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M412b
Chemically induced Allele Detail
Summary
Symbol: M412b
Name: mutant 412b
MGI ID: MGI:5515447
Synonyms: line 412
Gene: M412b  Location: unknown  Genetic Position: Chr13, Syntenic
Alliance: M412b page
Mutation
origin
Strain of Origin:  mixed
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Undefined
 
Mutation detailsThis mutation was identified in an ENU mutagenesis screen focused on the Del(13)36H deletion interval. (J:101156)
Phenotypes
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View phenotypes and curated references 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: 2 strains available      Cell Lines: 0 lines available
Carrying any M412b Mutation:  2 strains or lines available
Notes
This allele was induced by ENU treatment of a male mouse homozygous for Foxq1sa on a mixed genetic background (mostly 101 and C3H, but derived from a linkage testing stock also homozygous for Wnt3avt (origin: C57BR) and Bloc1s5mu (origin: t-allele stock)).
References
Original:  J:101156 Bogani D, et al., Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12477-82
All:  1 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