WFS1 - Gene browser

WFS1

wolframin ER transmembrane glycoprotein

HCNC Approved Symbol: WFS1 (HGNC:12762)
Genomic Coordinates: 4:6,269,850 - 6,303,265 (4p16.1)
Synonyms: DIDMOAD, WFS, DFNA6, DFNA14, DFNA38
Disease Associations: This gene is associated with the following 5 diseases in OMIM.

30Patients

In total, 30 patients were diagnosed with a variant in the WFS1 gene.

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

030
Patient count

Hearing loss: 9 (30.0%)
Patient Count: 9 (30.0%)
% of total patients presenting each phenotype is shown in parentheses.
9 (30.0%)
Diabetes mellitus: 6 (20.0%)
Patient Count: 6 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
6 (20.0%)
Optic atrophy: 5 (16.7%)
Patient Count: 5 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
5 (16.7%)
Deafness: 3 (10.0%)
Patient Count: 3 (10.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (10.0%)
Dyschromatopsia: 2 (6.7%)
Patient Count: 2 (6.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (6.7%)