Symbol
Name
ID
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Synonyms
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Gm9815, nmf19, Ush1f
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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(24)
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Alleles
and
phenotypes
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All alleles(11) :
Gene trapped(2)
Transgenic(1)
Spontaneous(6)
Chemically induced(2)
| Homozygotes for severe mutations exhibit circling, head-tossing, hyperactivity, impaired swimming and profound deafness. Mice have defects in cochlea and degeneration of hair cells, spiral ganglion cells and saccular macula. Females are poor mothers. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (2)
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Polymorphisms
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RFLP(1)
SNPs within 2kb(4716 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
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Expression
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Literature Summary: (2 records)
Data Summary:
Assays (1)
Results (40)
Tissues (38)
Images (16)
Theiler Stages: 20,22,24,28
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Assay Type |
Assays |
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Results |
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RNA in situ |
1 |
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40 |
cDNA source data(24)
External Resources:
Allen Brain Atlas
GEO
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Molecular
reagents
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All nucleic(26)
Genomic(1)
cDNA(25)
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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:14990
Schaible RH,
"av"
Mouse News Lett 1957;15():29
(Latest)
J:151359
Lelli A et al.,
"Tonotopic gradient in the developmental acquisition of sensory transduction in outer hair cells of the mouse cochlea."
J Neurophysiol 2009 Jun;101(6):2961-73
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All references(40)
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Other
accession IDs
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MGD-MRK-1480, MGI:2143894, MGI:2183461, MGI:3710651, MGI:88118
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