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CHD2

Gene

chromodomain helicase DNA binding protein 2

HGNCHGNC:1917EnsemblENSG00000173575NCBI Gene1106
Locus: gene with protein productLocation: 15q26.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asFLJ38614 · DKFZp547I1315 · DKFZp781D1727 · DKFZp686E01200
View full nomenclature history (4)
Alias symbolsFLJ38614, DKFZp547I1315, DKFZp781D1727, DKFZp686E01200

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Leukemia, Lymphocytic, Chronic, B-Cell
Complex neurodevelopmental disorder
Leukemia, Lymphoid
Genetic Diseases, Inborn
Neurodegenerative Diseases

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

HelicasesSNF2 related familyMicroRNA protein coding host genes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.