NOS1AP | Belgian Genetic Tests database

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Name:	nitric oxide synthase 1 adaptor protein
Symbol:	NOS1AP
Version of Orphanet:	2023-06-22 14:14:43
Synonyms:	C-terminal PDZ domain ligand of neuronal nitric oxide synthase CAPON KIAA0464
XREF(s):	Orphanet Ensembl Genatlas HGNC OMIM SwissProt
Created:	13 May 2019 - 01:01
Changed:	22 Jun 2023 - 16:14

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Related Gene Panels

Cardiopathies, hereditary (102 genes) - KUL

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Comments
ABCC9	95.00	NM_005691.4 / interpretable range CS1>95%
ACTC1	95.00	NM_005159.5 / interpretable range CS1>95%
ACTN2	95.00	NM_001103.4 / nterpretable range CS1>95%
AKAP9	95.00	NM_005751.5 /interpretable range CS1>95%
ANK2	95.00	NM_001148.6 / interpretable range CS1>95%
ANKRD1	95.00	NM_014391.3 / interpretable range CS1>95%
BAG3	95.00	NM_004281.4 / interpretable range CS1>95%
CACNA1C	95.00	NM_000719.7 / interpretable range CS1>95%
CACNA1D	95.00	NM_000720.4 / interpretable range CS1>95%
CACNA2D1	95.00	NM_000722.4 / interpretable range CS1>95%
CACNB2	95.00	NM_201590.3 / interpretable range CS1>95%
CALM1	95.00	NM_006888.6 / interpretable range CS1>95%
CALM2	95.00	NM_001743.6 / interpretable range CS1>95%
CALM3	95.00	NM_005184.4 / interpretable range CS1>95%
CALR3	95.00	NM_145046.5 / interpretable range CS1>95%
CASQ2	95.00	NM_001232.4 / interpretable range CS1>95%
CAV3	95.00	NM_033337.3 / interpretable range CS1>95%
CDH2	95.00	NM_001792.5 / interpretable range CS1>95%
CRYAB	95.00	NM_001885.3 / interpretable range CS1>95%
CSRP3	95.00	NM_003476.5 / interpretable range CS1>95%
CTNNA3	95.00	NM_013266.4 / interpretable range CS1>95%
DES	95.00	NM_001927.4 / interpretable range CS1>95%
DSC3	95.00	NM_024422.6 / interpretable range CS1>95%
DSG2	95.00	NM_001943.5 / interpretable range CS1>95%
DSP	95.00	NM_004415.4 / interpretable range CS1>95%
DTNA	95.00	NM_001390.4 / interpretable range CS1>95%
CFH	95.00	NM_001449.5 / interpretable range CS1>95%
FHOD3	95.00	NM_025135.5 / interpretable range CS1>95%
FKTN	95.00	NM_001079802.2 / interpretable range CS1>95%
FLNC	95.00	NM_001458.5 / interpretable range CS1>95%
GJA5	95.00	NM_005266.7 / interpretable range CS1>95%
GLA	95.00	NM_000169.3 / interpretable range CS1>95%
GPD1L	95.00	NM_015141.4 / interpretable range CS1>95%
HCN4	95.00	NM_005477.3 / interpretable range CS1>95%
JPH2	95.00	NM_020433.5 / interpretable range CS1>95%
JUP	95.00	NM_002230.4 / interpretable range CS1>95%
KCNA5	95.00	NM_002234.4 / interpretable range CS1>95%
KCND2	95.00	NM_012281.3 / interpretable range CS1>95%
KCND3	95.00	NM_004980.5 / interpretable range CS1>95%
KCNE1	95.00	NM_000219.6 / interpretable range CS1>95%
KCNE2	95.00	NM_172201.2 / interpretable range CS1>95%
KCNE3	95.00	NM_005472.5 / interpretable range CS1>95%
KCNE5	95.00	NM_012282.4 / interpretable range CS1>95%
KCNH2	95.00	NM_000238.4 / interpretable range CS1>95%
KCNJ2	95.00	NM_000891.3 / interpretable range CS1>95%
KCNJ5	95.00	NM_000890.5 / interpretable range CS1>95%
