SP2

Gene

Sp2 transcription factor

HGNCHGNC:11207 EnsemblENSG00000167182 NCBI Gene6668

Locus: gene with protein productLocation: 17q21.32

Also known as

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

Also known asKIAA0048

View full nomenclature history (1)

Alias symbolsKIAA0048

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.

Hair color

Carcinoma, Squamous Cell

Pre-Eclampsia

Acute Kidney Injury

Carcinoma, Hepatocellular

Nasopharyngeal Carcinoma

Central Nervous System Neoplasms

Glioma

Diabetes Mellitus, Type 1

Neoplasms

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.

Zinc fingers C2H2-typeSp transcription factors

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.