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SLC27A4

solute carrier family 27 member 4
2 disorders 1 causative 1 no genetic record 9q34.11 gene with protein product
HGNC:10998MonarchNCBI Gene 10999ENSG00000167114UniProt Q6P1M0OMIM 604194

Aliases: FATP4, ACSVL4, FATP-4.

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
Ichthyosis Prematurity Syndrome causative germline loss of function
mechanism: FATP4 Acyl-CoA Synthetase Deficiency
Type 2 Diabetes Mellitus no genetic record
mechanism: Insulin-Stimulated Adipocyte Fatty Acid Uptake via FATP1
Mechanism modules · computed from kb/

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