSS1	82.84	Coenzyme Q10 deficiency, primary, 2
PDSS2	98.95	Coenzyme Q10 deficiency, primary, 3
PEPD	99.61	Prolidase deficiency
PEX1	98.83	Peroxisome biogenesis disorder 1A (Zellweger)
PEX10	83.86	Peroxisome biogenesis disorder 6A (Zellweger)
PEX11B	99.63	Peroxisome biogenesis disorder 14B
PEX12	99.40	Peroxisome biogenesis disorder 3A (Zellweger)
PEX13	99.25	Peroxisome biogenesis disorder 11A (Zellweger)
PEX14	99.66	Peroxisome biogenesis disorder 13A (Zellweger)
PEX16	99.69	Peroxisome biogenesis disorder 8A (Zellweger)
PEX19	99.60	Peroxisome biogenesis disorder 12A (Zellweger)
PEX2	99.69	Peroxisome biogenesis disorder 5A (Zellweger)
PEX26	96.96	Peroxisome biogenesis disorder 7A (Zellweger)
PEX3	98.89	Peroxisome biogenesis disorder 10A (Zellweger)
PEX5	99.15	Peroxisome biogenesis disorder 2A (Zellweger)
PEX6	98.57	Peroxisome biogenesis disorder 4A (Zellweger)
PEX7	90.36	Peroxisome biogenesis disorder 9B
PGAP1	97.25	Mental retardation, autosomal recessive 42
PGAP2	99.68	Hyperphosphatasia with mental retardation syndrome 3
PGAP3	99.15	Hyperphosphatasia with mental retardation syndrome 4
PGK1	99.16	Phosphoglycerate kinase 1 deficiency
PHC1	99.66	Microcephaly 11, primary, autosomal recessive
PHF6	84.23	Borjeson-Forssman-Lehmann syndrome
PHF8	99.04	Mental retardation syndrome, X-linked, Siderius type
PHGDH	99.67	Phosphoglycerate dehydrogenase deficiency
PHIP	95.93	Webster et al., Cold Spring Harb Mol Case Stud. 2016 : DD, ID, obÃ©sitÃ© et dysmorphies
PIGA	92.30	Multiple congenital anomalies-hypotonia-seizures syndrome 2
PIGG	99.54	Mental retardation, autosomal recessive 53
PIGL	99.59	CHIME syndrome
PIGN	97.78	Multiple congenital anomalies-hypotonia-seizures syndrome 1
PIGO	99.67	Hyperphosphatasia with mental retardation syndrome 2
PIGT	99.63	Multiple congenital anomalies-hypotonia-seizures syndrome 3
PIGV	99.66	Hyperphosphatasia with mental retardation syndrome 1
PIGW	99.68	Hyperphosphatasia with mental retardation syndrome 5
PIGY	99.66	Hyperphosphatasia with mental retardation syndrome 6
PIK3R2	91.70	Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1
PLA2G6	99.69	Neurodegeneration with brain iron accumulation 2B
PLCB1	99.15	Epileptic encephalopathy, early infantile, 12
PLCB4	99.09	Auriculocondylar syndrome 2
PLOD1	98.58	Ehlers-Danlos syndrome, type VI
PLP1	99.86	Pelizaeus-Merzbacher disease
PMM2	98.47	Congenital disorder of glycosylation, type Ia
PNKP	99.68	Microcephaly, seizures, and developmental delay
PNP	99.66	Immunodeficiency due to purine nucleoside phosphorylase deficiency
POC1A	99.26	Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis
POGZ	98.81	White-Sutton syndrome
POLG	99.59	Mitochondrial DNA depletion syndrome 4B (MNGIE type)
POLH	99.55	Xeroderma pigmentosum, variant type
POLR3A	99.40	Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism
POLR3B	99.29	Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism
POMGNT1	99.66	Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3
