SETD1A

SET domain containing 1A, histone lysine methyltransferase

3 disorders 1 susceptibility 1 risk factor 1 causative 16p11.2 gene with protein product

HGNC:29010 Monarch NCBI Gene 9739 ENSG00000099381 UniProt O15047 OMIM 611052

Aliases: KIAA0339, Set1, KMT2F, SET1A.

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
Bipolar Disorder	susceptibility
Schizophrenia	risk factor
SETD1A-Related Early-Onset Epilepsy	causative de novo loss of function	mechanism: SETD1A Haploinsufficiency

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