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Sox10tm1Weg
Targeted Allele Detail
Summary
Symbol: Sox10tm1Weg
Name: SRY (sex determining region Y)-box 10; targeted mutation 1, Michael Wegner
MGI ID: MGI:2151173
Synonyms: Sox10-, Sox10lacZ, Sox10LacZKO
Gene: Sox10  Location: Chr15:79039113-79048690 bp, - strand  Genetic Position: Chr15, 37.7 cM
Alliance: Sox10tm1Weg page
Lack of pigmentation and megacolon in Sox10gt/Sox10tm1Weg pups

Show the 4 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:67383
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsIn-frame insertion of a lacZ-neomycin resistance cassette replaced the coding sequences. RT-PCR studies did not detect wild-type transcript in homozygous E12.5 embryos. (J:67383)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 905 assay results
In Structures Affected by this Mutation: 13 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Sox10 Mutation:  33 strains or lines available
References
Original:  J:67383 Britsch S, et al., The transcription factor Sox10 is a key regulator of peripheral glial development. Genes Dev. 2001 Jan 1;15(1):66-78
All:  61 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
11/19/2024
MGI 6.24
The Jackson Laboratory