FANCG

GENE INFORMATION

? »

Gene name

FANCG (HGNC Symbol)

Synonyms

FAG, XRCC9

Description

Fanconi anemia, complementation group G (HGNC Symbol)

Entrez gene summary

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]

Chromosome

9 (Chromosome progress)

Cytoband

p13.3

Chromosome location (bp)

35073832 - 35080013

Ensembl

ENSG00000221829 (version 73.37)

Entrez gene

2189

UniProt

O15287 (UniProt - Evidence at protein level)

neXtProt

NX_O15287

Antibodypedia

FANCG antibodies
 

PROTEIN VIEW

? »
 
 
 
FANCG-001
 
FANCG-003
 
FANCG-005
 
 
 
 
 

PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

FANCG-001 ENSP00000367910
ENST00000378643
O15287
Show all »
Show » Show » 622 68.6 No 0
FANCG-003 ENSP00000409607
ENST00000448890
C9JSE3
Show all »
Show » Show » 215 23.7 No 0
FANCG-005 ENSP00000412793
ENST00000425676
F8WC08
Show all »
Show » 106 11.8 No 0