Symbol
Name
ID
|
|
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Genetic Map
|
|
Chromosome 16
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cytoband C3-4
|
|
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Mapping data(
4)
|
|
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Sequence Map
|
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Mammalian
homology
|
|
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Sequences
|
All sequences(24)
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Alleles
and
phenotypes
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All alleles(50) :
Targeted, other(1)
Gene trapped(49)
| Homozygous mutant mice have a normal endocochlear potential but are deaf due to cochlear hair cell degeneration within the first 3 weeks of age. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (1)
|
|
Polymorphisms
|
SNPs within 2kb(630 from dbSNP Build 128)
|
Gene Ontology
(GO)
classifications
|
|
|
Expression
|
Literature Summary: (2 records)
Data Summary:
Assays (4)
Results (67)
Tissues (65)
Images (3)
Theiler Stages: 13,15,17,20,22,23,26,28
| |
Assay Type |
Assays |
|
Results |
| |
RT-PCR |
2 |
|
18 |
| |
RNA in situ |
2 |
|
49 |
cDNA source data(6)
External Resources:
Allen Brain Atlas
GEO
|
Molecular
reagents
|
All nucleic(10)
Genomic(2)
cDNA(6)
Primer pair(2)
Microarray probesets(2)
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Other database
links
|
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Protein
domains
|
Graphical View
of Protein Domain Structure
|
|
References
|
(Earliest)
J:64941
Morita K et al.,
"Claudin-11/OSP-based tight junctions of myelin sheaths in brain and Sertoli cells in testis."
J Cell Biol 1999 May 3;145(3):579-88
(Latest)
J:86696
Zambrowicz BP et al.,
"Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention."
Proc Natl Acad Sci U S A 2003 Nov 25;100(24):14109-14
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All references(10)
|
Other
accession IDs
|
MGI:2146507
|
