1. Gene
  2. KCNAB3 - potassium voltage-gated channel subfamily A regulatory beta subunit 3 Gene

KCNAB3 - potassium voltage-gated channel subfamily A regulatory beta subunit 3 Gene

中文名称:钾电压门控通道亚家族 A 调节 β 亚基 3

种属: Homo sapiens

同用名: AKR6A9; KCNA3B; KCNA3.1B; KV-BETA-3

基因 ID: 9196 | 基因类型: protein coding

关于 KCNAB3

Cytogenetic location: 17p13.1 Genomic coordinates (GRCh38): 17:7,921,859-7,929,856 (from NCBI)

This gene has 6 transcripts (splice variants), 246 orthologues and 16 paralogues. Broad expression in endometrium (RPKM 5.0), brain (RPKM 1.9) and 18 other tissues.

功能概要

该基因编码钾通道、电压门控、摇床相关亚家族的成员。编码的蛋白质是 β 亚基之一,它是与功能性 Kv-α 亚基相关的辅助蛋白。编码的蛋白质与钾电压门控通道、摇床相关亚家族、成员 5 基因产物形成异二聚体,并调节 alpha 亚基的活性。[RefSeq 提供,2012 年 5 月]

This gene encodes a member of the Potassium Channel, voltage-gated, shaker-related subfamily. The encoded protein is one of the beta subunits, which are auxiliary proteins associating with functional Kv-alpha subunits. The encoded protein forms a heterodimer with the potassium voltage-gated channel, shaker-related subfamily, member 5 gene product and regulates the activity of the alpha subunit. [provided by RefSeq, May 2012]

KCNAB3 基因产物(1)

mRNA Protein Name
NM_004732.4 NP_004723.2 voltage-gated potassium channel subunit beta-3

KCNAB3 蛋白结构

Aldo_ket_red

Aldo_ket_red: Aldo/keto reductase family (93 - 395)

  • 0
  • 100
  • 200
  • 300
  • 404 a.a.
蛋白主名 其他名称

voltage-gated potassium channel subunit beta-3

K(+) channel subunit beta-3

KCNAB3 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
KCNAB3 O43448 PLEKHF2 Homo sapiens Q9H8W4 32296183
种属内
KCNAB3 O43448 PLEKHF2 Homo sapiens Q9H8W4 32296183
种属内
KCNAB3 O43448 PLEKHF2 Homo sapiens Q9H8W4 32296183
种属内
KCNAB3 O43448 GMDS Homo sapiens O60547 32296183
种属内
KCNAB3 O43448 GMDS Homo sapiens O60547 32296183
种属内
KCNAB3 O43448 GMDS Homo sapiens O60547 32296183
种属内
KCNAB3 O43448 KCNAB2 Homo sapiens Q13303 33961781
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
Cone-Rod Dystrophy 6

CORD6

Retinal Cone Dystrophy 2

Rcd2

Dystrophy, Cone-Rod, Type 6

Retinitis Pigmentosa 6

Progressive Cone Degeneration

Cone Dystrophy

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 KCNAB3 VGNC VGNC:30429
Canis familiaris KCNAB3 VGNC VGNC:53420
Macaca mulatta KCNAB3 VGNC VGNC:73968
Mus musculus KCNAB3 MGD MGI:1336208
Felis catus KCNAB3 VGNC VGNC:67896
Rattus norvegicus KCNAB3 RGD RGD:61830