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inad
Gene Detail
Symbol

Name
ID
inad
infantile neuroaxonal dystrophy
MGI:3577064
Feature Type
heritable phenotypic marker
Genetic Map
Chromosome 1
Syntenic

Mapping data(1)
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Spontaneous(1)
 
Homozygous mutant mice die before sexual maturity and exhibit axonal dystrophic change appearing as spheroid bodies in the nervous system. Mice show progressive motor paralysis and atrophy of the hindlimbs.
 
Human Diseases Modeled Using Mouse inad (1)    Alleles Annotated to Human Diseases(1)    Phenotype Images(2)
References
(Earliest) J:97670 Matsushima Y, et al., A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1. Mamm Genome. 2005 Feb;16(2):73-8
All references(1)
Disease annotation references (1)

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
12/09/2014
MGI 5.20
The Jackson Laboratory