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CHD7

Gene

chromodomain helicase DNA binding protein 7

HGNCHGNC:20626EnsemblENSG00000171316NCBI Gene55636
Locus: gene with protein productLocation: 8q12.2

Also known as

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

Also known asCRG · KIAA1416 · FLJ20357 · FLJ20361
View full nomenclature history (5)
Previous symbolsCRG
Alias symbolsKIAA1416, FLJ20357, FLJ20361
Previous namesCHARGE association

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.

Hypogonadism
Kallmann syndrome
Genetic Diseases, Inborn
Neurodegenerative Diseases
Immune System 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.

Myb/SANT domain containingHelicasesSNF2 related family

Provenance

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