Wilms Tumor 1(Wilms tumor, somatic) Explore Disorder's Alias
An Autosomal dominant, Somatic mutation mode(s) within the Cancer disorders category
Candidate Gene Information
An Autosomal dominant, Somatic mutation mode(s) within the Cancer disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | WT1/7490 | WT1 transcription factor | 11p13 | Chr11, NC_000011.10 (32387775..32435539, complement) |
47765 nt | 12 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | BRCA2/675 | BRCA2 DNA repair associated | 13q13.1 | Chr13, NC_000013.11 (32315508..32400268) |
84761 nt | 28 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 3 | GPC3/2719 | glypican 3 | Xq26.2 | ChrX, NC_000023.11 (133535745..133985594, complement) |
449850 nt | 11 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
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