CNGB1 - Gene browser

CNGB1

cyclic nucleotide gated channel subunit beta 1

HCNC Approved Symbol: CNGB1 (HGNC:2151)
Genomic Coordinates: 16:57,882,340 - 57,971,128 (16q21)
Synonyms: RCNC2, RCNCb, GARP, GAR1, CNGB1B, RP45, CNCG2, CNCG3L
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

45Patients

In total, 45 patients were diagnosed with a variant in the CNGB1 gene.

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

045
Patient count

Retinitis pigmentosa: 27 (60.0%)
Patient Count: 27 (60.0%)
% of total patients presenting each phenotype is shown in parentheses.
27 (60.0%)
Night blindness: 8 (17.8%)
Patient Count: 8 (17.8%)
% of total patients presenting each phenotype is shown in parentheses.
8 (17.8%)
Decreased visual acuity: 6 (13.3%)
Patient Count: 6 (13.3%)
% of total patients presenting each phenotype is shown in parentheses.
6 (13.3%)
Visual impairment: 4 (8.9%)
Patient Count: 4 (8.9%)
% of total patients presenting each phenotype is shown in parentheses.
4 (8.9%)
Retinal disease: 3 (6.7%)
Patient Count: 3 (6.7%)
% of total patients presenting each phenotype is shown in parentheses.
3 (6.7%)