1. Gene
  2. CHP1 - calcineurin like EF-hand protein 1 Gene

CHP1 - calcineurin like EF-hand protein 1 Gene

中文名称:神经钙蛋白样 EF-手蛋白 1

种属: Homo sapiens

同用名: CHP; p22; p24; SPAX9; Sid470p; SLC9A1BP

基因 ID: 11261 | 基因类型: protein coding

关于 CHP1

Cytogenetic location: 15q15.1 Genomic coordinates (GRCh38): 15:41,231,268-41,281,887 (from NCBI)

This gene has 9 transcripts (splice variants), 230 orthologues, 8 paralogues and is associated with 1 phenotype. Ubiquitous expression in colon (RPKM 59.2), liver (RPKM 56.3) and 25 other tissues.

功能概要

该基因编码一种与 Na+/H+ 交换器 NHE1 结合的磷蛋白。该蛋白作为支持 NHE 家族成员生理活性的必需辅助因子,可能在 NHE1 的促有丝分裂调节中发挥作用。该蛋白质与钙调神经磷酸酶 B 和钙调蛋白具有相似性,并且还已知它是钙调神经磷酸酶活性的内源性抑制剂。[RefSeq 提供,2008 年 7 月]

This gene encodes a phosphoprotein that binds to the Na+/H+ exchanger NHE1. This protein serves as an essential cofactor which supports the physiological activity of NHE family members and may play a role in the mitogenic regulation of NHE1. The protein shares similarity with Calcineurin B and Calmodulin and it is also known to be an endogenous inhibitor of Calcineurin activity. [provided by RefSeq, Jul 2008]

CHP1 基因产物(1)

mRNA Protein Name
NM_007236.5 NP_009167.1 calcineurin B homologous protein 1
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables calcium ion binding IDA
IDA: 通过直接分析推断
15035633 GOA
enables calcium-dependent protein binding IDA
IDA: 通过直接分析推断
15035633 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
8901634 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in plasma membrane IDA
IDA: 通过直接分析推断
11350981 GOA
located in plasma membrane IMP
IMP: 通过突变表型推断
29379881 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

CHP1 蛋白结构

EF-hand_7

EF-hand_7: EF-hand domain pair (114 - 178)

  • 0
  • 100
  • 195 a.a.
蛋白主名 其他名称

calcineurin B homologous protein 1

EF-hand calcium-binding domain-containing protein p22

CHP1 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
CHP1 Q99653 SLC9A1 Homo sapiens P19634 31912575
种属内
CHP1 Q99653 SLC9A1 Homo sapiens P19634
ITC
31912575
种属内
CHP1 Q99653 SLC9A1 Homo sapiens P19634
MST
31912575
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
Spastic Ataxia 9, Autosomal Recessive

SPAX9

Lichtenstein-Knorr Syndrome

Scar19

LIKNS

Autosomal Recessive Spinocerebellar Ataxia 19

Spinocerebellar Ataxia, Autosomal Recessive 19

Progressive Autosomal Recessive Ataxia-Deafness Syndrome

Progressive Autosomal Recessive Ataxia-Sensorineural Hearing Loss Syndrome

Spinocerebellar Ataxia, Autosomal Recessive, 19

Cataract 3, Multiple Types

Cataract 3 Multiple Types

CTRCT3

Cca2

Cataract, Congenital, Cerulean Type, 2

Cataract 3, Multiple Types, With Or Without Microcornea

Cataract 3 Multiple Types With Or Without Microcornea

Congenital Cerulean Type Cataract 2

Congenital Cataract Blue Dot Type 2

Congenital Cataract Cerulean Type 2

Cspc

Sutural Cataract With Punctate And Cerulean Opacities

Spastic Paraparesis
Spastic Ataxia

Spax

Ataxia, Spastic

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
Mus musculus CHP1 MGD MGI:1927185
Canis familiaris CHP1 VGNC VGNC:39227
Bos taurus CHP1 VGNC VGNC:27310
Rattus norvegicus CHP1 RGD RGD:620447
Felis catus CHP1 VGNC VGNC:81003