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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: Chr3:50364936-50443613 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 details
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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
Notes
Phenotypic Similarity to Human Syndrome: Hermansky-Pudlak Syndrome (J:31616)

References
Original:  J:14274 Lane PW, Subtle gray (sut); small with kinky tail (skt). Mouse News Lett. 1988;80:165
All:  8 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/26/2014
MGI 5.19
The Jackson Laboratory