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Noa
Gene Detail
 Symbol
Name
ID
Noa
Naruto Otsuka atrichia
MGI:1891009
Feature Type heritable phenotypic marker
Genetic Map
Chromosome Unknown
Mutations,
alleles, and
phenotypes
All mutations/alleles(1) : Spontaneous(1)
 
Heterozygotes for a spontaneous mutation exhibit progressive hair loss and become hairless, ulcerative skin lesions, vibrissae abnormalities, excessive scratching, and increased mast cells and IgE levels.
 
Human Diseases Modeled Using Mouse Noa (1)    Alleles Annotated to Human Diseases(1)   
Other database
links
Entrez Gene170646
References (Earliest) J:43274 Kondo T, et al., The "NOA" MOUSE; A NEW HAIR-DEFICIENT MUTANT (A POSSIBLE ANIMAL MODEL OF ALLERGIC DERMATITIS). Mouse Genome. 1997;95(3):698-700
(Latest) J:208644 Shimizu Y, et al., Potentials of the circulating pruritogenic mediator lysophosphatidic Acid in development of allergic skin inflammation in mice: role of blood cell-associated lysophospholipase d activity of autotaxin. Am J Pathol. 2014 May;184(5):1593-603
All references(7)
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
08/12/2014
MGI 5.19
The Jackson Laboratory