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Gene : FANCG Homo sapiens

Name  ? FA complementation group G Cytological Location  9p13.3
Brief Description  FA complementation group G
Description  The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G. [provided by RefSeq, Jul 2008]
  • synonyms:
  • HGNC:3588,
  • DNA repair protein XRCC9,
  • NM_004629,
  • OTTHUMG00000019850,
  • AJ007669,
  • XRCC9,
  • X-ray repair, complementing defective, in Chinese hamster, 9,
  • XRCC9,
  • Fanconi anemia complementation group G,
  • FAG,
  • uc003zwb.1,
  • X-ray repair complementing defective repair in Chinese hamster cells 9,
  • FAG,
  • identifiers:
  • 2189,
  • ENSG00000221829,

Genome feature

Region: gene ? Length: 6104  
Location: 9:35073839-35079942 reverse strand Cyto location: 9p13.3

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3753 SN Ps

5 Cross References

17 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results