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Symbol Name ID |
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| Feature Type | heritable phenotypic marker | ||
| Genetic Map |
Chromosome Unknown
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Alleles and phenotypes |
All 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) |
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Other database links |
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| 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:105469 Kondo T, et al., Development of Dry Skin in the NOA Mouse Under Individual Housing Conditions: A Potentially Useful Animal Model for Evaluating Moisturizing Effects. Exp Anim. 2005 Oct;54(5):429-36 All references(6) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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