Symbol
Name
ID
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Synonyms
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BRN-4, Brn4, Otf9
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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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Phenotypes
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All phenotypic
alleles(4) :
Targeted, knock-out(1)
Targeted, other(1)
Spontaneous(1)
Radiation induced(1)
| Homozygotes for spontaneous, radiation-induced and targeted null mutations exhibit developmental malformations of the inner ear resulting in head-shaking and hearing loss. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (4)
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Polymorphisms
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All PCR and RFLP(3) :
PCR(1)
RFLP(2)
SNPs within 2kb(2 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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All GO classifications(15)
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Expression
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Literature Summary: (34 records)
Data Summary:
Assays (8)
Results (212)
Tissues (137)
Images (17)
Theiler Stages: 13,17,19,20,21,22,23,25,28
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Assay Type |
Assays |
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Results |
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RNA in situ |
6 |
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206 |
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Immunohistochemistry |
2 |
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6 |
cDNA source data(5)
External Resources:
GENSAT
GEO
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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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Molecular reagents
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All nucleic(14)
Genomic(3)
cDNA(7)
Primer pair(2)
Other(2)
Antibodies(1)
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References
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(Earliest)
J:13741
Phillips RJS et al.,
"New sex-linked mutant - Bhd"
Mouse News Lett 1978;58():43-4
(Latest)
J:134489
Trowe MO et al.,
"Deafness in mice lacking the T-box transcription factor Tbx18 in otic fibrocytes."
Development 2008 May;135(9):1725-34
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All references(56)
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Other accession IDs
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MGD-MRK-13084, MGD-MRK-14438, MGD-MRK-1626, MGD-MRK-18721, MGI:98317
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