SLC24A1 - Gene browser

SLC24A1

solute carrier family 24 member 1

HCNC Approved Symbol: SLC24A1 (HGNC:10975)
Genomic Coordinates: 15:65,611,350 - 65,661,002 (15q22.31)
Synonyms: NCKX1, NCKX, RODX, KIAA0702, HsT17412, CSNB1D
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

7Patients

In total, 7 patients were diagnosed with a variant in the SLC24A1 gene.

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

07
Patient count

Retinitis pigmentosa: 3 (42.9%)
Patient Count: 3 (42.9%)
% of total patients presenting each phenotype is shown in parentheses.
3 (42.9%)
Poor night vision: 1 (14.3%)
Patient Count: 1 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (14.3%)
Limited peripheral vision: 1 (14.3%)
Patient Count: 1 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (14.3%)
Nyctalopia: 1 (14.3%)
Patient Count: 1 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (14.3%)
Abnormal retinal morphology: 1 (14.3%)
Patient Count: 1 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (14.3%)