FANCG Gene
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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
Contributing Source
CTRP
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