KCNJ8	95.00	NM_004982.4 / interpretable range CS1>95%
KCNQ1	95.00	NM_000218.3 / interpretable range CS1>95%
LAMA4	95.00	NM_002290.5 / interpretable range CS1>95%
LAMP2	95.00	NM_002294.3 / interpretable range CS1>95%
LDB3	95.00	NM_001080116.1 / interpretable range CS1>95%
LMNA	95.00	NM_170707.4 / interpretable range CS1>95%
MIB1	95.00	NM_020774.4 / interpretable range CS1>95%
MYBPC3	95.00	NM_000256.3 / interpretable range CS1>95% / MLPA only in de frame of "Familial hypertrophic cardiomyopathy"
MYH6	95.00	NM_002471.4 / interpretable range CS1>95%
MYH7	95.00	NM_000257.4 / interpretable range CS1>95%
MYL2	95.00	NM_000432.4 / interpretable range CS1>95%
MYL3	95.00	NM_000258.3 / interpretable range CS1>95%
MYLK2	95.00	NM_033118.4 / interpretable range CS1>95%
MYOZ2	95.00	NM_016599.5 / interpretable range CS1>95%
MYPN	95.00	NM_032578.4 / interpretable range CS1>95%
NEXN	95.00	NM_144573.4 / interpretable range CS1>95%
NKX2-5	95.00	NM_004387.4 / interpretable range CS1>95%
NOS1AP	95.00	NM_014697.3 / interpretable range CS1>95%
NPPA	95.00	NM_006172.4 / interpretable range CS1>95%
NUP155	95.00	NM_153485.3 / interpretable range CS1>95%
PITX2	95.00	NM_153427.2 / interpretable range CS1>95%
PKP2	95.00	NM_004572.4 / interpretable range CS1>95%
PLN	95.00	NM_002667.5 / interpretable range CS1>95%
PRKAG2	95.00	NM_016203.4 / interpretable range CS1>95%
RBM20	95.00	NM_001134363.3 / interpretable range CS1>95%
RYR2	95.00	NM_001035.3 / interpretable range CS1>95%
SLC4A3	95.00	NM_201574.2 / interpretable range CS1>95%
SCN10A	95.00	NM_006514.4 / interpretable range CS1>95%
SCN1B	95.00	NM_001037.5 / interpretable range CS1>95%
SCN2B	95.00	NM_004588.5 / interpretable range CS1>95%
SCN3B	95.00	NM_018400.4 / interpretable range CS1>95%
SCN4B	95.00	NM_174934.4 / interpretable range CS1>95%
SCN5A	95.00	NM_198056.3 / interpretable range CS1>95%
SEMA3A	95.00	NM_006080.3 / interpretable range CS1>95%
SGCD	95.00	NM_000337.6 / interpretable range CS1>95%
SNTA1	95.00	NM_003098.3 / interpretable range CS1>95%
WWTR1	95.00	NM_000116.5 / interpretable range CS1>95%
TBX20	95.00	NM_001077653.2 / interpretable range CS1>95%
TCAP	95.00	NM_003673.4 / interpretable range CS1>95%
TECRL	95.00	NM_001010874.5 / interpretable range CS1>95%
TGFB3	95.00	NM_003239.5 / interpretable range CS1>95%
TJP1	95.00	NM_003257.5 / interpretable range CS1>95%
TMEM43	95.00	NM_024334.3 / interpretable range CS1>95%
TMPO	95.00	NM_003276.2 / interpretable range CS1>95%
TNNI3	95.00	NM_000363.5 / interpretable range CS1>95%
TNNI3K	95.00	NM_015978.3 / interpretable range CS1>95%
TNNT2	95.00	NM_001001430.3 / interpretable range CS1>95%
TPM1	95.00	NM_001018005.2 / interpretable range CS1>95%
TRDN	95.00	NM_006073.4 / interpretable range CS1>95%
TRIM63	95.00	NM_032588.4 / interpretable range CS1>95%
TRPM4	95.00	NM_017636.4 / interpretable range CS1>95%
TTN	95.00	NM_001267550.1 / interpretable range CS1>95%
TTR	95.00	NM_000371.4 / interpretable range CS1>95%
TXNRD2	95.00	NM_006440.5 / interpretable range CS1>95%
VCL	95.00	NM_014000.3 / interpretable range CS1>95%

