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Atp8a2wl-vmd
Spontaneous Allele Detail
Nomenclature
Symbol: Atp8a2wl-vmd
Name: ATPase, aminophospholipid transporter-like, class I, type 8A, member 2; wabbler lethal vestibulomotor degeneration
MGI ID: MGI:1856273
Synonyms: vmd
Gene: Atp8a2  Location: Chr14:59647531-60086914 bp, - strand  Genetic Position: Chr14, 31.49 cM
Mutation
origin
Strain of Origin:  C3H/HeSnJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsA 9167 bp deletion removes exon 32. This results in a 32 amino acid deletion in the ninth transmembrane domain. (J:188127, J:222308)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 2 anatomical structures
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 Atp8a2 Mutation:  9 strains or lines available
References
Original:  J:11718 Bronson RT, et al., Genetic and age related models of neurodegeneration in mice: dystrophic axons. J Neurogenet. 1992 May;8(2):71-83
All:  6 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
02/18/2020
MGI 6.14
The Jackson Laboratory