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Procrtm2Cte
Targeted Allele Detail
Summary
Symbol: Procrtm2Cte
Name: protein C receptor, endothelial; targeted mutation 2, Charles T Esmon
MGI ID: MGI:3702857
Synonyms: EPCRflox, ProcrLox
Gene: Procr  Location: Chr2:155593037-155597391 bp, + strand  Genetic Position: Chr2, 77.26 cM, cytoband H1-3
Alliance: Procrtm2Cte page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:80043
Parent Cell Line:  Other (see notes) (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1b-m2
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsThis allele is the parent allele of Procrtm1Cte, whereby exon 1 was flanked by loxP sites with a neomycin resistance cassette and a third loxP site in intron 2. (J:80043)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
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 Procr Mutation:  15 strains or lines available
Notes
ES cell line = AB2.
References
Original:  J:80043 Gu JM, et al., Disruption of the endothelial cell protein C receptor gene in mice causes placental thrombosis and early embryonic lethality. J Biol Chem. 2002 Nov 8;277(45):43335-43
All:  8 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory