gnd
Gene Detail

Symbol Name ID

gnd generalized neuroaxonal dystrophy MGI:95786

Feature Type

heritable phenotypic marker

Genetic Map

Chromosome Unknown

Alleles and phenotypes

All 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 Gene

14698

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)

Other accession IDs

MGD-MRK-10205