End-stage renal disease (106 genes) - IPG

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Copy number variation	Comments
ACTN4	100.00	1	NM_004924.6
AGT	100.00	1	NM_001384479.1
AGXT	100.00	1	NM_000030.3
AHI1	100.00	1	NM_001134831.2
ALMS1	100.00	1	NM_001378454.1
ANKFY1	100.00	1	NM_001330063.2
ANLN	100.00	1	NM_018685.5
APOL1	100.00	1	NM_003661.4
APRT	100.00	1	NM_000485.3
ARHGAP24	100.00	1	NM_001025616.3
ARHGDIA	100.00	1	NM_004309.6
AVIL	100.00	1	NM_006576.4
BNC2	100.00	1	NM_017637.6
BSND	100.00	1	NM_057176.3
CC2D2A	100.00	1	NM_001378615.1
CD151	100.00	1	NM_004357.5
CD2AP	100.00	1	NM_012120.3
CEP164	100.00	1	NM_014956.5
CEP290	100.00	1	NM_025114.4
CEP83	100.00	1	NM_016122.3
CFHR5	100.00	1	NM_030787.4
CLCN5	100.00	1	NM_001127898.4
CLCNKA	100.00	1	NM_004070.4
CLCNKB	100.00	1	NM_000085.5
COL4A3	100.00	1	NM_000091.5
COL4A4	100.00	1	NM_000092.5
COL4A5	100.00	1	NM_033380.3
COL4A6	100.00	1	NM_033641.4
COQ8B	100.00	1	NM_024876.4
CPT2	100.00	1	NM_000098.3
CRB2	100.00	1	NM_173689.7
CTNS	100.00	1	NM_004937.3
DCDC2	100.00	1	NM_016356.5
DGKE	100.00	1	NM_003647.3
DNAJB11	100.00	1	NM_016306.6
DSTYK	100.00	1	NM_015375.3
DZIP1L	100.00	1	NM_173543.3
EHHADH	100.00	1	NM_001966.4
EMP2	100.00	1	NM_001424.6
FAN1	100.00	1	NM_014967.5
FN1	100.00	1	NM_212482.4
GANAB	100.00	1	NM_198334.3
GAPVD1	100.00	1	NM_001282680.3
GATM	100.00	1	NM_001482.3
GLIS2	100.00	1	NM_032575.3
GON7	100.00	1	NM_032490.5
GSN	100.00	1	NM_198252.3
HNF1B	100.00	1	NM_000458.4
IFT140	100.00	1	NM_014714.4
IFT43	100.00	1	NM_001102564.3
INF2	100.00	1	NM_022489.4
INVS	100.00	1	NM_014425.5
IQCB1	100.00	1	NM_001023570.4
JAG1	100.00	1	NM_000214.3
LAGE3	100.00	1	NM_006014.5
LAMB2	100.00	1	NM_002292.4
LMX1B	100.00	1	NM_001174147.2
LZTFL1	100.00	1	NM_020347.4
MAGI2	100.00	1	NM_012301.4
MAPKBP1	100.00	1	NM_014994.3
MEFV	100.00	1	NM_000243.3
MMUT	100.00	1	NM_000255.4
MYO1E	100.00	1	NM_004998.4
MYOCD	100.00	1	NM_001146312.3
NDUFAF6	100.00	1	NM_152416.4
NEK8	100.00	1	NM_178170.3
NOS1AP	100.00	1	NM_014697.3
NPHP1	100.00	1	NM_001128178.3
NPHP3	100.00	1	NM_153240.5
NPHP4	100.00	1	NM_015102.5
NPHS1	100.00	1	NM_004646.4
NPHS2	100.00	1	NM_014625.4
NUP107	100.00	1	NM_020401.4
NUP133	100.00	1	NM_018230.3
NUP160	100.00	1	NM_015231.3
NUP205	100.00	1	NM_015135.3
NUP85	100.00	1	NM_024844.5
NUP93	100.00	1	NM_014669.5
OSGEP	100.00	1	NM_017807.4
PAX2	100.00	1	NM_000278.5
PKD1	100.00	1	NM_001009944.3
PKD2	100.00	1	NM_000297.4
PKHD1	100.00	1	NM_138694.4
PLCE1	100.00	1	NM_016341.4
PTPRO	100.00	1	NM_030667.3
RPGRIP1L	96.00	1	NM_015272.5
SDCCAG8	100.00	1	NM_006642.5
SGPL1	100.00	1	NM_003901.4
SLC34A1	100.00	1	NM_003052.5
SLC37A4	100.00	1	NM_001164279.2
SLC41A1	100.00	1	NM_173854.6
SMARCAL1	100.00	1	NM_014140.4
TBC1D8B	100.00	1	NM_017752.3
TMEM231	100.00	1	NM_001077418.3
TMEM67	100.00	1	NM_153704.6
TP53RK	100.00	1	NM_033550.4
TPRKB	100.00	1	NM_016058.5
TRAF3IP1	100.00	1	NM_015650.4
TRPC6	100.00	1	NM_004621.6
TSC1	100.00	1	NM_000368.5
TSC2	100.00	1	NM_000548.5
TTC21B	100.00	1	NM_024753.5
WDR19	100.00	1	NM_025132.4
WT1	100.00	1	NM_024426.6
XPNPEP3	100.00	1	NM_022098.4
YRDC	100.00	1	NM_024640.4

