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Ocmtm1.1Ddsi
Targeted Allele Detail
Nomenclature
Symbol: Ocmtm1.1Ddsi
Name: oncomodulin; targeted mutation 1.1, Dwayne Simmons
MGI ID: MGI:4366443
Gene: Ocm  Location: Chr5:144019804-144026670 bp, - strand  Genetic Position: Chr5, 82.85 cM, cytoband G1-3
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:231626
Parent Cell Line:  SCC10 (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThis allele was generated by crossing a Ocmtm1Ddsi homozygous mouse with a mouse expressing Cre recombinase ubiquitously from a beta-actin promoter. Exons two through four have been deleted from the endogenous gene. (J:231626)
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 Ocm Mutation:  8 strains or lines available
References
Original:  J:231626 Tong B, et al., Oncomodulin, an EF-Hand Ca2+ Buffer, Is Critical for Maintaining Cochlear Function in Mice. J Neurosci. 2016 Feb 3;36(5):1631-5
All:  2 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
03/31/2020
MGI 6.15
The Jackson Laboratory