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Fancgtm1Faw
Targeted Allele Detail
Nomenclature
Symbol: Fancgtm1Faw
Name: Fanconi anemia, complementation group G; targeted mutation 1, Fre Arwert
MGI ID: MGI:2183473
Synonyms: Fancg-
Gene: Fancg  Location: Chr4:43002343-43010506 bp, - strand  Genetic Position: Chr4, 22.97 cM, cytoband B1
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:74737
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA neomycin selection cassette replaced exons 1 through 4. Western blot analysis of splenic lysates and mouse embyronic fibroblasts confirmed the absence of protein in homozygous mutant mice. (J:74737)
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Fancg Mutation:  7 strains or lines available
References
Original:  J:74737 Koomen M, et al., Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice. Hum Mol Genet. 2002 Feb 1;11(3):273-81
All:  8 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/25/2015
MGI 5.21
The Jackson Laboratory