Nephrotic syndrome, FSGS, Alport syndrome (76 genes) - IPG

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Copy number variation	Comments
ACTN4	100.00	1	NM_004924.6
AMN	100.00	1	NM_030943.4
ANLN	100.00	1	NM_018685.5
APOA1	100.00	1	NM_000039.3
APOL1	100.00	1	NM_003661.4
ARHGAP24	100.00	1	NM_001025616.3
ARHGDIA	100.00	1	NM_004309.6
AVIL	100.00	1	NM_006576.4
B2M	100.00	1	NM_004048.4
C3	100.00	1	NM_000064.4
CD151	100.00	1	NM_004357.5
CD2AP	100.00	1	NM_012120.3
CLCN5	100.00	1	NM_001127898.4
COL4A3	100.00	1	NM_000091.5
COL4A4	100.00	1	NM_000092.5
COL4A5	100.00	1	NM_033380.3
COL4A6	100.00	1	NM_033641.4
COQ2	100.00	1	NM_001358921.2
COQ6	100.00	1	NM_182476.3
COQ8A	100.00	1	NM_020247.5
COQ8B	100.00	1	NM_024876.4
CRB2	100.00	1	NM_173689.7
CUBN	100.00	1	NM_001081.4
DGKE	100.00	1	NM_003647.3
EMP2	100.00	1	NM_001424.6
FGA	100.00	1	NM_021871.4
FN1	100.00	1	NM_212482.4
G6PC1	100.00	1	NM_000151.4
GLA	100.00	1	NM_000169.3
GSN	100.00	1	NM_198252.3
INF2	100.00	1	NM_022489.4
KANK2	100.00	1	NM_001136191.3
LAMB2	100.00	1	NM_002292.4
LMX1B	100.00	1	NM_001174147.2
LRP2	100.00	1	NM_004525.3
LYZ	100.00	1	NM_000239.3
MAGI2	100.00	1	NM_012301.4
MYH9	100.00	1	NM_002473.6
MYO1E	100.00	1	NM_004998.4
NPHS1	100.00	1	NM_004646.4
NPHS2	100.00	1	NM_014625.4
NUP107	100.00	1	NM_020401.4
NUP133	100.00	1	NM_018230.3
NUP160	100.00	1	NM_015231.3
NUP205	100.00	1	NM_015135.3
NUP85	100.00	1	NM_024844.5
NUP93	100.00	1	NM_014669.5
OCRL	100.00	1	NM_000276.4
PAX2	100.00	1	NM_000278.5
PDSS2	100.00	1	NM_020381.4
PLCE1	100.00	1	NM_016341.4
PMM2	0.00	1	NM_000303.2 / only position Chr16(GRCh38):g.8797616 87976
PTPRO	100.00	1	NM_030667.3
SGPL1	100.00	1	NM_003901.4
SLC35A1	100.00	1	NM_006416.5
TBC1D8B	100.00	1	NM_017752.3
TRPC6	100.00	1	NM_004621.6
TTC21B	100.00	1	NM_024753.5
TTR	100.00	1	NM_000371.4
UMOD	100.00	1	NM_003361.4
WDR73	100.00	1	NM_032856.5
WT1	100.00	1	NM_024426.6
GON7	100.00	1	NM_032490.5
ITGA3	100.00	1	NM_002204.4
KIRREL1	100.00	1	NM_018240.7
LAGE3	100.00	1	NM_006014.5
LAMA5	100.00	1	NM_005560.6
NOS1AP	100.00	1	NM_014697.3
OSGEP	100.00	1	NM_017807.4
PODXL	94.00	1	NM_001018111.3
SARS2	100.00	1	NM_017827.4
SMARCAL1	100.00	1	NM_014140.4
TP53RK	100.00	1	NM_033550.4
TPRKB	100.00	1	NM_016058.5
WDR4	100.00	1	NM_018669.6
XPO5	100.00	1	NM_020750.3
YRDC	100.00	1	NM_024640.4

