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Atp2b2Deaf13
Chemically induced Allele Detail
Nomenclature
Symbol: Atp2b2Deaf13
Name: ATPase, Ca++ transporting, plasma membrane 2; deaf 13
MGI ID: MGI:5505458
Synonyms: Deaf13Mrci
Gene: Atp2b2  Location: Chr6:113743842-114042613 bp, - strand  Genetic Position: Chr6, 52.85 cM
Abnormal cochlear hair cells in Atp2b2Deaf11/Atp2b2Deaf11 and Atp2b2Deaf13/Atp2b2Deaf13 mice

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  BALB/c
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a C to A point mutation in exon 9 that results in the amino acid substitution of serine for arginine at position 561 (R561S) in the catalytic core. (J:199859)
Inheritance:    Semidominant
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 Atp2b2 Mutation:  15 strains or lines available
References
Original:  J:199859 Carpinelli MR, et al., Two ENU-induced alleles of Atp2b2 cause deafness in mice. PLoS One. 2013;8(6):e67479
All:  1 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
10/08/2019
MGI 6.14
The Jackson Laboratory