POMGNT2	99.69	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8
POMK	99.66	Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12
POMT1	99.56	Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1
POMT2	98.42	Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 2
PORCN	99.91	Focal dermal hypoplasia
PPM1D	98.20	Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold
PPP1CB	99.40	Noonan syndrome-like disorder with loose anagen hair 2
PPP2R1A	99.69	Mental retardation, autosomal dominant 36
PPP2R5D	99.64	Mental retardation, autosomal dominant 35
PPT1	99.67	Ceroid lipofuscinosis, neuronal, 1
PQBP1	99.90	Renpenning syndrome
PRICKLE1	99.67	Epilepsy, progressive myoclonic 1B
PRMT7	99.21	Short stature, brachydactyly, intellectual developmental disability, and seizures
PRPS1	98.61	Arts syndrome
PRSS12	98.69	Mental retardation, autosomal recessive 1
PSAP	99.68	Krabbe disease, atypical
PSMD12	99.44	Stankiewicz-Isidor syndrome
PTCH1	97.64	Holoprosencephaly 7
PTCHD1	99.37	Autism, susceptibility to, X-linked 4
PTDSS1	99.56	Lenz-Majewski hyperostotic dwarfism
PTEN	98.68	Cowden syndrome 1
PTPN11	97.30	LEOPARD syndrome 1
PUF60	99.56	Verheij syndrome
PURA	84.89	Mental retardation, autosomal dominant 31
PUS1	93.31	Myopathy, lactic acidosis, and sideroblastic anemia 1
PYCR1	99.67	Cutis laxa, autosomal recessive, type IIB
QDPR	96.67	Hyperphenylalaninemia, BH4-deficient, C
RAB18	98.43	Warburg micro syndrome 3
RAB27A	95.80	Griscelli syndrome, type 2
RAB39B	99.96	Mental retardation, X-linked 72
RAB3GAP1	99.24	Warburg micro syndrome 1
RAB3GAP2	99.14	Martsolf syndrome
RAC1	87.43	Mental retardation, autosomal dominant 48
RAD21	99.34	Cornelia de Lange syndrome 4
RAF1	99.65	Noonan syndrome 5
RAI1	97.85	Smith-Magenis syndrome
RARB	99.52	Microphthalmia, syndromic 12
RARS2	99.20	Pontocerebellar hypoplasia, type 6
RASA2	95.15	Aoki et al., JHG 2016 : RASopathie
RAX	78.51	Microphthalmia, isolated 3
RBBP8	96.69	Seckel syndrome 2
RBM10	99.86	TARP syndrome
RBM28	99.55	Alopecia, neurologic defects, and endocrinopathy syndrome
RBM8A	99.68	Thrombocytopenia-absent radius syndrome
RBPJ	99.36	Adams-Oliver syndrome 3
RECQL4	91.13	Baller-Gerold syndrome
RELN	99.47	Lissencephaly 2 (Norman-Roberts type)
RERE	99.45	Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart
RFT1	97.48	Congenital disorder of glycosylation, type In
RIT1	99.66	Noonan syndrome 8
RMND1	98.79	Combined oxidative phosphorylation deficiency 11
RNASEH2A	99.69	Aicardi-Goutieres syndrome 4
RNASEH2B	90.13	Aicardi-Goutieres syndrome 2
RNASEH2C	96.74	Aicardi-Goutieres syndrome 3
RNASET2	99.45	Leukoencephalopathy, cystic, without megalencephaly
RNF113A	99.85	Trichothiodystrophy 5, nonphotosensitive
ROGDI	90.00	Kohlschutter-Tonz syndrome
RPGRIP1L	95.44	Joubert syndrome 7
RPIA	98.01	Ribose 5-phosphate isomerase deficiency
RPS6KA3	85.79	Coffin-Lowry syndrome
RRAS	94.39	Flex et al., HMG 2014 : RASopathie
RTEL1	99.69	Dyskeratosis congenita, autosomal recessive 5
RTTN	98.71	Microcephaly, short stature, and polymicrogyria with seizures
