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Rps7Mtu
Chemically induced Allele Detail
Summary
Symbol: Rps7Mtu
Name: ribosomal protein S7; montu
MGI ID: MGI:3043039
Synonyms: BHV19
Gene: Rps7  Location: Chr12:28680853-28685952 bp, - strand  Genetic Position: Chr12, 10.99 cM, cytoband C1
Alliance: Rps7Mtu page
Rps7Mtu/Rps7+ mice exhibiting a white belly spot and kinked tail

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  BALB/cOlaHsd
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to G transversion (c.574>G) that results in the amino acid substitution of glycine for valine at position 156 (V156G). (J:195156)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Rps7 Mutation:  16 strains or lines available
References
Original:  J:93195 Bogani D, et al., New semidominant mutations that affect mouse development. Genesis. 2004 Oct;40(2):109
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
12/10/2024
MGI 6.24
The Jackson Laboratory