1. Gene
  2. KCNK10 - potassium two pore domain channel subfamily K member 10 Gene

KCNK10 - potassium two pore domain channel subfamily K member 10 Gene

中文名称:钾二孔域通道亚科 K 成员 10

种属: Homo sapiens

同用名: TREK2; TREK-2; K2p10.1; PPP1R97

基因 ID: 54207 | 基因类型: protein coding

关于 KCNK10

Cytogenetic location: 14q31.3 Genomic coordinates (GRCh38): 14:88,180,108-88,326,912 (from NCBI)

This gene has 4 transcripts (splice variants), 288 orthologues and 14 paralogues. Biased expression in brain (RPKM 1.7), duodenum (RPKM 1.4) and 8 other tissues.

功能概要

由该基因编码的蛋白质属于含有两个成孔 P 结构域的钾通道蛋白家族。该通道是一个开放式整流器,主要在生理 K+ 浓度下传递外向电流,并受到花生四烯酸的强烈刺激,并在较小程度上受到膜拉伸、细胞内酸化和全身麻醉的刺激。已经为该基因鉴定了几种编码不同亚型的可变剪接转录物变体。[RefSeq 提供,2008 年 9 月]

The protein encoded by this gene belongs to the family of Potassium Channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations, and is stimulated strongly by arachidonic acid and to a lesser degree by membrane stretching, intracellular acidification, and general anaesthetics. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Sep 2008]

KCNK10 基因产物(3)

mRNA Protein Name
NM_021161.5 NP_066984.1 potassium channel subfamily K member 10 isoform 1 precursor
NM_138317.3 NP_612190.1 potassium channel subfamily K member 10 isoform 2
NM_138318.3 NP_612191.1 potassium channel subfamily K member 10 isoform 3
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables mechanosensitive potassium channel activity IDA
IDA: 通过直接分析推断
38605031 GOA
enables outward rectifier potassium channel activity IDA
IDA: 通过直接分析推断
26919430 GOA
enables potassium ion leak channel activity IDA
IDA: 通过直接分析推断
26919430 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cellular response to arachidonate IDA
IDA: 通过直接分析推断
26919430 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

KCNK10 蛋白结构

Ion_trans_2

Ion_trans_2: Ion channel (147 - 206)

Ion_trans_2

Ion_trans_2: Ion channel (244 - 323)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 538 a.a.
蛋白主名 其他名称

potassium channel subfamily K member 10

2P domain potassium channel TREK2

关联疾病

疾病名称 别名
Birk-Barel Syndrome

Birk-Barel Mental Retardation Dysmorphism Syndrome

BIBARS

Mental Retardation With Hypotonia And Facial Dysmorphism

Intellectual Disability-Hypotonia-Facial Dysmorphism Syndrome

Kcnk9 Imprinting Syndrome

Brain Glioblastoma Multiforme

Brain Glioblastoma

Glioblastoma Multiforme Of Brain

Glioblastoma Nos

Migraine With Aura

Classic Migraine

Migraine With Typical Aura

Migraine Accompagnée

Complicated Migraine

Classical Migraine

Acute Migraine With Aura

Migraine With Or Without Aura 1

Migraine

Migraine With Or Without Aura, Susceptibility To, 1

Migraine Disorder

Migraine Variant

Migraines

Migraine Disorders

Mgr1

Mgau

Ma

Migraine With Or Without Aura

Classic Migraine

Common Migraine

Disorder, Migraine

Headache Migraine

Headache Migrainous

Migraine Headache

Migraine Syndrome

Headache Including Migraine

Migraine, Susceptibility To

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta KCNK10 VGNC VGNC:73994
Felis catus KCNK10 VGNC VGNC:67919
Mus musculus KCNK10 MGD MGI:1919508
Canis familiaris KCNK10 VGNC VGNC:42270
Bos taurus KCNK10 VGNC VGNC:30466
Rattus norvegicus KCNK10 RGD RGD:619732