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GJA3

gap junction protein alpha 3

HCNC Approved Symbol
GJA3 (HGNC:4277)
Genomic Coordinates
13:20,138,255 - 20,161,565 (13q12.11)
Synonyms
CX46, CZP3
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the GJA3 gene.

Frequently observed phenotypes

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

Congenital cataracts
 1 (50.0%)
Microcornea
 1 (50.0%)
Nystagmus
 1 (50.0%)
Abnormal temper tantrums
 1 (50.0%)
Cataract
 1 (50.0%)
GJA3 - Gene browser | 3billion