1. Gene
  2. KCNA3 - potassium voltage-gated channel subfamily A member 3 Gene

KCNA3 - potassium voltage-gated channel subfamily A member 3 Gene

中文名称:钾电压门控通道亚家族 A 成员 3

种属: Homo sapiens

同用名: MK3; HGK5; HLK3; PCN3; HPCN3; KV1.3; HUKIII

基因 ID: 3738 | 基因类型: protein coding

关于 KCNA3

Cytogenetic location: 1p13.3 Genomic coordinates (GRCh38): 1:110,653,560-110,674,940 (from NCBI)

This gene has 6 transcripts (splice variants), 249 orthologues and 31 paralogues. Broad expression in lymph node (RPKM 7.8), appendix (RPKM 6.0) and 17 other tissues.

功能概要

从功能和结构的角度来看,钾通道代表了最复杂的一类电压门控离子通道。它们的不同功能包括调节神经递质释放、心率、胰岛素分泌、神经元兴奋性、上皮电解质转运、平滑肌收缩和细胞体积。四种序列相关的钾通道基因——shaker、shaw、shab 和 shal——已在果蝇中被鉴定出来,并且每一种都被证明具有人类同系物。该基因编码钾通道、电压门控、摇床相关亚家族的成员。该成员包含六个跨膜结构域,在第四部分中具有振动型重复序列。它属于延迟整流器类,其成员允许神经细胞在动作电位后有效地复极化。它在 T 细胞增殖和激活中起重要作用。该基因似乎是无内含子的,它与 1 号染色体上的 KCNA2 和 KCNA10 基因聚集在一起。[RefSeq 提供,2008 年 7 月]

Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, Insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related Potassium Channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the Potassium Channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, members of which allow nerve cells to efficiently repolarize following an action potential. It plays an essential role in T-cell proliferation and activation. This gene appears to be intronless and it is clustered together with KCNA2 and KCNA10 genes on chromosome 1. [provided by RefSeq, Jul 2008]

KCNA3 基因产物(1)

mRNA Protein Name
NM_002232.5 NP_002223.3 potassium voltage-gated channel subfamily A member 3
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
18818304 GOA
NOT enables voltage-gated potassium channel activity IDA
IDA: 通过直接分析推断
8774427 GOA
enables voltage-gated potassium channel activity IDA
IDA: 通过直接分析推断
1547020 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in perinuclear region of cytoplasm IDA
IDA: 通过直接分析推断
8774427 GOA
located in plasma membrane IDA
IDA: 通过直接分析推断
8774427 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

KCNA3 蛋白结构

BTB_2

BTB_2: BTB/POZ domain (106 - 196)

Ion_trans

Ion_trans: Ion transport protein (298 - 479)

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

potassium voltage-gated channel subfamily A member 3

potassium channel 3

KCNA3 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
KCNA3 P22001 BAX Homo sapiens Q07812 18818304
种属内
KCNA3 P22001 KCNA1 Homo sapiens Q09470 32296183
种属内
KCNA3 P22001 DOLK Homo sapiens Q9UPQ8 32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Alzheimer Disease 17

AD17

Alzheimer'S Disease 17

Alzheimer Disease 17, Late-Onset

Alzheimer Disease 17, Late Onset

Diamond-Blackfan Anemia 3

DBA3

Anemia, Diamond-Blackfan, 3

Rps24-Related Diamond-Blackfan Anemia

Anemia Diamond-Blackfan 3

Anemia, Diamond-Blackfan, Type 3

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
Bos taurus KCNA3 VGNC VGNC:30423
Mus musculus KCNA3 MGD MGI:96660
Canis familiaris KCNA3 VGNC VGNC:42230
Macaca mulatta KCNA3 VGNC VGNC:73964
Rattus norvegicus KCNA3 RGD RGD:2951
Felis catus KCNA3 VGNC VGNC:67892
Others KCNA3 NCBI