RP1 - Gene browser

RP1

RP1 axonemal microtubule associated

HCNC Approved Symbol: RP1 (HGNC:10263)
Genomic Coordinates: 8:54,559,185 - 54,871,234 (8q11.23-q12.1)
Synonyms: DCDC4A, ORP1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

90Patients

In total, 90 patients were diagnosed with a variant in the RP1 gene.

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

090
Patient count

Retinitis pigmentosa: 41 (45.6%)
Patient Count: 41 (45.6%)
% of total patients presenting each phenotype is shown in parentheses.
41 (45.6%)
Night blindness: 35 (38.9%)
Patient Count: 35 (38.9%)
% of total patients presenting each phenotype is shown in parentheses.
35 (38.9%)
Decreased visual acuity: 34 (37.8%)
Patient Count: 34 (37.8%)
% of total patients presenting each phenotype is shown in parentheses.
34 (37.8%)
Visual impairment: 4 (4.4%)
Patient Count: 4 (4.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (4.4%)
Visual field restriction: 4 (4.4%)
Patient Count: 4 (4.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (4.4%)