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NR0B1

Gene

nuclear receptor subfamily 0 group B member 1

HGNCHGNC:7960EnsemblENSG00000169297NCBI Gene190
Locus: gene with protein productLocation: Xp21.2

Also known as

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

Also known asDSS · AHC · AHCH · DAX1
View full nomenclature history (6)
Previous symbolsDSS, AHC
Alias symbolsAHCH, DAX1
Previous namesdosage-sensitive sex reversal, nuclear receptor subfamily 0, group B, member 1

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.

Neurodegenerative Diseases
Alternating hemiplegia of childhood
Genetic Diseases, Inborn
Carcinoma, Hepatocellular
Prostate carcinoma

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.

Nuclear receptor subfamily 0 group B

Provenance

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