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Mesdmesd
Radiation induced Allele Detail
Summary
Symbol: Mesdmesd
Name: mesoderm development LRP chaperone; mesoderm development
MGI ID: MGI:1856955
Synonyms: implantation survival, IS, msd
Gene: Mesd  Location: Chr7:83533074-83549519 bp, + strand  Genetic Position: Chr7, 48.35 cM
Alliance: Mesdmesd page
Mutation
origin
Strain of Origin:  (C3H/Rl x 101/Rl)F1
Mutation
description
Allele Type:    Radiation induced
Inheritance:    Recessive
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 Mesd Mutation:  15 strains or lines available
Notes
Embryos homozygous for radiation induced deletions in the region of the tyrosinase locus (Tyr) which encompass the mesd locus are completely devoid of mesoderm, and begin to degenerate at about 11 days of gestation. Embryonic and extraembryonic ectoderms are present. mesd is the most proximal locus affected by Tyr deletions (J:1540).
References
Original:  J:1540 Klebig ML, et al., Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development. Mamm Genome. 1992;2(1):51-63
All:  3 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
03/18/2025
MGI 6.24
The Jackson Laboratory