SALL1	99.68	Townes-Brocks branchiootorenal-like syndrome
SAMHD1	99.47	Aicardi-Goutieres syndrome 5
SATB2	99.46	Glass syndrome
SC5D	99.08	Lathosterolosis
SCN1A	98.95	Epileptic encephalopathy, early infantile, 6 (Dravet syndrome)
SCN2A	98.85	Epileptic encephalopathy, early infantile, 11
SCN8A	99.37	Epileptic encephalopathy, early infantile, 13
SCO2	99.68	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1
SDCCAG8	99.19	Bardet-Biedl syndrome 16
SDHAF1	66.11	Mitochondrial complex II deficiency
SEPSECS	99.07	Pontocerebellar hypoplasia type 2D
SERAC1	98.98	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
SETBP1	98.39	Mental retardation, autosomal dominant 29
SETD2	99.30	Luscan-Lumish syndrome
SETD5	99.55	Mental retardation, autosomal dominant 23
SGSH	96.47	Mucopolysaccharidosis type IIIA (Sanfilippo A)
SHANK2	83.77	Autism susceptibility 17
SHANK3	78.63	Phelan-McDermid syndrome
SHH	90.25	Holoprosencephaly 3
SHOC2	97.89	Noonan-like syndrome with loose anagen hair
SHROOM4	99.52	Stocco dos Santos X-linked mental retardation syndrome
SIL1	99.65	Marinesco-Sjogren syndrome
SIN3A	99.56	Witteveen-Kolk syndrome
SIX3	89.54	Holoprosencephaly 2
SKI	93.23	Shprintzen-Goldberg syndrome
SLC12A6	99.13	Agenesis of the corpus callosum with peripheral neuropathy
SLC16A2	99.71	Allan-Herndon-Dudley syndrome
SLC17A5	98.53	Salla disease
SLC19A3	99.50	Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)
SLC1A4	97.40	Spastic tetraplegia, thin corpus callosum, and progressive microcephaly
SLC25A1	86.05	Combined D-2- and L-2-hydroxyglutaric aciduria
SLC25A12	99.45	Epileptic encephalopathy, early infantile, 39
SLC25A15	99.57	Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome
SLC25A19	99.66	Microcephaly, Amish type
SLC25A22	99.68	Epileptic encephalopathy, early infantile, 3
SLC2A1	93.34	GLUT1 deficiency syndrome 1, infantile onset, severe
SLC33A1	98.70	Congenital cataracts, hearing loss, and neurodegeneration
SLC35A2	99.98	Congenital disorder of glycosylation, type IIm
SLC35C1	99.69	Congenital disorder of glycosylation, type IIc
SLC45A1	92.61	Intellectual developmental disorder with neuropsychiatric features
SLC46A1	97.75	Folate malabsorption, hereditary
SLC4A4	99.23	Renal tubular acidosis, proximal, with ocular abnormalities
SLC6A1	99.61	Myoclonic-atonic epilepsy
SLC6A17	99.68	Mental retardation, autosomal recessive 48
SLC6A3	99.68	Parkinsonism-dystonia, infantile
SLC6A8	92.97	Cerebral creatine deficiency syndrome 1
SLC7A7	99.67	Lysinuric protein intolerance
SLC9A6	80.47	Mental retardation, X-linked syndromic, Christianson type
SMARCA2	97.63	Nicolaides-Baraitser syndrome
SMARCA4	99.68	Coffin-Siris syndrome 4
SMARCB1	99.47	Coffin-Siris syndrome 3
SMARCE1	98.87	Coffin-Siris syndrome 5
SMC1A	97.41	Cornelia de Lange syndrome 2
SMC3	98.62	Cornelia de Lange syndrome 3
SMOC1	98.99	Microphthalmia with limb anomalies
SMPD1	99.68	Niemann-Pick disease, type A
SMS	83.70	Mental retardation, X-linked, Snyder-Robinson type
SNAP29	98.97	Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
