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Slc7a11sut
Spontaneous Allele Detail
Nomenclature
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: Chr3:50364936-50499087 bp, - strand  Genetic Position: Chr3, 21.72 cM, cytoband D
Mutation
origin
Strain of Origin:  C3H/HeSnJ
Mutation
description
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
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: 1 anatomical structures
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:  5 strains or lines available
References
Original:  J:14274 Lane PW, Subtle gray (sut); small with kinky tail (skt). Mouse News Lett. 1988;80:165
All:  10 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
08/04/2020
MGI 6.15
The Jackson Laboratory