About   Help   FAQ
Lama2tm1Eeng
Targeted Allele Detail
Nomenclature
Symbol: Lama2tm1Eeng
Name: laminin, alpha 2; targeted mutation 1, Eva Engvall
MGI ID: MGI:3522319
Synonyms: dyw, Lama2dy-W
Gene: Lama2  Location: Chr10:26981288-27616942 bp, - strand  Genetic Position: Chr10, 14.23 cM, cytoband A4-B1
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:49435
Parent Cell Line:  CJ7 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Targeted (Reporter)
Mutation:    Insertion
 
Mutation details
Phenotypes
Loading...
View phenotypes for all genotypes (concatenated display).
Disease models
Loading...
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 Lama2 Mutation:  7 strains or lines available
References
Original:  J:49435 Kuang W, et al., Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models. J Clin Invest. 1998 Aug 15;102(4):844-52
All:  21 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/08/2014
MGI 5.17
The Jackson Laboratory