SNIP1	99.59	Psychomotor retardation, epilepsy, and craniofacial dysmorphism
SNX14	97.83	Spinocerebellar ataxia, autosomal recessive 20
SOBP	96.13	Mental retardation, anterior maxillary protrusion, and strabismus
SON	99.42	ZTTK syndrome
SOS1	98.22	Noonan syndrome 4
SOS2	98.32	Noonan syndrome 9
SOX10	93.26	Waardenburg syndrome, type 2E, with or without neurologic involvement
SOX11	84.37	Mental retardation, autosomal dominant, 27
SOX2	95.94	Optic nerve hypoplasia and abnormalities of the central nervous system
SOX5	99.56	Lamb-Shaffer syndrome
AFG2A	98.88	Epilepsy, hearing loss, and mental retardation syndrome
SPECC1L	99.49	Opitz GBBB syndrome, type II
SPR	77.10	Dystonia, dopa-responsive, due to sepiapterin reductase deficiency
SPRED1	99.22	Legius syndrome
SPTAN1	99.48	Epileptic encephalopathy, early infantile, 5
SRCAP	99.65	Floating-Harbor syndrome
SRD5A3	96.86	Congenital disorder of glycosylation, type Iq
ST3GAL3	99.66	Mental retardation, autosomal recessive 12
ST3GAL5	85.32	Salt and pepper developmental regression syndrome
STAG1	98.01	Mental retardation, autosomal dominant 47
STAMBP	99.58	Microcephaly-capillary malformation syndrome
STIL	99.24	Microcephaly 7, primary, autosomal recessive
STRA6	99.67	Microphthalmia, syndromic 9
STT3A	99.55	Congenital disorder of glycosylation, type Iw
STT3B	95.54	Congenital disorder of glycosylation, type Ix
STX1B	99.68	Generalized epilepsy with febrile seizures plus, type 9
STXBP1	99.55	Epileptic encephalopathy, early infantile, 4
SUCLG1	98.06	Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)
SUOX	99.68	Sulfite oxidase deficiency
SURF1	86.96	Leigh syndrome, due to COX IV deficiency
SYN1	88.25	Epilepsy, X-linked, with variable learning disabilities and behavior disorders
SYNCRIP	99.45	Lelieveld et al., Nat Neurosci 2016 : ID
SYNE1	99.44	Spinocerebellar ataxia, autosomal recessive 8
SYNGAP1	99.68	Mental retardation, autosomal dominant 5
SYP	93.14	Mental retardation, X-linked 96
SYT14	88.69	Spinocerebellar ataxia, autosomal recessive 11
TAF1	97.05	Mental retardation, X-linked, syndromic 33
TAF2	98.57	Mental retardation, autosomal recessive 40
TBC1D23	97.70	Pontocerebellar hypoplasia, type 11
TBC1D24	99.68	Epileptic encephalopathy, early infantile, 16
TBC1D7	98.94	Macrocephaly/megalencephaly syndrome, autosomal recessive
TBCE	98.41	Hypoparathyroidism-retardation-dysmorphism syndrome
TBCK	98.05	Hypotonia, infantile, with psychomotor retardation and characteristic facies 3
TBL1XR1	98.00	Mental retardation, autosomal dominant 41
TCF20	99.69	SchÃ¤fgen et al., EJHG 2016 : TSA, DI, croissance excessive et hypotonie
TCF4	99.65	Pitt-Hopkins syndrome
TCOF1	99.61	Treacher Collins syndrome 1
TCTN1	99.08	Joubert syndrome 13
TCTN2	99.05	Joubert syndrome 24
TCTN3	99.61	Joubert syndrome 18
TECPR2	99.41	Spastic paraplegia 49, autosomal recessive
TECR	99.69	Mental retardation, autosomal recessive 14
TFAP2A	99.48	Branchiooculofacial syndrome
TGIF1	99.69	Holoprosencephaly 4
