Homo sapiens Gene: KCNJ13 | |||||||||||
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Summary | |||||||||||
InnateDB Gene | IDBG-83393.6 | ||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||
Gene Symbol | KCNJ13 | ||||||||||
Gene Name | potassium inwardly-rectifying channel, subfamily J, member 13 | ||||||||||
Synonyms | KIR1.4; KIR7.1; LCA16; SVD | ||||||||||
Species | Homo sapiens | ||||||||||
Ensembl Gene | ENSG00000115474 | ||||||||||
Encoded Proteins |
potassium inwardly-rectifying channel, subfamily J, member 13
potassium inwardly-rectifying channel, subfamily J, member 13
potassium inwardly-rectifying channel, subfamily J, member 13
potassium inwardly-rectifying channel, subfamily J, member 13
potassium inwardly-rectifying channel, subfamily J, member 13
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Protein Structure | |||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||
Entrez Gene | |||||||||||
Summary |
This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010] |
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Gene Information | |||||||||||
Type | Protein coding | ||||||||||
Genomic Location | Chromosome 2:232766464-232776568 | ||||||||||
Strand | Reverse strand | ||||||||||
Band | q37.1 | ||||||||||
Transcripts |
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Interactions | |||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Pathways | |||||||||||
NETPATH | |||||||||||
REACTOME | |||||||||||
KEGG |
Protein digestion and absorption pathway
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INOH | |||||||||||
PID NCI | |||||||||||
Cross-References | |||||||||||
SwissProt | O60928 | ||||||||||
TrEMBL | C9JWD6 | ||||||||||
UniProt Splice Variant | |||||||||||
Entrez Gene | 3769 | ||||||||||
UniGene | Hs.467338 Hs.661477 | ||||||||||
RefSeq | NM_001172416 NM_002242 | ||||||||||
HUGO | HGNC:6259 | ||||||||||
OMIM | 603208 | ||||||||||
CCDS | CCDS2498 CCDS54437 | ||||||||||
HPRD | |||||||||||
IMGT | |||||||||||
EMBL | AB013889 AB013891 AC064852 AF061118 AF082182 AJ006128 AJ007557 AK314019 AY758240 AY758241 BC037290 CH471063 | ||||||||||
GenPept | AAC15769 AAD08673 AAH37290 AAX08098 AAX08099 AAX93190 BAA28271 BAA28273 BAG36730 CAA06878 CAA07552 EAW71019 | ||||||||||
RNA Seq Atlas | 3769 | ||||||||||