Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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8645 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Potassium two pore domain channel subfamily K member 5 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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KCNK5 |
SynonymsGene synonyms aliases
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K2p5.1, KCNK5b, TASK-2, TASK2 |
ChromosomeChromosome number
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6 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6p21.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The message for this gene is mainly expressed in the cortical distal tubules and collecting ducts of the kidney. The protein is highly sensitive to external pH and this, in combination with its expression pattern, suggests it may play an important role in renal potassium transport. [provided by RefSeq, Jul 2008] |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
O95279 |
Protein name |
Potassium channel subfamily K member 5 (Acid-sensitive potassium channel protein TASK-2) (TWIK-related acid-sensitive K(+) channel 2) |
Protein function |
pH-dependent, voltage insensitive, outwardly rectifying potassium channel. Outward rectification is lost at high external K(+) concentrations. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF07885 |
Ion_trans_2 |
60 → 138 |
Ion channel |
Family |
PF07885 |
Ion_trans_2 |
160 → 251 |
Ion channel |
Family |
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Sequence |
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Sequence length |
499 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Coronary artery disease |
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1, Coronary Artery Disease |
rs137852988, rs121918313, rs-1, rs121918529, rs121918531, rs137852340, rs405509, rs1555800701, rs1215189537 |
23202125, 29212778 |
Migraine |
Migraine Disorders |
rs794727411 |
23793025, 27322543, 27182965 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Grand mal status epilepticus |
Grand Mal Status Epilepticus |
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19220408 |
Nonconvulsive status epilepticus |
Non-Convulsive Status Epilepticus |
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19220408 |
Petit mal status |
Petit mal status |
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19220408 |
Status epilepticus |
Status Epilepticus, Complex Partial Status Epilepticus, Status Epilepticus, Subclinical |
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19220408 |
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