TH	98.57	Segawa syndrome, recessive
THOC2	91.08	Mental retardation, X-linked 12/35
THOC6	99.66	Beaulieu-Boycott-Innes syndrome
THRA	99.60	Hypothyroidism, congenital, nongoitrous, 6
TIMM8A	99.66	Mohr-Tranebjaerg syndrome
TINF2	99.67	Dyskeratosis congenita, autosomal dominant 3
TMCO1	95.48	Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
TMEM107	99.69	Orofaciodigital syndrome XVI
TMEM138	99.68	Joubert syndrome 16
TMEM165	87.14	Congenital disorder of glycosylation, type IIk
TMEM216	99.69	Joubert syndrome 2
TMEM231	99.62	Joubert syndrome 20
TMEM237	97.88	Joubert syndrome 14
TMEM67	97.57	Joubert syndrome 6
TMEM70	97.01	Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2
TNK2	99.30	Hitomi et al., Ann Neurol 2013 : severe autosomal recessive infantile-onset epilepsy and ID
TPK1	98.92	Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)
TPP1	99.65	Spinocerebellar ataxia, autosomal recessive 7
TRAPPC11	98.70	Muscular dystrophy, limb-girdle, type 2S
TRAPPC9	99.57	Mental retardation, autosomal recessive 13
TREX1	99.69	Aicardi-Goutieres syndrome 1, dominant and recessive
TRIM32	99.68	Bardet-Biedl syndrome 11
TRIO	97.17	Mental retardation, autosomal dominant 44
TRIP12	99.18	Zhang et al., Hum Gen 2017 : intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
TRMT10A	99.08	Microcephaly, short stature, and impaired glucose metabolism 1
TRMU	94.99	Liver failure, transient infantile
TRPV4	99.64	Spondylometaphyseal dysplasia, Kozlowski type
TSEN2	99.60	Pontocerebellar hypoplasia type 2B
TSEN54	87.28	Pontocerebellar hypoplasia type 2A
TSFM	85.15	Combined oxidative phosphorylation deficiency 3
TSPAN7	98.69	Mental retardation, X-linked 58
SKIC3	99.17	Trichohepatoenteric syndrome 1
TTC8	98.67	Bardet-Biedl syndrome 8
TTI2	99.57	Mental retardation, autosomal recessive 39
TUBA1A	99.69	Lissencephaly 3
TUBA8	97.24	Cortical dysplasia, complex, with other brain malformations 8
TUBB2A	95.11	Cortical dysplasia, complex, with other brain malformations 5
TUBB2B	99.68	Cortical dysplasia, complex, with other brain malformations 7
TUBB3	94.69	Cortical dysplasia, complex, with other brain malformations 1
TUBB4A	98.34	Leukodystrophy, hypomyelinating, 6
TUBG1	99.69	Cortical dysplasia, complex, with other brain malformations 4
TUBGCP6	99.69	Microcephaly and chorioretinopathy, autosomal recessive, 1
TUSC3	99.45	Mental retardation, autosomal recessive 7
TWIST1	59.51	Saethre-Chotzen syndrome
UBE2A	81.32	Mental retardation, X-linked syndromic, Nascimento-type
UBE3A	98.84	Angelman syndrome
UBE3B	99.43	Kaufman oculocerebrofacial syndrome
UBR1	98.99	Johanson-Blizzard syndrome
UNC80	99.46	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2
UPF3B	90.82	Mental retardation, X-linked, syndromic 14
UQCRQ	99.62	Mitochondrial complex III deficiency, nuclear type 4
UROC1	99.69	Urocanase deficiency
USP18	99.69	Pseudo-TORCH syndrome 2
USP9X	93.59	Mental retardation, X-linked 99
VLDLR	97.10	Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1
VPS13B	98.95	Cohen syndrome
