Terminology Service for NFDI4Health

FANCG Gene

Go to external page http://purl.obolibrary.org/obo/NCIT_C24385


This gene is involved in the maintenance of genomic integrity and nuclear signal transduction. Allelic variants of the gene are involved in Fanconi syndrome. [ ]

Term info

Label

FANCG Gene

Synonyms
  • FA Complementation Group G Gene
  • FANCG
  • FANCG Gene
Subsets

NCIT_C116977, NCIT_C142801, NCIT_C142800, NCIT_C142799

Display Name

FANCG Gene

HGNC ID

HGNC:3588

Legacy Concept Name

FANCG_Gene

Maps To

FANCG

OMIM Number

602956

Preferred Name

FANCG Gene

Semantic Type

Gene or Genome

UMLS CUI

C1333532

code

C24385