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SLC24A4

solute carrier family 24 member 4

HCNC Approved Symbol
SLC24A4 (HGNC:10978)
Genomic Coordinates
14:92,322,581 - 92,501,481 (14q32.12)
Synonyms
NCKX4
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
[Skin/hair/eye pigmentation 6, blond/brown hair]
210750AR
[Skin/hair/eye pigmentation 6, blue/green eyes]
210750AR
Amelogenesis imperfecta, type IIA5
615887AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC24A4 gene.

Frequently observed phenotypes

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

No Results