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FAAP100

Gene

FA core complex associated protein 100

HGNCHGNC:26171EnsemblENSG00000185504NCBI Gene80233
Locus: gene with protein productLocation: 17q25.3

Also known as

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

Also known asC17orf70 · FLJ22175
View full nomenclature history (5)
Previous symbolsC17orf70
Alias symbolsFLJ22175
Previous nameschromosome 17 open reading frame 70, Fanconi anemia core complex associated protein 100
Alias namesFanconi anemia-associated protein, 100kDa

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.

Fanconi Anemia
46,XX gonadal dysgenesis
Primary Ovarian Insufficiency
Spermatogenic failure
Friedreich Ataxia
Non-syndromic male infertility due to sperm motility disorder

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.

FA core complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-10-07.
Open TargetsGene–disease associations from the Open Targets Platform.