Symbol
Name
ID
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Synonyms
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9630007J19Rik, Dbv, flail, MVa, Myo5, MyoVA, nmf244
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Genetic Map
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Sequence Map
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Mammalian
homology
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Sequences
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All sequences(21)
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Alleles
and
phenotypes
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All alleles(72) :
Targeted, other(1)
Gene trapped(2)
Spontaneous(52)
Chemically induced(17)
| Mutations in this gene cause abnormal melanocyte structure, resulting in clumping of melanin pigment in hair of nonagouti mice, producing a gray coat color. Some alleles also produce a lethal or neurological phenotype. Normal melanocyte structure and coat phenotype is restored in revertant alleles. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (1)
Phenotype Images (4)
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Polymorphisms
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RFLP(17)
SNPs within 2kb(419 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
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Expression
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Literature Summary: (3 records)
cDNA source data(17)
External Resources:
Allen Brain Atlas
GEO
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Molecular
reagents
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All nucleic(42)
Genomic(19)
cDNA(21)
Other(2)
Microarray probesets(2)
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Other database
links
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Protein
domains
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Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:28864
Gates WH,
"Linkage of Short Ear and Density in the House Mouse."
Proc Natl Acad Sci U S A 1927 Aug;13(8):575-8
(Latest)
J:148845
Alami NH et al.,
"Myosin Va increases the efficiency of neurofilament transport by decreasing the duration of long-term pauses."
J Neurosci 2009 May 20;29(20):6625-34
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All references(221)
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Other
accession IDs
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MGD-MRK-14365, MGD-MRK-2338, MGD-MRK-28030, MGD-MRK-33656, MGD-MRK-8805, MGI:1096356, MGI:1343057, MGI:2143030, MGI:2143108
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