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Oxtrtm1.2Wsy
Targeted Allele Detail
Summary
Symbol: Oxtrtm1.2Wsy
Name: oxytocin receptor; targeted mutation 1.2, W Scott Young III
MGI ID: MGI:3800792
Gene: Oxtr  Location: Chr6:112450644-112466904 bp, - strand  Genetic Position: Chr6, 52.27 cM, cytoband E3
Alliance: Oxtrtm1.2Wsy page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:137445
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsExons 2 and 3 were removed by germ line, cre-mediated recombination. The absence of protein expression was confirmed by autoradiolabeling with 125-Iodine ornithine vasotocin, an Otx anatagonist. (J:137445)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Oxtr Mutation:  40 strains or lines available
References
Original:  J:137445 Lee HJ, et al., A conditional knockout mouse line of the oxytocin receptor. Endocrinology. 2008 Jul;149(7):3256-63
All:  5 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