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Fhittm1Hbn
Targeted Allele Detail
Nomenclature
Symbol: Fhittm1Hbn
Name: fragile histidine triad gene; targeted mutation 1, Kay Huebner
MGI ID: MGI:2176611
Synonyms: Fhit-, Fhittm2KCC
Gene: Fhit  Location: Chr14:9550092-11162035 bp, - strand  Genetic Position: Chr14, 5.61 cM, cytoband A2
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:61946
Parent Cell Line:  RW-4 (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutation:    Insertion
 
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 Fhit Mutation:  3 strains or lines available
References
Original:  J:61946 Fong LY, et al., Muir-torre-like syndrome in fhit-deficient mice. Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4742-7
All:  14 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
09/09/2014
MGI 5.19
The Jackson Laboratory