Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
50801
Gene name Gene Name - the full gene name approved by the HGNC.
Potassium two pore domain channel subfamily K member 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KCNK4
Synonyms (NCBI Gene) Gene synonyms aliases
FHEIG, K2p4.1, TRAAK, TRAAK1
Disease Acronyms (UniProt) Disease acronyms from UniProt database
FHEIG
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the TWIK-related arachidonic acid-stimulated two pore potassium channel subfamily. The encoded protein homodimerizes and functions as an outwardly rectifying channel. This channel is regulated by polyunsaturated fatty acids,
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017249 hsa-miR-335-5p Microarray 18185580
MIRT1081852 hsa-miR-1304 CLIP-seq
MIRT1081853 hsa-miR-1827 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005244 Function Voltage-gated ion channel activity IEA
GO:0005267 Function Potassium channel activity IDA 22282805
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0005887 Component Integral component of plasma membrane IMP 22282805
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605720 6279 ENSG00000182450
Protein
UniProt ID Q9NYG8
Protein name Potassium channel subfamily K member 4 (TWIK-related arachidonic acid-stimulated potassium channel protein) (TRAAK) (Two pore potassium channel KT4.1) (K2P4.1) (Two pore K(+) channel KT4.1)
Protein function K(+) channel that conducts voltage-dependent outward rectifying currents upon membrane depolarization. Voltage sensing is coupled to K(+) electrochemical gradient in an 'ion flux gating' mode where outward but not inward ion flow opens the gate.
PDB 3UM7 , 4I9W , 4RUE , 4RUF , 4WFE , 4WFF , 4WFG , 4WFH , 7LJ4 , 7LJ5 , 7LJA , 7LJB
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07885 Ion_trans_2 65 144 Ion channel Family
PF07885 Ion_trans_2 165 259 Ion channel Family
Sequence
MRSTTLLALLALVLLYLVSGALVFRALEQPHEQQAQRELGEVREKFLRAHPCVSDQELGL
LIKEVADALGGGADPETNSTSNSSHSAWDLGSAFFFSGTIITTIGYGNVALRTDAGRLFC
IFYALVGIPLFGILLAGVGDRLGS
SLRHGIGHIEAIFLKWHVPPELVRVLSAMLFLLIGC
LLFVLTPTFVFCYMEDWSKLEAIYFVIVTLTTVGFGDYVAGADPRQDSPAYQPLVWFWIL
LGLAYFASVLTTIGNWLRV
VSRRTRAEMGGLTAQAASWTGTVTARVTQRAGPAAPPPEKE
QPLLPPPPCPAQPLGRPRSPSPPEKAQPPSPPTASALDYPSENLAFIDESSDTQSERGCP
LPRAPRGRRRPNPPRKPVRPRGPGRPRDKGVPV
Sequence length 393
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    TWIK related potassium channel (TREK)
Phase 4 - resting membrane potential
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Brachydactyly Brachydactyly rs121908949, rs28937580, rs121909082, rs104894122, rs863223289, rs863223290, rs104894121, rs1587657302, rs863223292, rs74315386, rs74315387, rs28936397, rs753691079, rs121909348, rs121917852
View all (22 more)
Mental retardation Intellectual Disability rs5742905, rs267607136, rs267607137, rs2131714307, rs267607038, rs267607042, rs80338685, rs137853127, rs80338815, rs28940893, rs387906309, rs121908096, rs121908099, rs587784365, rs121918315
View all (1024 more)
30290154
Nystagmus Nystagmus rs137852207, rs137852208, rs1928435502, rs137852209, rs137852210, rs1929191668, rs137852211, rs137852212, rs2124209414, rs387906720, rs387906721, rs1602791884, rs786205896
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 25809865
Channelopathies Associate 33594261
Developmental Disabilities Associate 30290154, 33594261
digital ulcers Associate 33594261
Epilepsy Associate 30290154
Facial Dysmorphism with Multiple Malformations Associate 30290154
Genetic Diseases Inborn Associate 33594261
Gingival Overgrowth Associate 30290154
Gingivitis Associate 33594261
Hypertrichosis Associate 30290154, 33594261