WDR19 - Gene browser

WDR19

WD repeat domain 19

HCNC Approved Symbol: WDR19 (HGNC:18340)
Genomic Coordinates: 4:39,182,529 - 39,285,810 (4p14)
Synonyms: Pwdmp, KIAA1638, FLJ23127, ORF26, DYF-2, Oseg6, IFT144, NPHP13, FAP66, CFAP66
Disease Associations: This gene is associated with the following 5 diseases in OMIM.

12Patients

In total, 12 patients were diagnosed with a variant in the WDR19 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

012
Patient count

Retinitis pigmentosa: 5 (41.7%)
Patient Count: 5 (41.7%)
% of total patients presenting each phenotype is shown in parentheses.
5 (41.7%)
Stage 5 chronic kidney disease: 3 (25.0%)
Patient Count: 3 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (25.0%)
Intellectual disability: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Chronic kidney disease: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Retinal dystrophy: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)