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GFI1B

Gene

growth factor independent 1B transcriptional repressor

HGNCHGNC:4238EnsemblENSG00000165702NCBI Gene8328
Locus: gene with protein productLocation: 9q34.13

Also known as

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

Also known asZNF163B
View full nomenclature history (2)
Alias symbolsZNF163B
Previous namesgrowth factor independent 1B (potential regulator of CDKN1A, translocated in CML)

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.

Genetic Diseases, Inborn
Autosomal dominant macrothrombocytopenia
Alzheimer's Disease

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-typeSNAG transcriptional repressorsMicroRNA protein coding host genes

Provenance

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