Q9UNX9 (IRK14_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 93.
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 14 Alternative name(s): Inward rectifier K(+) channel Kir2.4 Short name=IRK-4 Potassium channel, inwardly rectifying subfamily J member 14 | ||||
| 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 | 436 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. KCNJ14 gives rise to low-conductance channels with a low affinity to the channel blockers Barium and Cesium By similarity. |
| Subcellular location | |
| Tissue specificity | Expressed preferentially in retina. Ref.1 |
| Sequence similarities | Belongs to the inward rectifier-type potassium channel (TC 1.A.2.1) family. KCNJ14 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 | dendrite Inferred from electronic annotation. Source: Compara neuronal cell bodyInferred from electronic annotation. Source: Compara voltage-gated potassium channel complexTraceable author statement PubMed 9592090. Source: ProtInc |
| Molecular_function | inward rectifier potassium channel activity Traceable author statement PubMed 9592090. Source: ProtInc |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 436 | 436 | ATP-sensitive inward rectifier potassium channel 14 | PRO_0000154968 | |||||
Regions | |||||||||
| Topological domain | 1 – 86 | 86 | Cytoplasmic By similarity | ||||||
| Transmembrane | 87 – 111 | 25 | Helical; Name=M1; By similarity | ||||||
| Topological domain | 112 – 133 | 22 | Extracellular By similarity | ||||||
| Intramembrane | 134 – 145 | 12 | Helical; Pore-forming; Name=H5; By similarity | ||||||
| Intramembrane | 146 – 152 | 7 | Pore-forming; By similarity | ||||||
| Topological domain | 153 – 161 | 9 | Extracellular By similarity | ||||||
| Transmembrane | 162 – 183 | 22 | Helical; Name=M2; By similarity | ||||||
| Topological domain | 184 – 436 | 253 | Cytoplasmic By similarity | ||||||
| Motif | 147 – 152 | 6 | Selectivity filter By similarity | ||||||
Natural variations | |||||||||
| Natural variant | 289 | 1 | R → C. Corresponds to variant rs3745725 [ dbSNP | Ensembl ]. | VAR_034019 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Cloning and functional expression of human retinal Kir2.4, a pH-sensitive inwardly rectifying K+ channel." Hughes B.A., Kumar G., Yuan Y., Swaminathan A., Yan D., Sharma A., Plumley L., Yang-Feng T.L., Swaroop A. Am. J. Physiol. 279:C771-C784(2000) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], CHARACTERIZATION, TISSUE SPECIFICITY. |
| [2] | "Cloning, structure and assignment to chromosome 19q13 of the human Kir2.4 inwardly rectifying potassium channel gene (KCNJ14)." Toepert C., Doring F., Derst C., Daut J., Grzeschik K.H., Karschin A. Mamm. Genome 11:247-249(2000) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]. |
| [3] | "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: Uterus. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF081466 mRNA. Translation: AAD51376.1. AF181988 Genomic DNA. Translation: AAF97619.1. BC035918 mRNA. Translation: AAH35918.1. |
| IPI | IPI00002524. |
| RefSeq | NP_037480.1. NM_013348.3. NP_733838.1. NM_170720.1. |
| UniGene | Hs.590945. Hs.736972. |
3D structure databases | |
| ProteinModelPortal | Q9UNX9. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000341479. |
Polymorphism databases | |
| DMDM | 54036159. |
Proteomic databases | |
| PaxDb | Q9UNX9. |
| PRIDE | Q9UNX9. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000342291; ENSP00000341479; ENSG00000182324. ENST00000391884; ENSP00000375756; ENSG00000182324. |
| GeneID | 3770. |
| KEGG | hsa:3770. |
| UCSC | uc002pje.1. human. |
Organism-specific databases | |
| CTD | 3770. |
| GeneCards | GC19P048958. |
| HGNC | HGNC:6260. KCNJ14. |
| MIM | 603953. gene. |
| neXtProt | NX_Q9UNX9. |
| PharmGKB | PA30045. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG251076. |
| HOGENOM | HOG000237325. |
| HOVERGEN | HBG006178. |
| InParanoid | Q9UNX9. |
| KO | K05007. |
| OMA | PCFSQVA. |
| OrthoDB | EOG48GW3C. |
| PhylomeDB | Q9UNX9. |
Enzyme and pathway databases | |
| Reactome | REACT_13685. Neuronal System. |
Gene expression databases | |
| Bgee | Q9UNX9. |
| CleanEx | HS_KCNJ14. |
| Genevestigator | Q9UNX9. |
| GermOnline | ENSG00000182324. Homo sapiens. |
Family and domain databases | |
| Gene3D | 2.60.40.1400. 1 hit. |
| InterPro | IPR014756. Ig_E-set. IPR016449. K_chnl_inward-rec_Kir. IPR013518. K_chnl_inward-rec_Kir_cyto. [Graphical view] |
| PANTHER | PTHR11767. PTHR11767. 1 hit. |
| Pfam | PF01007. IRK. 1 hit. [Graphical view] |
| PIRSF | PIRSF005465. GIRK_kir. 1 hit. |
| PRINTS | PR01320. KIRCHANNEL. |
| SUPFAM | SSF81296. Ig_E-set. 1 hit. |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 3770. |
| NextBio | 14785. |
| SOURCE | Search... |
Entry information
| Entry name | IRK14_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9UNX9 | ||||||||
| 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 19 Human chromosome 19: 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
