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Chrnetm2Vwi
Targeted Allele Detail
Nomenclature
Symbol: Chrnetm2Vwi
Name: cholinergic receptor, nicotinic, epsilon polypeptide; targeted mutation 2, Veit Witzemann
MGI ID: MGI:5314798
Synonyms: AChRepsilonL221F
Gene: Chrne  Location: Chr11:70614883-70619216 bp, - strand  Genetic Position: Chr11, 43.14 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:182046
Parent Cell Line:  E14.1 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted
Mutation:    Insertion
 
Mutation details
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Chrne Mutation:  4 strains or lines available
References
Original:  J:182046 Chevessier F, et al., A new mouse model for the slow-channel congenital myasthenic syndrome induced by the AChR epsilonL221F mutation. Neurobiol Dis. 2012 Mar;45(3):851-61
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
07/15/2014
MGI 5.18
The Jackson Laboratory