Primary Electrical disorders/Brugada syndrome (genepanel) - UZA

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Copy number variation	Comments
ABCB4	100.00	0
ABCC9	100.00	0
ACTN2	100.00	0
AKAP9	100.00	0
ANK2	100.00	0
CACNA1C	100.00	0
CACNA2D1	100.00	0
CACNB2	100.00	0
CALM1	100.00	0
CALM2	100.00	0
CALM3	100.00	0
CASQ2	100.00	0
CAV3	100.00	0
CTNNA3	100.00	0
DES	100.00	0
DPP6	100.00	0
DSC2	100.00	0
DSG2	100.00	0
DSP	100.00	0
GJA1	100.00	0
GJA5	100.00	0
GNB5	100.00	0
GPD1L	100.00	0
HCN4	100.00	0
JUP	100.00	0
KCNA5	100.00	0
KCND3	100.00	0
KCNE1	100.00	0
KCNE2	100.00	0
KCNE3	100.00	0
KCNE5	100.00	0
KCNH2	100.00	0
KCNJ2	100.00	0
KCNJ5	100.00	0
KCNJ8	100.00	0
KCNK17	100.00	0
KCNQ1	100.00	0
LMNA	100.00	0
NKX2-5	100.00	0
NOS1AP	100.00	0
NPPA	100.00	0
PKP2	100.00	0
PLN	100.00	0
PPA2	100.00	0
PRKAG2	100.00	0
RANGRF	100.00	0
RRAD	100.00	0
RYR2	100.00	0
SCN1B	100.00	0
SCN2B	100.00	0
SCN3B	100.00	0
SCN4B	100.00	0
SCN5A	100.00	0
SCN10A	100.00	0
SLMAP	100.00	0
SNTA1	100.00	0
TGFB3	100.00	0
TMEM43	100.00	0
TRDN	100.00	0
TRPM4	100.00	0
CDH2	100.00	0
CLCA2	100.00	0
FLNC	100.00	0
GNB2	100.00	0
MYL3	100.00	0
MYL4	100.00	0
RBM20	100.00	0
RNF207	100.00	0
SLC4A3	100.00	0
TANGO2	100.00	0
TECRL	100.00	0
TNNI3K	100.00	0
TTN	100.00	0

