Symbol
Name
ID
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Kcnj10
potassium inwardly-rectifying channel, subfamily J, member 10
MGI:1194504
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Nomenclature History
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STS
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416F4T7
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Synonyms
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BIR10, BIRK-1, Kir1.2, Kir4.1, Kir4.1
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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(3) :
Targeted, knock-out(1)
Targeted, other(1)
Gene trapped(1)
| Homozygous mutant mice show increased input resistance and high depolarization of retinal Muller cells, loss of the endocochlear potential, motor coordination deficits and hindlimb paralysis, and a hypomyelination and spongiform vacuolation in the spinal cord associated with severe axonal pathology. |
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Polymorphisms
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RFLP(2)
SNPs within 2kb(131 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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Expression
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Literature Summary: (4 records)
Data Summary:
Assays (2)
Results (10)
Tissues (6)
Theiler Stages: 13,15,17,25,28
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Assay Type |
Assays |
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Results |
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RT-PCR |
2 |
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10 |
cDNA source data(29)
External Resources:
Allen Brain Atlas
GENSAT
GEO
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Molecular reagents
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All nucleic(40)
Genomic(9)
cDNA(29)
Primer pair(2)
Microarray probesets(2)
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Other database links
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Protein domains
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| InterPro ID |
Description |
| IPR001838 |
Potassium channel, inwardly rectifying, Kir-like |
| IPR003269 |
Potassium channel, inwardly rectifying, Kir1.2 |
| IPR013518 |
Potassium channel, inwardly rectifying, Kir, cytoplasmic |
| IPR013521 |
Potassium channel, inwardly rectifying, Kir, conserved region 2 |
| IPR014756 |
Immunoglobulin E-set |
| IPR016449 |
Potassium channel, inwardly rectifying, Kir |
Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:44256
Tada Y et al.,
"Assignment of the glial inwardly rectifying potassium channel KAB-2/Kir4.1 (Kcnj10) gene to the distal region of mouse chromosome 1."
Genomics 1997 Nov 1;45(3):629-30
(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(27)
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