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SLC13A5

solute carrier family 13 member 5
2 disorders 2 causative 17p13.1 gene with protein product
HGNC:23089MonarchNCBI Gene 284111ENSG00000141485UniProt Q86YT5OMIM 608305

Aliases: NACT, INDY, mINDY.

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
SLC13A5 Citrate Transporter Disorder causative germline
Undetermined Early-Onset Epileptic Encephalopathy causative germline
mechanism: Early developmental brain network dysfunction
subtype: DEE25
scoped to subtype: DEE25

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