Primary cardiac arrhythmias (113 genes) - VUB

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Comments
ABCC9	100.00	No comment
ACTN2	100.00	No comment
ADRB1	78.34	No comment
ADRB2	100.00	No comment
AGTR1	100.00	No comment
AGXT2	100.00	No comment
AKAP9	100.00	No comment
ALG10B	100.00	No comment
ANK2	100.00	No comment
BAG3	100.00	No comment
CACNA1C	100.00	No comment
CACNA2D1	100.00	No comment
CACNA2D4	99.99	No comment
CACNB2	100.00	No comment
CALM1	100.00	No comment
CALM2	100.00	No comment
CALM3	99.99	No comment
CASQ2	100.00	No comment
CAV3	100.00	No comment
CIT	100.00	No comment
CKMT2	100.00	No comment
CRP	100.00	No comment
CSRP3	100.00	No comment
CTNNA3	100.00	No comment
DEPDC5	99.62	No comment
DPP6	96.95	No comment
DSC3	98.44	No comment
DSG2	99.61	No comment
DSP	100.00	No comment
EMD	99.84	No comment
FGF12	100.00	No comment
GATA4	80.69	No comment
GATA5	97.28	No comment
GATA6	81.11	No comment
GJA5	100.00	No comment
GPD1L	100.00	No comment
HCN4	92.35	No comment
HSPA1L	100.00	No comment
JPH2	95.10	No comment
JUP	100.00	No comment
KCNA5	100.00	No comment
KCNAB2	100.00	No comment
KCNB2	100.00	No comment
KCND3	100.00	No comment
KCNE1	100.00	No comment
KCNE2	100.00	No comment
KCNE3	100.00	No comment
KCNE4	100.00	No comment
KCNE5	94.02	No comment
KCNH2	94.44	No comment
KCNJ16	100.00	No comment
KCNJ2	100.00	No comment
KCNJ5	100.00	No comment
KCNJ8	100.00	No comment
KCNK17	100.00	No comment
KCNK3	95.81	No comment
KCNQ1	91.07	No comment
KCNT1	99.74	No comment
KIF21B	100.00	No comment
LMNA	99.93	No comment
MYBPC3	100.00	No comment
MYH6	100.00	No comment
MYH7	100.00	No comment
MYL4	100.00	No comment
NAA10	96.03	No comment
NKX2-5	100.00	No comment
NKX2-6	100.00	No comment
NOS1AP	100.00	No comment
NPPA	100.00	No comment
NUP155	100.00	No comment
NUP37	100.00	No comment
PI4KA	99.44	No comment
PIK3CG	100.00	No comment
PITX2	100.00	No comment
PKP2	99.87	No comment
PLN	100.00	No comment
PRRX1	100.00	No comment
RANGRF	100.00	No comment
RBM20	99.82	No comment
REM2	100.00	No comment
RIMS1	99.79	No comment
RNF207	99.91	No comment
RYR1	98.38	No comment
RYR2	100.00	No comment
SCN10A	100.00	No comment
SCN1B	94.12	No comment
SCN2B	100.00	No comment
SCN3B	100.00	No comment
SCN4A	100.00	No comment
SCN4B	100.00	No comment
SCN5A	100.00	No comment
SCNN1A	100.00	No comment
SDHAF3	100.00	No comment
SEMA3A	100.00	No comment
SHOX2	99.15	No comment
SIRT6	100.00	No comment
SLC2A5	99.60	No comment
SLC4A3	100.00	No comment
SLMAP	100.00	No comment
SNTA1	84.25	No comment
TBX5	100.00	No comment
TGFB2	100.00	No comment
DDR2	97.72	No comment
TNNI3	100.00	No comment
TPM1	99.98	No comment
TRDN	100.00	No comment
TRPM4	100.00	No comment
TTN	100.00	No comment
UBR4	99.99	No comment
UBR5	100.00	No comment
WDR26	100.00	No comment
XIRP1	100.00	No comment
ZC3HC1	100.00	No comment

