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Fancatm1Faw
Targeted Allele Detail
Summary
Symbol: Fancatm1Faw
Name: Fanconi anemia, complementation group A; targeted mutation 1, Fre Arwert
MGI ID: MGI:2183470
Synonyms: Fanca-
Gene: Fanca  Location: Chr8:123995039-124045315 bp, - strand  Genetic Position: Chr8, 72.1 cM
Alliance: Fancatm1Faw page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:63742
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExons 4 through 7 were deleted by the insertion of a cassette comprised of a splice acceptor site, IRES-lacZ, and neo. Protein was undetected in homozygous mutant mice via Western blot analysis of splenic tissue. (J:63742)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 6 anatomical structure(s)
Tumor Data
List all tumor models in MMHCdb carrying Fancatm1Faw
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 Fanca Mutation:  81 strains or lines available
References
Original:  J:63742 Cheng NC, et al., Mice with a targeted disruption of the fanconi anemia homolog fanca. Hum Mol Genet. 2000 Jul 22;9(12):1805-11
All:  20 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory