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Abcg5trac
Spontaneous Allele Detail
Nomenclature
Symbol: Abcg5trac
Name: ATP-binding cassette, sub-family G (WHITE), member 5; thrombocytopenia and cardiomyopathy
MGI ID: MGI:2156990
Synonyms: cardiomyopathy, cmp, tac
Gene: Abcg5  Location: Chr17:84658234-84683011 bp, - strand  Genetic Position: Chr17, 55.02 cM
Mutation
origin
Strain of Origin:  A/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
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: 2 strains available      Cell Lines: 0 lines available
Carrying any Abcg5 Mutation:  6 strains or lines available
References
Original:  J:157223 Chase TH, et al., The mouse mutation 'thrombocytopenia and cardiomyopathy' (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia. Blood. 2010 Feb 11;115(6):1267-76
All:  1 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
11/18/2014
MGI 5.20
The Jackson Laboratory