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Cochtm1.1Stw
Targeted Allele Detail
Nomenclature
Symbol: Cochtm1.1Stw
Name: coagulation factor C homolog (Limulus polyphemus); targeted mutation 1.1, Colin L Stewart
MGI ID: MGI:3624560
Synonyms: Coch-
Gene: Coch  Location: Chr12:51593341-51605773 bp, + strand  Genetic Position: Chr12, 22.11 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:105566
Parent Cell Line:  W9.5/W95 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 2 assay results
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 Coch Mutation:  7 strains or lines available
References
Original:  J:105566 Rodriguez CI, et al., Cochlin, a secreted von Willebrand factor type a domain-containing factor, is regulated by leukemia inhibitory factor in the uterus at the time of embryo implantation. Endocrinology. 2004 Mar;145(3):1410-8
All:  5 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
09/09/2014
MGI 5.19
The Jackson Laboratory