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KCNJ13
| Symbol: | KCNJ13 | | Name(s): | potassium inwardly-rectifying channel, subfamily J, member 13 | | Type: | protein-coding | | Organism: | Homo sapiens | | Synonyms: | KIR1.4, KIR7.1, MGC33328, SVD | | Links: |
Pubmed,
Entrez Gene,
GeneCards,
BioGPS,
Map Viewer.
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Gene Information from Publications |
| Publication Link |
Summary of findings |
| 18035352 |
This study confirms the expression of Kir7.1 in human RPE, identifies a Kir7.1 splice variant resulting in predicted changes in protein sequence, and indicates that there is no functional interaction between this splice variant and full-length Kir7.1. |
| 18179896 |
These results indicate that the KCNJ13 R162W mutation can cause Snowflake vitreoretinal degeneration and further show that vitreoretinal degeneration can arise through mutations in genes whose products are not structural components of the vitreous. |
Recent Publications on KCNJ13: |  |
Clinical features of the congenital vitreoretinopathies.
The inherited vitreoretinal degenerations or vitreoretinopathies are... | 19th May, 2009
| Department of Ophthalmology, Mayo Clinic, Rochester, MN 55905, USA.
| Eye. 2008 Oct;22(10):1233-42. Epub 2008 Feb 29.
DOI Direct Link |
Evaluation of susceptibility loci in an extended pedigree with idiopathic generalized epilepsy.
PURPOSE: Evaluation of the loci 2q36, 3q26, 5q34 and 14q23 in a German... | 24th June, 2008
| Interdisciplinary Epilepsy-Center, Department of Neurology,
| Epileptic Disord. 2008 Mar;10(1):13-8.
DOI Direct Link |
Expression of Kir7.1 and a novel Kir7.1 splice variant in native human retinal pigment epithelium.
Previous studies on bovine retinal pigment epithelium (RPE) established... | 11th March, 2008
| Department of Ophthalmology and Visual Sciences, University of Michigan,
| Exp Eye Res. 2008 Jan;86(1):81-91. Epub 2007 Oct 2.
DOI Direct Link |
Mutations in KCNJ13 cause autosomal-dominant snowflake vitreoretinal degeneration.
Snowflake vitreoretinal degeneration (SVD, MIM 193230) is a developmental... | 31st January, 2008
| Ophthalmic Genetics and Visual Function Branch, National Eye Institute,
| Am J Hum Genet. 2008 Jan;82(1):174-80.
DOI Direct Link |
Potassium channel gene expression in the rat cochlear nucleus.
Potassium channels play a critical role in defining the... | 4th July, 2007
| Department of Otolaryngology and Communication Sciences, Medical College
| Hear Res. 2007 Jun;228(1-2):31-43. Epub 2007 Jan 31.
DOI Direct Link |
→View more research publications. |
KCNJ13 results (if any) from reagent suppliers | 
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KIR7.1 (C-19) Antibody sc-22440
Species, Gene Name, Gene ID, Chromosome Location, Isoform (mRNA) Accession #, Protein Accession #, OMIM™ Number. Human, KCNJ13, 3769, 2q37.1, NM_002242 ...
http://www.scbt.com/datasheet-22440-kir7-1-c-19-antibody.htm...
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eHandbook 001_050.indd
Kir 7.1 (KCNJ 13). KCNK13 (TALK-2), KCNK15 (TASK-5),. Kv6.1-6.3 (KCNG1-3),. KCNK16 (THIK-2), KCNK17 (THIK-1). Kv8.1(KCNB3), Kv9.1-9.3 (KCNS1-3) ...
http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/RBI_Hand...
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KIR Antibody / KIR Antibodies
製品名, カタログ番号, アイソタイプ, エピトープ, アプリケーション, 動物種. KIR2.1 (N-18) 抗体, sc-18708, goat IgG, N-terminus (h), WB, IP, IF, ELISA, m, r, ...
http://www.scbt.com/ja/table-kir.html...
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Abcam antibodies and reagents product map
... Homeobox protein SIX6 antibodies (1) · IMPDH1 antibodies (1) · IMPG2 antibodies (1) · IQ motif containing B1 antibodies (1) · KCNJ13 antibodies (1)
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http://www.abcam.com/index.html?cl=248&pageconfig=productmap...
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KIR7.1 (C-19) Antibody sc-22440
Species, Nome del gene, Codice del gene, Locus cromosoma, Isoform (mRNA) Accession #, codice accesso proteina, Numero d' ordine. Human, KCNJ13, 3769,
2q37.1 ...
http://www.scbt.com/it/datasheet-22440-kir7-1-c-19-antibody....
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