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MIS18BP1

Gene

MIS18 binding protein 1

HGNCHGNC:20190EnsemblENSG00000129534NCBI Gene55320
Locus: gene with protein productLocation: 14q21.2

Also known as

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

Also known asC14orf106 · KIAA1903 · M18BP1 · FLJ11186 · KNL2
View full nomenclature history (7)
Previous symbolsC14orf106
Alias symbolsKIAA1903, M18BP1, FLJ11186, KNL2
Previous nameschromosome 14 open reading frame 106
Alias nameskinetochore null 2 homolog (C. elegans)

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
Ovarian dysfunction
Joint Diseases
Central Nervous System Infections
Disorders of Excessive Somnolence
Psoriasis
Glomerulonephritis, IGA

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.

Myb/SANT domain containing

Provenance

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