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SLC45A2

solute carrier family 45 member 2
2 disorders 1 untyped 1 susceptibility 5p13.2 gene with protein product
HGNC:16472MonarchNCBI Gene 51151ENSG00000164175UniProt Q9UMX9OMIM 606202

Previous symbols: MATP. Aliases: AIM-1, OCA4.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Rosacea susceptibility
Oculocutaneous Albinism untyped
Causative
mechanism: Melanosomal Ion Transport and pH Dysregulation
subtype: OCA4
scoped to subtype: OCA4

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.