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SLC24A5

solute carrier family 24 member 5

HCNC Approved Symbol
SLC24A5 (HGNC:20611)
Genomic Coordinates
15:48,120,990 - 48,142,672 (15q21.1)
Synonyms
JSX, OCA6, NCKX5
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
[Skin/hair/eye pigmentation 4, fair/dark skin]
113750AR
Albinism, oculocutaneous, type VI
113750AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC24A5 gene.

Frequently observed phenotypes

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

No Results