POC1B - Gene browser

POC1B

POC1 centriolar protein B

HCNC Approved Symbol: POC1B (HGNC:30836)
Genomic Coordinates: 12:89,419,718 - 89,526,047 (12q21.33)
Synonyms: TUWD12, FLJ14923, WDR51B
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

10Patients

In total, 10 patients were diagnosed with a variant in the POC1B gene.

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

010
Patient count

Photophobia: 5 (50.0%)
Patient Count: 5 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
5 (50.0%)
Night blindness: 4 (40.0%)
Patient Count: 4 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (40.0%)
Cone dystrophy: 4 (40.0%)
Patient Count: 4 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (40.0%)
Retinal dystrophy: 4 (40.0%)
Patient Count: 4 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
4 (40.0%)
Decreased visual acuity: 3 (30.0%)
Patient Count: 3 (30.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (30.0%)