VRK1	99.08	Pontocerebellar hypoplasia type 1A
WAC	97.24	Desanto-Shinawi syndrome
WDPCP	98.77	Bardet-Biedl syndrome 15
WDR26	99.46	Skraban-Deardorff syndrome
WDR45	99.94	Neurodegeneration with brain iron accumulation 5
WDR45B	98.84	Suleiman et al., Clin Genet 2017 : intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia
WDR62	99.58	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations
WDR73	99.54	Galloway-Mowat syndrome
WDR81	99.65	Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2
WWOX	99.63	Epileptic encephalopathy, early infantile, 28
XPA	95.49	Xeroderma pigmentosum, group A
XPC	99.66	Xeroderma pigmentosum, group C
XYLT1	91.40	Desbuquois dysplasia 2
YAP1	95.59	Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation
YY1	97.61	Gabriele-de Vries syndrome
ZBTB16	99.69	Skeletal defects, genital hypoplasia, and mental retardation
ZBTB18	99.10	Mental retardation, autosomal dominant 22
ZBTB20	99.63	Primrose syndrome
ZBTB24	99.63	Immunodeficiency-centromeric instability-facial anomalies syndrome-2
ZC4H2	97.81	Wieacker-Wolff syndrome
ZDHHC9	98.90	Mental retardation, X-linked syndromic, Raymond type
ZEB2	99.54	Mowat-Wilson syndrome
ZFYVE26	99.53	Spastic paraplegia 15, autosomal recessive
ZIC2	67.20	Holoprosencephaly 5
ZMPSTE24	98.68	Mandibuloacral dysplasia with type B lipodystrophy
ZMYND11	99.50	Mental retardation, autosomal dominant 30
ZNF335	99.63	Microcephaly 10, primary, autosomal recessive
ZNF41	99.90	Shoichet et al., AJHG 2013 : X-Linked Mental Retardation
ZNF711	89.61	Mental retardation, X-linked 97

Pediatric oncopredisposition - UGent

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Copy number variation
A2ML1	99.97	1
ABCB11	99.86	1
ACD	100.00	1
AIP	99.99	1
ALK	99.93	1
APC	99.97	1
ASXL1	100.00	1
ATM	99.83	1
RNF2	99.99	1
BLM	99.80	1
BMPR1A	99.58	1
BRAF	99.78	1
BRCA1	98.33	1
BRCA2	99.99	1
BRIP1	99.39	1
BUB1B	100.00	1
CBL	99.95	1
CD27	99.95	1
CD70	99.99	1
CDC73	99.60	1
CDH1	99.98	1
CDK4	100.00	1
CDKN1B	100.00	1
CDKN1C	100.00	1
CDKN2A	100.00	1
CEBPA	100.00	1
CEP57	99.92	1
CREBBP	99.97	1
CTC1	100.00	1
CTLA4	99.99	1
CTR9	99.98	1
DDB2	100.00	1
DICER1	99.96	1
DIS3L2	99.90	1
DKC1	99.59	1
DNAJC21	99.67	1
EFL1	99.83	1
EGLN1	99.86	1
EGLN2	99.97	1
ELP1	99.96	1
EPAS1	99.99	1
EPCAM	99.89	1
ERCC2	99.98	1
ERCC3	99.90	1
ERCC4	99.92	1
ERCC5	99.99	1
ERCC6L2	99.94	1
ETV6	99.99	1
EZH2	99.89	1
FANCA	100.00	1
FANCB	99.24	1
FANCC	99.98	1
FANCD2	99.86	1
FANCE	99.99	1
FANCF	100.00	1
FANCG	100.00	1
FANCI	99.96	1
FANCL	99.67	1
FAS	99.99	1
FBXW7	99.90	1
FH	99.95	1
GATA1	99.97	1
GATA2	99.99	1
GPC3	99.60	1
GPC4	99.89	1
GPR161	99.92	1
HAVCR2	99.93	1
HRAS	100.00	1
IKZF1	99.92	1
ITK	99.91	1
KRAS	99.13	1
L2HGDH	99.92	1
LIG4	100.00	1
LZTR1	99.46	1
MAP2K1	99.98	1
MAP2K2	99.99	1
MAX	99.96	1
MDH2	99.54	1
MDM4	99.43	1
MEN1	99.98	1
MLH1	99.64	1
MRAS	99.97	1
MSH2	99.23	1
MSH6	99.97	1
MYSM1	94.16	1
NBN	99.93	1
NF1	99.88	1
NF2	100.00	1
NHP2	99.96	1
NOP10	99.99	1
NRAS	99.66	1
NSD1	99.98	1
PALB2	99.71	1
PARN	99.75	1
PAX5	99.82	1
PHOX2B	99.98	1
