CNGA3 - Gene browser

CNGA3

cyclic nucleotide gated channel subunit alpha 3

HCNC Approved Symbol: CNGA3 (HGNC:2150)
Genomic Coordinates: 2:98,346,456 - 98,398,601 (2q11.2)
Synonyms: CCNC1, CCNCa, CNG3, CNCG3, ACHM2
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

35Patients

In total, 35 patients were diagnosed with a variant in the CNGA3 gene.

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

035
Patient count

Achromatopsia: 13 (37.1%)
Patient Count: 13 (37.1%)
% of total patients presenting each phenotype is shown in parentheses.
13 (37.1%)
Dyschromatopsia: 5 (14.3%)
Patient Count: 5 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
5 (14.3%)
Photophobia: 5 (14.3%)
Patient Count: 5 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
5 (14.3%)
Nystagmus: 4 (11.4%)
Patient Count: 4 (11.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (11.4%)
Cone dystrophy: 4 (11.4%)
Patient Count: 4 (11.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (11.4%)