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Atp2b2dfw
Spontaneous Allele Detail
Summary
Symbol: Atp2b2dfw
Name: ATPase, Ca++ transporting, plasma membrane 2; deaf waddler
MGI ID: MGI:1856799
Synonyms: deafwaddler, dfw
Gene: Atp2b2  Location: Chr6:113720803-114019574 bp, - strand  Genetic Position: Chr6, 52.85 cM
Alliance: Atp2b2dfw page
Mutation
origin
Strain of Origin:  C3H/HeJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA G to A transition point mutation at position 847 is predicted to cause a glycine to serine substitution at position 283 in the encoded protein. (J:48969)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
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 Atp2b2 Mutation:  66 strains or lines available
References
Original:  J:14114 Lane PW, Deaf waddler (dfw). Mouse News Lett. 1987;77:129
All:  10 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
12/10/2024
MGI 6.24
The Jackson Laboratory