PIK3CA	99.74	1
PMS2	70.47	1
POLD1	99.96	1
POLE	99.99	1
POLH	99.85	1
POT1	99.91	1
PPP1CB	99.89	1
PRF1	100.00	1
PRKAR1A	100.00	1
PTCH1	99.99	1
PTEN	99.89	1
PTPN11	99.98	1
RAF1	99.97	1
RB1	99.84	1
RECQL4	100.00	1
REST	99.99	1
RET	99.97	1
RIT1	99.78	1
RMRP	100.00	1
RPL11	99.81	1
RPL15	31.77	1
RPL18	100.00	1
RPL26	30.55	1
RPL27	99.83	1
RPL35	99.99	1
RPL35A	97.55	1
RPL5	28.81	1
RPS10	0.00	1
RPS15A	22.14	1
RPS17	100.00	1
RPS19	100.00	1
RPS24	91.48	1
RPS26	8.99	1
RPS27	27.45	1
RPS28	100.00	1
RPS29	99.96	1
RPS7	88.50	1
RRAS	99.98	1
RRAS2	99.94	1
RTEL1	100.00	1
RUNX1	100.00	1
SAMD9	99.93	1
SAMD9L	99.95	1
SBDS	99.93	1
SDHA	99.98	1
SDHAF2	99.96	1
SDHB	97.32	1
SDHC	99.67	1
SDHD	82.93	1
SETBP1	100.00	1
SH2D1A	98.98	1
SHOC2	99.96	1
SLX4	100.00	1
SMARCA4	99.99	1
SMARCB1	99.99	1
SMARCE1	99.87	1
SOS1	99.68	1
SOS2	99.39	1
SRP72	99.91	1
STK11	100.00	1
SUFU	100.00	1
TERC	98.59	1
TERT	100.00	1
TINF2	100.00	1
TMEM127	99.99	1
TP53	99.98	1
TRIM28	100.00	1
TRIM37	98.19	1
TRIP13	100.00	1
TSC1	99.99	1
TSC2	99.98	1
TSR2	99.96	1
UBE2T	99.89	1
USB1	89.62	1
VHL	100.00	1
WAS	99.90	1
WRAP53	100.00	1
WT1	99.99	1
XPA	99.68	1
XPC	99.98	1
SRP54	99.90	1

Skin disorders - UGent

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Copy number variation
AAAS	99.88	1
AAGAB	100.00	1
ABCA12	99.94	1
ABCB6	99.97	1
ABHD5	99.98	1
ADAM10	99.88	1
ADAR	99.84	1
ADGRE2	98.77	1
ALDH3A2	99.95	1
ALOX12B	100.00	1
ALOXE3	99.98	1
ALX4	100.00	1
ANTXR1	99.83	1
ANTXR2	99.67	1
AP1S1	99.49	1
AP3B1	99.89	1
AP3D1	100.00	1
APCDD1	99.99	1
AQP5	99.88	1
ARHGAP31	100.00	1
ARSL	99.93	1
ATP2A2	99.98	1
ATP6V1B2	99.99	1
ATP7A	99.87	1
AXIN2	100.00	1
BANF1	99.84	1
BCS1L	99.99	1
BLM	99.80	1
BLOC1S3	100.00	1
BLOC1S6	99.98	1
BMS1	85.80	1
BRAF	99.78	1
C1QA	99.99	1
C1QB	99.58	1
C1QC	99.97	1
C5	99.92	1
CARD11	99.97	1
CARD14	99.99	1
CASP10	99.85	1
CASP14	99.86	1
CASP8	99.92	1
CAST	99.94	1
CBL	99.95	1
CD151	100.00	1
CDH1	99.98	1
CDH3	99.98	1
CDKN1B	100.00	1
CDKN1C	100.00	1
CDSN	99.94	1
CERS3	99.85	1
CHST8	100.00	1
CHUK	99.83	1
CLDN1	99.99	1
CLDN10	99.97	1
COG6	99.86	1
COL17A1	99.98	1
COL18A1	99.99	1
COL7A1	99.99	1
COX7B	99.86	1
CYP11B1	100.00	1
CSTB	99.99	1
CSTA	99.83	1
CTLA4	99.99	1
CTSC	99.97	1
CYLD	99.46	1
CYP11A1	99.99	1
CYP21A2	99.85	1
CYP26C1	99.92	1
CYP4F22	99.97	1
DCAF17	99.84	1
DCLRE1C	99.79	1
DCPS	99.98	1
DDB2	100.00	1
DHCR24	99.93	1
DIP2B	99.65	1
DKC1	99.59	1
DLL4	100.00	1
DOCK6	100.00	1
DOCK8	99.86	1
DPH1	100.00	1
DSC3	99.73	1
DSG1	99.35	1
DSG3	99.97	1
DSG4	99.91	1
DSP	100.00	1
DST	99.52	1
DSTYK	99.83	1
DTNBP1	99.89	1
GLB1	99.92	1
EDA	99.44	1
EDAR	99.89	1
EDARADD	99.98	1
EDN3	100.00	1
EDNRA	99.97	1
EDNRB	99.99	1
ELOVL4	99.91	1
ENPP1	99.88	1
EOGT	99.09	1
EPG5	99.95	1
ERCC2	99.98	1
ERCC3	99.90	1
ERCC4	99.92	1
ERCC5	99.99	1
ERCC6	99.60	1
ERCC8	99.79	1
EVC	99.95	1
EVC2	99.97	1
EXPH5	99.81	1
F12	99.99	1
FAM111B	99.98	1
FAS	99.99	1
FASLG	99.84	1
FECH	99.98	1
FERMT1	99.90	1
FGFR1	98.88	1
FGFR3	100.00	1
FOXN1	99.97	1
FZD6	99.95	1
GBA1	96.92	1
GINS1	99.99	1
GJA1	100.00	1
GJB2	100.00	1
GJB3	99.99	1
GJB4	100.00	1
