SLC19A2

solute carrier family 19 member 2

2 disorders 1 untyped 1 causative 1q24.2 gene with protein product

HGNC:10938 Monarch NCBI Gene 10560 ENSG00000117479 UniProt O60779 OMIM 603941

Previous symbols: TRMA. Aliases: THTR1, ThT1.

Normal function · from ai-gene-review (O60779, commit 79fe13b38970) · AI-generated, not KB evidence

ai-gene-review has this gene at status INITIALIZED; the description is shown only once the review is complete. Read the draft upstream.

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.

Disorder	Relationship	Where the gene appears
Thiamine-Responsive Megaloblastic Anemia Syndrome	causative
Diabetes mellitus	untyped Causative	mechanism: Monogenic Beta-Cell Dysfunction scoped to subtype: monogenic diabetes

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