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Trak1hyrt
Spontaneous Allele Detail
Nomenclature
Symbol: Trak1hyrt
Name: trafficking protein, kinesin binding 1; hypertonic
MGI ID: MGI:3044768
Synonyms: hyrt, nm1952
Gene: Trak1  Location: Chr9:121297502-121474918 bp, + strand  Genetic Position: Chr9, 72.41 cM
Mutation
origin
Strain of Origin:  AKR
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThere is a 20 bp deletion in the last exon of the gene. This results in a frame shift after the codon for amino acid 824. 12% of the protein is disrupted. (J:90779, J:105231)
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 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 Trak1 Mutation:  2 strains or lines available
References
Original:  J:90779 Gilbert SL, et al., Characterization of the hypertonic mutant mouse. MGI Direct Data Submission. 2004;
All:  2 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
07/31/2018
MGI 6.12
The Jackson Laboratory