CNGA1 - Gene browser

CNGA1

cyclic nucleotide gated channel subunit alpha 1

HCNC Approved Symbol: CNGA1 (HGNC:2148)
Genomic Coordinates: 4:47,935,977 - 48,016,681 (4p12)
Synonyms: RCNC1, RCNCa, CNG1, RP49, CNCG1, CNCG
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

19Patients

In total, 19 patients were diagnosed with a variant in the CNGA1 gene.

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

019
Patient count

Retinitis pigmentosa: 9 (47.4%)
Patient Count: 9 (47.4%)
% of total patients presenting each phenotype is shown in parentheses.
9 (47.4%)
Night blindness: 5 (26.3%)
Patient Count: 5 (26.3%)
% of total patients presenting each phenotype is shown in parentheses.
5 (26.3%)
Decreased visual acuity: 4 (21.1%)
Patient Count: 4 (21.1%)
% of total patients presenting each phenotype is shown in parentheses.
4 (21.1%)
Hearing impairment: 2 (10.5%)
Patient Count: 2 (10.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (10.5%)
Pericentral retinitis pigmentosa: 2 (10.5%)
Patient Count: 2 (10.5%)
% of total patients presenting each phenotype is shown in parentheses.
2 (10.5%)