Epidermodysplasia Verruciformis(Lewandowsky-Lutz syndrome) Explore Disorder's Alias
An Autosomal recessive mode(s) within the Skin disorders category
Candidate Gene Information
An Autosomal recessive 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 | TMC8/147138 | transmembrane channel like 8 | 17q25.3 | Chr17, NC_000017.11 (78130771..78142968) |
12198 nt | 16 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | TMC6/11322 | transmembrane channel like 6 | 17q25.3 | Chr17, NC_000017.11 (78107397..78132427, complement) |
25031 nt | 23 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 3 | CIB1/10519 | calcium and integrin binding 1 | 15q26.1 | Chr15, NC_000015.10 (90229975..90265759, complement) |
35785 nt | 8 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |