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Slc45a2uw-7J
Spontaneous Allele Detail
Summary
Symbol: Slc45a2uw-7J
Name: solute carrier family 45, member 2; underwhite 7 Jackson
MGI ID: MGI:5448551
Gene: Slc45a2  Location: Chr15:11000807-11029319 bp, + strand  Genetic Position: Chr15, 5.4 cM
Alliance: Slc45a2uw-7J page
Mutation
origin
Strain of Origin:  C3H/HeJ-Mfs/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA spontaneous T-to-G point mutation in chromosome 15 position 11023400 (GRCm38), causes tyrosine codon 363 to change to a premature stop codon (p.Y363*). (J:190733)
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: 2 anatomical structure(s)
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 Slc45a2 Mutation:  55 strains or lines available
References
Original:  J:190733 Karst SY, et al., Underwhite 7 Jackson, a spontaneous point mutation in Slc45a2. MGI Direct Data Submission. 2013;
All:  1 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
11/12/2024
MGI 6.24
The Jackson Laboratory