Q99712 (IRK15_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 118.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: ATP-sensitive inward rectifier potassium channel 15 Alternative name(s): Inward rectifier K(+) channel Kir1.3 Inward rectifier K(+) channel Kir4.2 Potassium channel, inwardly rectifying subfamily J member 15 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 375 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. |
| Subunit structure | Interacts with INADL. Ref.7 |
| Subcellular location | |
| Sequence similarities | Belongs to the inward rectifier-type potassium channel (TC 1.A.2.1) family. KCNJ15 subfamily. [View classification] |
Ontologies
| Keywords | |
|---|---|
| Biological process | Ion transport Potassium transport Transport |
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| Ligand | Potassium |
| Molecular function | Ion channel Voltage-gated channel |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | synaptic transmission Traceable author statement. Source: Reactome |
| Cellular_component | integral to plasma membrane Traceable author statement Ref.2. Source: ProtInc |
| Molecular_function | inward rectifier potassium channel activity Traceable author statement Ref.2. Source: ProtInc |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 375 | 375 | ATP-sensitive inward rectifier potassium channel 15 | PRO_0000154972 | |||||
Regions | |||||||||
| Topological domain | 1 – 63 | 63 | Cytoplasmic By similarity | ||||||
| Transmembrane | 64 – 88 | 25 | Helical; Name=M1; By similarity | ||||||
| Topological domain | 89 – 113 | 25 | Extracellular By similarity | ||||||
| Intramembrane | 114 – 125 | 12 | Helical; Pore-forming; Name=H5; By similarity | ||||||
| Intramembrane | 126 – 132 | 7 | Pore-forming; By similarity | ||||||
| Topological domain | 133 – 141 | 9 | Extracellular By similarity | ||||||
| Transmembrane | 142 – 163 | 22 | Helical; Name=M2; By similarity | ||||||
| Topological domain | 164 – 375 | 212 | Cytoplasmic By similarity | ||||||
| Motif | 127 – 132 | 6 | Selectivity filter By similarity | ||||||
Sites | |||||||||
| Site | 157 | 1 | Role in the control of polyamine-mediated channel gating and in the blocking by intracellular magnesium By similarity | ||||||
Natural variations | |||||||||
| Natural variant | 30 | 1 | M → L. Corresponds to variant rs3746875 [ dbSNP | Ensembl ]. | VAR_025523 | |||||
| Natural variant | 71 | 1 | A → T in a breast cancer sample; somatic mutation. Ref.8 | VAR_036427 | |||||
| Natural variant | 98 | 1 | G → D. Ref.2 Ref.3 Corresponds to variant rs2230033 [ dbSNP | Ensembl ]. | VAR_019728 | |||||
Experimental info | |||||||||
| Sequence conflict | 235 | 1 | V → A in CAA71734. Ref.1 | ||||||
| Sequence conflict | 245 | 1 | S → G in BAA13326. Ref.3 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "A new inward rectifier potassium channel gene (KCNJ15) localized on chromosome 21 in the Down syndrome chromosome region 1 (DCR1)." Gosset P., Ghezala G.A., Korn B., Yaspo M.-L., Poutska A., Lehrach H., Sinet P.-M., Creau N. Genomics 44:237-241(1997) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. |
| [2] | "Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3)." Shuck M.E., Piser T.M., Bock J.H., Slightom J.L., Lee K.S., Bienkowski M.J. J. Biol. Chem. 272:586-593(1997) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT ASP-98. Tissue: Kidney. |
| [3] | Ohira M., Seki N., Nagase T., Suzuki E., Nomura N., Ohara O., Hattori M., Sakaki Y., Eki T., Murakami Y., Saito T., Ichikawa H., Ohki M. Submitted (JAN-1997) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT ASP-98. Tissue: Kidney. |
| [4] | "The DNA sequence of human chromosome 21." Hattori M., Fujiyama A., Taylor T.D., Watanabe H., Yada T., Park H.-S., Toyoda A., Ishii K., Totoki Y., Choi D.-K., Groner Y., Soeda E., Ohki M., Takagi T., Sakaki Y., Taudien S., Blechschmidt K., Polley A. Yaspo M.-L.Nature 405:311-319(2000) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [5] | Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. Venter J.C.Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [6] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Kidney. |
