Vitiligo
An Unknown mode(s) within the Skin disorders category
Candidate Gene Information
An Unknown mode(s) within the Skin 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 | PTPN2/5771 | protein tyrosine phosphatase non-receptor type 2 | 18p11.21 | Chr18, NC_000018.10 (12785478..12884237, complement) |
98760 nt | 15 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | NLRP1/22861 | NLR family pyrin domain containing 1 | 17p13.2 | Chr17, NC_000017.11 (5501396..5584509, complement) |
83114 nt | 18 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 3 | MTHFR/4524 | methylenetetrahydrofolate reductase | 1p36.22 | Chr1, NC_000001.11 (11785723..11805964, complement) |
20242 nt | 13 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: GTR MalaCards NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities