- Diseases
- Idiopathic aplastic anemia
Idiopathic aplastic anemia
Name: |
Idiopathic aplastic anemia
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ORPHAcode: |
88
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Synonyms: |
Idiopathic bone marrow failure
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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Dyskeratosis Congenita (18 genes) - KUL
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ACD 95.00 0 NM_001082486.1/ interpretable range CS1>95% CTC1 95.00 0 NM_025099.5/ interpretable range CS1>95% DKC1 95.00 0 NM_001363.4/ interpretable range CS1>95% GRHL2 95.00 0 NM_024915.3/ interpretable range CS1>95% LIG4 95.00 0 NM_002312.3/ interpretable range CS1>95% TNIP1 95.00 0 NM_138386.2/ interpretable range CS1>95% NHP2 95.00 0 NM_017838.3/ interpretable range CS1>95% NOP10 95.00 0 NM_018648.3/ interpretable range CS1>95% PARN 95.00 0 NM_002582.3/ interpretable range CS1>95% POT1 95.00 0 NM_015450.2/ interpretable range CS1>95% RTEL1 95.00 0 NM_032957.4/ interpretable range CS1>95% STN1 95.00 0 NM_024928.4/ interpretable range CS1>95% TERC 95.00 0 NR_001566.1/ interpretable range CS1>95% TERT 95.00 0 NM_198253.2/ interpretable range CS1>90% TINF2 95.00 0 NM_001099274.1/ interpretable range CS1>95% USB1 95.00 0 NM_024598.3/ interpretable range CS1>95% WRAP53 95.00 0 NM_018081.2/ interpretable range CS1>95% NAF1 95.00 0 NM_138386.3/ interpretable range CS1>95% -
Hematologic Familiar Forms - ULG
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments RPS7 88.11 0 No CHEK2 80.48 0 No PTPN11 95.76 0 No KRAS 96.88 0 No RPS10 98.48 0 No FANCM 97.86 0 No RPL35A 98.16 0 No RPS24 98.39 0 No ANKRD26 100.00 0 Genomic start 27389256 to genomic end 27389427 UTR position RPL5 96.83 0 No SHQ1 97.53 0 No RPS26 98.64 0 No SRP72 97.98 0 No FANCL 98.99 0 No EGLN1 98.71 0 No JAK2 97.81 0 No DNAJC21 98.55 0 No NF1 96.15 0 No BLM 98.77 0 No SBF2 99.19 0 No MSH2 98.36 0 No ATM 98.90 0 No ERCC4 98.33 0 No RPL11 99.02 0 No NBN 99.57 0 No PMS2 98.87 0 No ATG2B 99.33 0 No BRCA2 99.11 0 No ERCC6L2 99.48 0 No ATR 99.19 0 No VPS45 99.60 0 No SRP54 99.44 0 No SBDS 96.51 0 No UBE2T 98.01 0 No RBM8A 99.34 0 No RAD51C 99.83 0 No FANCC 99.72 0 No FANCD2 99.00 0 No BRIP1 99.61 0 No BRCA1 99.80 0 No CEBPA 99.48 0 No PARN 99.84 0 No MSH6 99.84 0 No MECOM 99.83 0 No PALB2 99.80 0 No FANCE 97.83 0 No PAX5 99.72 0 No RAD51 99.94 0 No ATRX 99.85 0 No FANCB 99.61 0 No FANCI 99.66 0 No STN1 99.75 0 No NHP2 99.79 0 No MLH1 99.86 0 No TERT 100.00 0 Genomic start 1295105 to genomic end 1295162 UTR position XRCC2 99.97 0 No FANCA 99.93 0 No EPAS1 99.62 0 No TET2 99.97 0 No HAX1 99.98 0 No SLX4 99.98 0 No CBL 99.87 0 No WAS 99.90 0 No USB1 100.00 0 No EPO 99.99 0 No VHL 99.98 0 No MAD2L2 100.00 0 No RUNX1 99.94 0 No CTC1 99.99 0 No GSKIP 99.99 0 No DKC1 100.00 0 Genomic start 153991031 to genomic end 153991240 UTR position SAMD9L 99.96 0 No MPL 99.99 0 No ETV6 100.00 0 No LIG4 99.98 0 No NOP10 99.99 0 No G6PC3 100.00 0 No CSF3R 100.00 0 No SAMD9 100.00 0 No ELANE 100.00 0 No GATA2 100.00 0 No RPS19 100.00 0 No GFI1 100.00 0 No FANCF 100.00 0 No TPP1 99.99 0 No FANCG 100.00 0 No WRAP53 100.00 0 No TP53 100.00 0 No TINF2 100.00 0 No EPOR 100.00 0 No DDX41 100.00 0 No THPO 100.00 0 No TERC 100.00 0 Genomic start 169482849 to genomic end 169483098 UTR position RTEL1 100.00 0 Genomic start 62326911 to genomic end 62326911 and genomic start 62326900 to genomic end 62326928 and genomic start 62326958 to genomic end 62326986 intronic positions and 99.98 for CDS