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Agtpbp1pcd
Spontaneous Allele Detail
Nomenclature
Symbol: Agtpbp1pcd
Name: ATP/GTP binding protein 1; Purkinje cell degeneration
MGI ID: MGI:1856535
Synonyms: Nna1pcd, pcd, pcd1J
Gene: Agtpbp1  Location: Chr13:59449537-59585227 bp, - strand  Genetic Position: Chr13, 31.87 cM
Agtpbp1pcd/Agtpbp1pcd mouse

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

Mutation
origin
Strain of Origin:  C57BR/cdJ
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Undefined
 
Mutation detailsNo overt mutations were noted in the coding region for this allele. Northern analysis failed to detect transcript in all tissues except for testis, where reduced levels were noted. Authors note that the mutation is likely in a regulatory region of the gene. (J:74929)
Inheritance:    Recessive
Phenotypes
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Disease models
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Expression
In Mice Carrying this Mutation: 1 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Agtpbp1 Mutation:  12 strains or lines available
References
Original:  J:5613 Mullen RJ, et al., Purkinje cell degeneration, a new neurological mutation in the mouse. Proc Natl Acad Sci U S A. 1976 Jan;73(1):208-12
All:  90 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
01/20/2015
MGI 5.21
The Jackson Laboratory