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NSFL1C

Gene

NSFL1 cofactor

HGNCHGNC:15912EnsemblENSG00000088833NCBI Gene55968
Locus: gene with protein productLocation: 20p13

Also known as

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

Also known asdJ776F14.1 · p47 · UBXD10 · UBX1 · UBXN2C
View full nomenclature history (8)
Alias symbolsdJ776F14.1, p47, UBXD10, UBX1, UBXN2C
Previous namesNSFL1 (p97) cofactor (p47)
Alias namesSHP1 homolog (S. cerevisiae), UBX domain protein 2C

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
Familial prostate cancer
Lymphoma
Neoplasms
Prostate carcinoma
Prostate neoplasm
Prostatic 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.

UBX domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.