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Mesdtm1Bch
Targeted Allele Detail
Summary
Symbol: Mesdtm1Bch
Name: mesoderm development LRP chaperone; targeted mutation 1, Bernadette C Holdener
MGI ID: MGI:4939501
Synonyms: Mesdc2tm1Bch, Mesdtm1bch
Gene: Mesd  Location: Chr7:83533074-83549519 bp, + strand  Genetic Position: Chr7, 48.35 cM
Alliance: Mesdtm1Bch page
The Mesdtm2.1Bch allele does not complement the Mesdtm1Bch and Tyrc-3YPSd alleles

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:168622
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    Exon 2 and 3 were replaced with a neo cassette. (J:168622)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 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 Mesd Mutation:  15 strains or lines available
References
Original:  J:168622 Lighthouse JK, et al., MESD is essential for apical localization of megalin/LRP2 in the visceral endoderm. Dev Dyn. 2011 Mar;240(3):577-88
All:  2 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
12/17/2024
MGI 6.24
The Jackson Laboratory