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Ostm1gl
Spontaneous Allele Detail
Nomenclature
Symbol: Ostm1gl
Name: osteopetrosis associated transmembrane protein 1; grey-lethal
MGI ID: MGI:1856885
Synonyms: gl, grey lethal
Gene: Ostm1  Location: Chr10:42583822-42702459 bp, + strand  Genetic Position: Chr10, 22.89 cM
Ostm1gl/Ostm1gl and control

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

Mutation
origin
Strain of Origin:  STOCK Tyrc-e
Mutation
description
Allele Type:    Spontaneous
Mutations:    Intragenic deletion, Transposon insertion
 
Mutation detailsThe mutation in the grey lethal mouse was identified as a genomic deletion of the 5' region of the gene. The deletion spanned 7.5 kb and included the promoter, the first exon and part of the first intron. The genomic sequence also included 460 bp corresponding to the 3' UTR of a LINE1 element at the deletion breakpoints. (J:82658)
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 12 assay results
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 Ostm1 Mutation:  7 strains or lines available
References
Original:  J:15551 Gruneberg H, A new sub-lethal colour mutation in the house mouse. Proc R Soc Lond B Biol Sci. 1935;118:321-42
All:  21 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
01/20/2015
MGI 5.21
The Jackson Laboratory