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Rps7Zma
Chemically induced Allele Detail
Summary
Symbol: Rps7Zma
Name: ribosomal protein S7; zuma
MGI ID: MGI:5500069
Gene: Rps7  Location: Chr12:28680853-28685952 bp, - strand  Genetic Position: Chr12, 10.99 cM, cytoband C1
Alliance: Rps7Zma page
Skeletal abnormalities in Rps7Zma/Rps7+ mutants

Show the 9 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  BALB/c
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU-mutagenesis induced an A to C transversion in exon 7 (c.637A>C) resulted in the amino acid substitution of a serine for tyrosine at position 177 (Y177S). (J:195156)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 12 anatomical structure(s)
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 Rps7 Mutation:  16 strains or lines available
References
Original:  J:195156 Watkins-Chow DE, et al., Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes. PLoS Genet. 2013 Jan;9(1):e1003094
All:  1 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
06/12/2024
MGI 6.13
The Jackson Laboratory