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gnd
Gene Detail
 Symbol
Name
ID
gnd
generalized neuroaxonal dystrophy
MGI:95786
Feature Type heritable phenotypic marker
Genetic Map
Chromosome Unknown
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Spontaneous(1)
 
Mice homozygous for a spontaneous mutation breed only rarely, display a dull hair coat and small body size, and progressively develop a hunched posture, shaky gait and hindlimb paralysis associated with generalized neuroaxonal dystrophy.
 
Human Diseases Modeled Using Mouse gnd (1)    Alleles Annotated to Human Diseases(1)   
Gene Ontology
(GO)
classifications
All GO classifications: (7 annotations)
Process adult behavior, adult locomotory behavior, ...
Other database
links
Entrez Gene14698
References (Earliest) 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 references(2)
Disease annotation references (1)
Other
accession IDs
MGD-MRK-10205

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
09/23/2014
MGI 5.19
The Jackson Laboratory