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Slc2a1Rgsc200
Chemically induced Allele Detail
Summary
Symbol: Slc2a1Rgsc200
Name: solute carrier family 2 (facilitated glucose transporter), member 1; RIKEN Genomic Sciences Center (GSC), 200
MGI ID: MGI:3811855
Synonyms: Glut1Rgsc200, M100200
Gene: Slc2a1  Location: Chr4:118965942-118994527 bp, + strand  
Alliance: Slc2a1Rgsc200 page
Mutation
origin
Strain of Origin:  C57BL/6JJcl
Project Collection: RIKEN GSC ENU Project
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThis mutation was identified in an ENU mutagenesis screen, Sequence analysis of the gene revealed a T-to-C mutation in exon 7. This mutation resulted in a substitution of serine with proline at residue 324 of the encoded protein. (J:281292)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Slc2a1 Mutation:  60 strains or lines available
References
Original:  J:133634 RIKEN BioResource Center/RIKEN Genomic Sciences Center, A Large Scale Mutagenesis Program in RIKEN GSC. PhenoSITE, World Wide Web (URL: http://www.brc.riken.jp/lab/gsc/mouse/). 2008;
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
04/23/2024
MGI 6.23
The Jackson Laboratory