| [7] | "CIPP, a novel multivalent PDZ domain protein, selectively interacts with Kir4.0 family members, NMDA receptor subunits, neurexins, and neuroligins." Kurschner C., Mermelstein P.G., Holden W.T., Surmeier D.J. Mol. Cell. Neurosci. 11:161-172(1998) [PubMed] [Europe PMC] [Abstract] Cited for: INTERACTION WITH INADL. |
| [8] | "The consensus coding sequences of human breast and colorectal cancers." Sjoeblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D., Mandelker D., Leary R.J., Ptak J., Silliman N., Szabo S., Buckhaults P., Farrell C., Meeh P., Markowitz S.D., Willis J., Dawson D., Willson J.K.V. Velculescu V.E.Science 314:268-274(2006) [PubMed] [Europe PMC] [Abstract] Cited for: VARIANT [LARGE SCALE ANALYSIS] THR-71. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | Y10745 mRNA. Translation: CAA71734.1. U73191 mRNA. Translation: AAC50922.1. D87291 mRNA. Translation: BAA13326.1. AP001434 Genomic DNA. No translation available. CH471079 Genomic DNA. Translation: EAX09683.1. CH471079 Genomic DNA. Translation: EAX09684.1. BC013327 mRNA. Translation: AAH13327.1. |
| IPI | IPI00064771. |
| RefSeq | NP_001263364.1. NM_001276435.1. NP_001263365.1. NM_001276436.1. NP_001263366.1. NM_001276437.1. NP_001263367.1. NM_001276438.1. NP_001263368.1. NM_001276439.1. NP_002234.2. NM_002243.4. NP_733932.1. NM_170736.2. NP_733933.1. NM_170737.2. |
| UniGene | Hs.411299. |
3D structure databases | |
| ProteinModelPortal | Q99712. |
| ModBase | Search... |
Protein-protein interaction databases | |
| MINT | MINT-103775. |
| STRING | 9606.ENSP00000331698. |
PTM databases | |
| PhosphoSite | Q99712. |
Polymorphism databases | |
| DMDM | 77416869. |
Proteomic databases | |
| PaxDb | Q99712. |
| PRIDE | Q99712. |
Protocols and materials databases | |
| DNASU | 3772. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000328656; ENSP00000331698; ENSG00000157551. ENST00000398930; ENSP00000381904; ENSG00000157551. ENST00000398932; ENSP00000381905; ENSG00000157551. ENST00000398934; ENSP00000381907; ENSG00000157551. ENST00000398938; ENSP00000381911; ENSG00000157551. |
| GeneID | 3772. |
| KEGG | hsa:3772. |
| UCSC | uc002ywv.3. human. |
Organism-specific databases | |
| CTD | 3772. |
| GeneCards | GC21P039529. |
| HGNC | HGNC:6261. KCNJ15. |
| HPA | HPA016702. |
| MIM | 602106. gene. |
| neXtProt | NX_Q99712. |
| PharmGKB | PA30046. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG289501. |
| HOGENOM | HOG000237326. |
| HOVERGEN | HBG006178. |
| InParanoid | Q99712. |
| KO | K05008. |
| OMA | VRVANMR. |
| OrthoDB | EOG41JZCP. |
| PhylomeDB | Q99712. |
Enzyme and pathway databases | |
| Reactome | REACT_13685. Neuronal System. |
Gene expression databases | |
| ArrayExpress | Q99712. |
| Bgee | Q99712. |
| CleanEx | HS_KCNJ14. HS_KCNJ15. |
| Genevestigator | Q99712. |
| GermOnline | ENSG00000157551. Homo sapiens. |
Family and domain databases | |
| Gene3D | 2.60.40.1400. 1 hit. |
| InterPro | IPR014756. Ig_E-set. IPR016449. K_chnl_inward-rec_Kir. IPR003270. K_chnl_inward-rec_Kir1.3. IPR013518. K_chnl_inward-rec_Kir_cyto. [Graphical view] |
| PANTHER | PTHR11767. PTHR11767. 1 hit. PTHR11767:SF20. PTHR11767:SF20. 1 hit. |
| Pfam | PF01007. IRK. 1 hit. [Graphical view] |
| PIRSF | PIRSF005465. GIRK_kir. 1 hit. |
| PRINTS | PR01323. KIR13CHANNEL. PR01320. KIRCHANNEL. |
| SUPFAM | SSF81296. Ig_E-set. 1 hit. |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 3772. |
| NextBio | 14791. |
| SOURCE | Search... |
Entry information
| Entry name | IRK15_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q99712 Secondary accession number(s): D3DSH5 Q99446 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 21 Human chromosome 21: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with
