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Abcc9tm1Cfb
Targeted Allele Detail
Nomenclature
Symbol: Abcc9tm1Cfb
Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 9; targeted mutation 1, Charles F Burant
MGI ID: MGI:2155916
Synonyms: Sur2 -
Gene: Abcc9  Location: Chr6:142587862-142702274 bp, - strand  Genetic Position: Chr6, 74.35 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:71840
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Duplication, Insertion, Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Abcc9 Mutation:  4 strains or lines available
Notes
Phenotypic Similarity to Human Syndrome: Prinzmetal or variant angina (J:78066)

References
Original:  J:71840 Chutkow WA, et al., Disruption of Sur2-containing KATP channels enhances insulin-stimulated glucose uptake in skeletal muscle. Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11760-4
All:  10 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
12/09/2014
MGI 5.20
The Jackson Laboratory