Van Der Woude Syndrome 1(IRF6-Related disorders) Explore Disorder's Alias
An Autosomal dominant mode(s) within the Oral disorders category
Candidate Gene Information
An Autosomal dominant mode(s) within the Oral 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 | IRF6/3664 | interferon regulatory factor 6 | 1q32.2 | Chr1, NC_000001.11 (209785617..209806142, complement) |
20526 nt | 9 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | GRHL3/57822 | grainyhead like transcription factor 3 | 1p36.11 | Chr1, NC_000001.11 (24319357..24364482) |
45126 nt | 19 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |