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Fancctm1Mab
Targeted Allele Detail
Nomenclature
Symbol: Fancctm1Mab
Name: Fanconi anemia, complementation group C; targeted mutation 1, Manuel Buchwald
MGI ID: MGI:1858040
Synonyms: Fancc-
Gene: Fancc  Location: Chr13:63304709-63497278 bp, - strand  Genetic Position: Chr13, 32.8 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:32080
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (knock-out)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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 Fancc Mutation:  37 strains or lines available
References
Original:  J:32080 Chen M, et al., Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia. Nat Genet. 1996 Apr;12(4):448-51
All:  29 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
04/15/2014
MGI 5.17
The Jackson Laboratory