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Rs1tmgc1
Chemically induced Allele Detail
Summary
Symbol: Rs1tmgc1
Name: retinoschisis (X-linked, juvenile) 1 (human); Tennessee Mouse Genome Consortium 1
MGI ID: MGI:2448640
Synonyms: 44TNJ
Gene: Rs1  Location: ChrX:159551009-159582659 bp, + strand  Genetic Position: ChrX, 73.95 cM
Alliance: Rs1tmgc1 page
Mutation
origin
Strain of Origin:  C57BL/6JRn
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThis phenotypic mutant was identified in an ENU mutagenesis screen. A C to T transition at the second base of intron 2 led to two novel splice variants. One mutant transcript contains a 10 bp deletion while the other has a 26 bp deletion, both leading to a frameshift mutation. (J:99982)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 10 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 Rs1 Mutation:  6 strains or lines available
References
Original:  J:81149 The Tennessee Mouse Genome Consortium, Targeted mutagenesis of the mouse genome and neural phenotypes. MGI Direct Data Submission. 2003;
All:  5 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
04/16/2024
MGI 6.23
The Jackson Laboratory