Symbol
Name
ID
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Synonyms
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Myo7, nmf371, USH1B
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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(27)
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Alleles
and
phenotypes
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All alleles(13) :
Spontaneous(4)
Chemically induced(9)
| Homozygotes for spontaneous and chemically induced mutations exhibit deafness, hyperactivity, head-shaking, and circling, with degeneration of the organ of Corti, spiral ganglion, stria vascularis in the cochlea, and vestibular ganglion in the labyrinth. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (8)
Phenotype Images (1)
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Polymorphisms
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RFLP(1)
SNPs within 2kb(469 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
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Expression
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Literature Summary: (47 records)
Data Summary:
Assays (6)
Results (49)
Tissues (19)
Images (30)
Theiler Stages: 19,21,22,23,24,25,26,28
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Assay Type |
Assays |
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Results |
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RNA in situ |
1 |
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7 |
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Immunohistochemistry |
5 |
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42 |
cDNA source data(28)
External Resources:
Allen Brain Atlas
GENSAT
GEO
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Molecular
reagents
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All nucleic(35)
Genomic(6)
cDNA(29)
Antibodies(5)
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:95
Gates WH,
"Linkage of the characters albinism and shaker in the house mouse"
Anat Rec 1929;41():104 (S28 Abstr.)
(Latest)
J:153561
Dominguez-Frutos E et al.,
"Tissue-specific requirements for FGF8 during early inner ear development."
Mech Dev 2009 Oct;126(10):873-81
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All references(137)
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Other
accession IDs
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MGD-MRK-14391, MGD-MRK-14393, MGD-MRK-25940, MGD-MRK-25941, MGI:3587416
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