Browse All / Genes / DGCR8

DGCR8

DGCR8 microprocessor complex subunit
2 disorders 1 no genetic record 1 untyped 22q11.21 gene with protein product
HGNC:2847MonarchNCBI Gene 54487ENSG00000128191UniProt Q8WYQ5OMIM 609030

Previous symbols: C22orf12. Aliases: DGCRK6, Gy1, pasha.

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
Pineoblastoma untyped
Somatic Alterations
mechanism: MicroRNA-Processing Pathway Inactivation
subtype: PB-miRNA2
22q11.2 Deletion Syndrome no genetic record
mechanism: DGCR8-associated miRNA-processing disruption; Recurrent LCR22-mediated multigene deletion

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