GJB6	100.00	1
GPR143	99.60	1
GREM2	100.00	1
GRHL2	100.00	1
GRIN2B	99.99	1
GTF2E2	100.00	1
GTF2H5	100.00	1
HCCS	99.90	1
HOXC13	99.98	1
HPGD	99.98	1
HPS1	100.00	1
HPS3	99.91	1
HPS4	99.98	1
HPS5	99.91	1
HPS6	100.00	1
HR	99.95	1
HRAS	100.00	1
HSPA9	99.96	1
IFT122	99.98	1
IFT43	99.97	1
IKBKG	57.34	1
IL2RA	99.99	1
IL31RA	100.00	1
ITGA3	99.86	1
ITGA6	99.78	1
ITGB4	99.99	1
ITPR2	99.13	1
JUP	99.94	1
KCNH1	99.92	1
KCTD1	99.99	1
KDF1	99.86	1
KDSR	99.99	1
KEAP1	100.00	1
KIT	99.86	1
KITLG	99.46	1
KLHL24	99.90	1
KRAS	99.13	1
KREMEN1	99.88	1
KRT1	99.89	1
KRT10	100.00	1
KRT13	99.98	1
KRT14	99.99	1
KRT16	100.00	1
KRT17	100.00	1
KRT2	99.88	1
KRT3	99.89	1
KRT5	99.98	1
KRT6A	100.00	1
KRT6B	99.95	1
KRT6C	96.59	1
KRT7	99.87	1
KRT74	99.92	1
KRT83	100.00	1
KRT85	99.97	1
KRT9	100.00	1
LAMA4	99.90	1
LAMB3	99.99	1
LAMC2	99.54	1
LBR	99.66	1
LIPH	99.99	1
LIPN	99.94	1
LMNA	99.96	1
LMNB2	99.99	1
LORICRIN	100.00	1
LPAR6	99.99	1
LRMDA	99.87	1
LRP1	99.94	1
LYST	99.87	1
LZTR1	99.46	1
MBTPS2	99.81	1
MC1R	100.00	1
MC2R	100.00	1
MC4R	100.00	1
MCM4	99.96	1
MEN1	99.98	1
MITF	99.98	1
MLPH	100.00	1
MMP1	99.99	1
MPDU1	99.97	1
MPLKIP	99.99	1
MSX1	100.00	1
MYO5A	99.94	1
NECTIN1	99.99	1
NECTIN4	99.97	1
NF1	99.88	1
NFKBIA	99.99	1
NIPAL4	100.00	1
NLRC4	99.95	1
NLRP1	95.26	1
NLRP12	99.99	1
NLRP3	100.00	1
NNT	99.87	1
NOP10	99.99	1
NOTCH1	99.98	1
NR5A1	99.92	1
NRAS	99.66	1
NSDHL	99.87	1
OCA2	99.60	1
OSMR	99.95	1
PADI3	99.35	1
PAX3	100.00	1
PAX6	99.95	1
PDGFRB	99.99	1
PEPD	99.98	1
PEX7	99.72	1
PGM3	99.94	1
PHGDH	99.79	1
PHYH	100.00	1
PIEZO1	99.98	1
PIGL	99.98	1
PIGT	99.95	1
PKP1	99.98	1
PLCD1	99.98	1
PLCG2	99.99	1
PLEC	100.00	1
PMVK	99.60	1
PNPLA1	99.98	1
PNPLA2	100.00	1
PNPLA6	99.99	1
POFUT1	100.00	1
POGLUT1	99.99	1
POLA1	99.57	1
POLH	99.85	1
POMC	99.99	1
NT5C3A	99.95	1
PORCN	99.93	1
HCRT	99.85	1
PRKCD	99.96	1
PRKD1	99.96	1
PSAT1	99.98	1
PSENEN	100.00	1
PSMB8	99.96	1
PTCH1	99.99	1
PTEN	99.89	1
PTPN11	99.98	1
PTPRF	99.92	1
RAB27A	99.94	1
RAD50	99.75	1
RAF1	99.97	1
RAG1	100.00	1
RAG2	100.00	1
RBM28	99.99	1
RBPJ	99.96	1
RECQL4	100.00	1
RET	99.97	1
RHBDF2	99.95	1
RIN2	99.99	1
RIT1	99.78	1
RMRP	100.00	1
RSPO1	99.99	1
SCN9A	99.83	1
SDR9C7	99.99	1
SERPINB7	99.93	1
SERPINB8	99.98	1
SERPING1	100.00	1
SGPL1	99.95	1
SHOC2	99.96	1
SLC24A5	99.99	1
SLC27A4	100.00	1
SLC29A3	99.98	1
SLC39A4	100.00	1
SLC45A2	100.00	1
SLURP1	100.00	1
SMARCA2	99.95	1
SMARCAD1	99.86	1
SNAI2	100.00	1
SNAP29	99.85	1
SNRPE	99.26	1
SOS1	99.68	1
SOS2	99.39	1
SOX10	100.00	1
SOX18	100.00	1
SPINK5	99.91	1
SPINT1	100.00	1
SPRED1	99.99	1
SRD5A3	99.94	1
ST14	100.00	1
ST3GAL5	99.96	1
STAT3	99.97	1
STIM1	99.99	1
STK11	100.00	1
STS	99.81	1
SULT2B1	99.92	1
SUMF1	99.95	1
TAT	99.99	1
TCHH	99.94	1
TERC	98.59	1
TGM1	99.82	1
TGM3	100.00	1
TGM5	100.00	1
TINF2	100.00	1
TP63	99.97	1
TRPM1	99.96	1
TRPS1	100.00	1
TRPV3	99.90	1
TWIST2	100.00	1
TXNRD2	99.97	1
TYRP1	99.97	1
UBR1	99.93	1
UROD	99.32	1
UROS	100.00	1
USB1	89.62	1
VCX	96.04	1
VCX3A	85.19	1
WDR19	99.80	1
WDR35	99.92	1
WNT10A	100.00	1
XPA	99.68	1
XPC	99.98	1
ZMPSTE24	98.70	1