cardiopathy panel - UGent

Details

Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Copy number variation
ABCC9	99.92	1
ACADVL	100.00	1
ACTA2	99.99	1
ACTC1	98.57	1
ACTN2	99.99	1
AGL	97.67	1
AKAP10	99.85	1
AKAP9	99.27	1
ALG10	100.00	1
ANK2	99.98	1
ANKRD1	99.57	1
ATP5F1E	100.00	1
BAG3	100.00	1
BRAF	99.78	1
CACNA1C	100.00	1
CACNA2D1	97.12	1
CACNB2	99.93	1
CALM1	99.86	1
CALM2	99.62	1
CALR3	99.91	1
CASQ2	94.39	1
CAV3	100.00	1
CBL	99.95	1
CFC1	21.93	1
CITED2	100.00	1
COA5	98.65	1
CRELD1	99.99	1
CRYAB	100.00	1
CSRP3	100.00	1
CTF1	100.00	1
CTNNA1	99.98	1
CTNNA3	99.96	1
DCHS1	100.00	1
DES	100.00	1
DMD	99.76	1
DMPK	99.93	1
DNM1L	99.40	1
DOLK	100.00	1
DPP6	99.99	1
DSC3	99.73	1
DSG2	99.96	1
DSP	100.00	1
DTNA	100.00	1
ELN	99.86	1
EMD	99.93	1
EYA4	99.96	1
FBN1	99.85	1
FBXO32	99.99	1
CFH	99.97	1
FHL2	100.00	1
FKRP	100.00	1
FKTN	99.94	1
FLNC	99.99	1
FOXRED1	100.00	1
FXN	99.96	1
GAA	100.00	1
GATA4	99.99	1
GATA5	100.00	1
GATA6	99.90	1
GATAD1	99.79	1
GDF1	100.00	1
GJA1	100.00	1
GJA5	100.00	1
GLA	99.90	1
GLB1	100.00	1
GPD1L	99.97	1
GUSB	95.07	1
HAND1	99.99	1
HCN4	100.00	1
HFE	100.00	1
HRAS	100.00	1
ILK	100.00	1
JAG1	100.00	1
JPH2	99.99	1
JUP	99.94	1
KCNA5	100.00	1
KCND3	99.98	1
KCNE1	87.07	1
KCNE2	99.99	1
KCNE3	100.00	1
KCNE5	99.97	1
KCNH2	99.99	1
KCNJ2	100.00	1
KCNJ5	99.99	1
KCNJ8	100.00	1
KCNQ1	100.00	1
KRAS	99.13	1
LAMA4	99.93	1
LAMP2	98.95	1
LDB3	99.91	1
LMNA	99.96	1
MAP2K1	99.98	1
MAP2K2	99.99	1
MED13L	99.99	1
MIB1	99.91	1
MRPL3	99.94	1
MYBPC3	99.98	1
MYH6	100.00	1
MYH7	99.99	1
MYL2	99.99	1
MYL3	99.99	1
MYLK2	100.00	1
MYOM1	99.98	1
MYOZ1	99.93	1
MYOZ2	99.99	1
MYPN	99.88	1
NEBL	99.86	1
NEXN	97.73	1
NKX2-5	99.75	1
NKX2-6	100.00	1
NOS1AP	99.91	1
NPPA	100.00	1
NRAS	99.66	1
PDLIM3	99.94	1
PKP2	94.27	1
PLN	99.97	1
PRKAG2	99.96	1
PSEN1	100.00	1
PSEN2	99.97	1
PTPN11	99.98	1
RAF1	99.97	1
RANGRF	100.00	1
RBM20	99.99	1
RYR2	99.94	1
SCN1B	99.98	1
SCN2B	100.00	1
SCN3B	100.00	1
SCN4B	100.00	1
SCN5A	100.00	1
SCO2	100.00	1
SDHA	99.98	1
SGCD	100.00	1
SHOC2	99.96	1
SLC25A3	99.79	1
SLMAP	99.55	1
SMAD3	99.99	1
SNTA1	99.99	1
SOD2	99.98	1
SOS1	99.68	1
SPRED1	99.99	1
SYNE1	99.95	1
SYNE2	99.95	1
TAFAZZIN	99.98	1
TBX1	99.95	1
TBX20	99.99	1
TCAP	100.00	1
TGFB2	99.87	1
TGFB3	100.00	1
TGFBR1	99.94	1
TGFBR2	99.98	1
TLL1	99.94	1
TMEM43	99.96	1
TMEM70	99.99	1
TMPO	99.81	1
TNNI3	100.00	1
TNNT2	99.87	1
TPM1	99.92	1
TRDN	99.80	1
TRIM63	99.96	1
TRPM4	99.99	1
TSFM	100.00	1
TTN	99.15	1
TTR	100.00	1
TXNRD2	99.97	1
VCL	99.76	1
XK	99.98	1
ZFPM2	100.00	1