NOBOX

Gene

NOBOX oogenesis homeobox

HGNCHGNC:22448 EnsemblENSG00000106410 NCBI Gene135935

Locus: gene with protein productLocation: 7q35

Also known as

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

Also known asOG2 · Og2x

View full nomenclature history (3)

Alias symbolsOG2, Og2x

Alias namesnewborn ovary homeobox-encoding gene

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.

Primary Ovarian Insufficiency

Genetic non-acquired premature ovarian failure

Genetic Diseases, Inborn

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.

PRD class homeoboxes and pseudogenes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.