Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Cochtm1.1Stw
Name:	cochlin; targeted mutation 1.1, Colin L Stewart
MGI ID:	MGI:3624560
Synonyms:	Coch-
Gene:	Coch  Location: Chr12:51640156-51652558 bp, + strand  Genetic Position: Chr12, 22.11 cM
Alliance:	Cochtm1.1Stw page

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+

Allele Type:    Targeted (Null/knockout) Mutation:    Intragenic deletion   Mutation details: Exons 7-11 and part of exon 12, encoding the two vWA domains and remaining cochlin protein downstream of the LCCL domain, were removed via cre mediated recombination. Neither full length or truncated transcripts were detected in mutants. (J:105566)

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:	2 assay results
In Structures Affected by this Mutation:	1 anatomical structure(s)

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:	42 strains or lines available

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:	9 reference(s)