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DALRD3

DALR anticodon binding domain containing 3
2 disorders 1 causative 1 untyped 3p21.31 gene with protein product
HGNC:25536MonarchNCBI Gene 55152ENSG00000178149UniProt Q5D0E6OMIM 618904

Aliases: FLJ10496.

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
Genetic Developmental and Epileptic Encephalopathy causative
mechanism: Genetic Lesion Beyond the Channelopathies
subtype: DEE86
scoped to subtype: DEE86
Obsessive-Compulsive Disorder untyped
Risk Factor

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