SEMA4A - Gene browser | 3billion

SEMA4A

SEMA4A

semaphorin 4A

HCNC Approved Symbol: SEMA4A (HGNC:10729)
Genomic Coordinates: 1:156,147,373 - 156,177,744 (1q22)
Synonyms: SemB, FLJ12287, CORD10, SEMAB
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the SEMA4A gene.

Frequently observed phenotypes(Top 5 only)

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

02
Patient count

Cone rod dystrophy: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Retinitis pigmentosa: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)

Last updated: 2024-06-30

SEMA4A - Gene browser | 3billion