Search for a gene
WDR19 - WD repeat domain 19
- Synonym(s) : DYF-2, FAP66, FLJ23127, IFT144, intraflagellar transport 144 homolog (Chlamydomonas), KIAA1638, NPHP13, ORF26, Oseg6, Pwdmp
- Previous symbols and names : _
- Type : gene with protein product
- Chromosomal location : 4p14
- OMIM: 608151
- HGNC: 18340
- UniProtKB: Q8NEZ3
- Genatlas: WDR19
- GenCC: WDR19
- Ensembl: ENSG00000157796
- IUPHAR-DB: -
- Reactome: Q8NEZ3
- LOVD: WDR19
Diseases list
- Disease-causing germline mutation(s) in Cranioectodermal dysplasia
ORPHA:1515 - Disease-causing germline mutation(s) in Jeune syndrome
ORPHA:474 - Disease-causing germline mutation(s) in Juvenile nephronophthisis
ORPHA:93592 - Disease-causing germline mutation(s) in Senior-Loken syndrome
ORPHA:3156

Additional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.