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Cox15m1Mhda
Chemically induced Allele Detail
Summary
Symbol: Cox15m1Mhda
Name: cytochrome c oxidase assembly protein 15; mutation 1, Martin Hrabe de Angelis
MGI ID: MGI:5707593
Synonyms: Cox-01, Cox15V187F, Cox15V187FMhda
Gene: Cox15  Location: Chr19:43721693-43741439 bp, - strand  Genetic Position: Chr19, 36.67 cM
Alliance: Cox15m1Mhda page
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsThe mutation comprises a G-to-T transversion at nucleotide position 559, resulting in replacement of valine by phenylalanine at amino acid position 187 of the protein (V187F). (J:82809)
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Cox15 Mutation:  26 strains or lines available
References
Original:  J:82809 European Mouse Mutant Archive, Information obtained from the European Mouse Mutant Archive (EMMA). Unpublished. 2003-2013;
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
04/16/2024
MGI 6.23
The Jackson Laboratory