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Spontaneous Allele Detail
Symbol: Slc7a11sut
Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 11; subtle gray
MGI ID: MGI:1857061
Synonyms: sut
Gene: Slc7a11  Location: Chr3:50319385-50403947 bp, - strand  Genetic Position: Chr3, 21.72 cM, cytoband D
Alliance: Slc7a11sut page
Strain of Origin:  C3H/HeSnJ
Allele Type:    Spontaneous
Mutations:    Insertion, Intragenic deletion
Mutation detailsSequencing revealed a large deletion extending from intron 11 through exon 12 and into the intergenic region, creating a new splice site and the replacement of exon 12 with exon 12'. 3' RACE revealed a new stop codon in exon 12' and predicted a modified and truncated protein carboxyl terminus. (J:100476)
Inheritance:    Recessive
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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 Slc7a11 Mutation:  49 strains or lines available
Original:  J:14274 Lane PW, Subtle gray (sut); small with kinky tail (skt). Mouse News Lett. 1988;80:165
All:  12 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
MGI 6.23
The Jackson Laboratory