1. Gene
  2. HEXIM1 - HEXIM P-TEFb complex subunit 1 Gene

HEXIM1 - HEXIM P-TEFb complex subunit 1 Gene

中文名称:HEXIM P-TEFb 复合亚基 1

种属: Homo sapiens

同用名: CLP1; EDG1; HIS1; MAQ1

基因 ID: 10614 | 基因类型: protein coding

关于 HEXIM1

Cytogenetic location: 17q21.31 Genomic coordinates (GRCh38): 17:45,148,475-45,152,099 (from NCBI)

This gene has 1 transcript (splice variant), 116 orthologues and 1 paralogue.

功能概要

该基因的表达由六亚甲基双乙酰胺在血管平滑肌细胞中诱导。该基因没有内含子。[RefSeq 提供,2008 年 7 月]

Expression of this gene is induced by hexamethylene-bis-acetamide in vascular smooth muscle cells. This gene has no introns. [provided by RefSeq, Jul 2008]

HEXIM1 基因产物(1)

mRNA Protein Name
NM_006460.3 NP_006451.1 protein HEXIM1
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 7SK snRNA binding IDA
IDA: 通过直接分析推断
12832472 GOA
enables P-TEFb complex binding IDA
IDA: 通过直接分析推断
18249148 GOA
enables cyclin-dependent protein serine/threonine kinase inhibitor activity IDA
IDA: 通过直接分析推断
14580347 GOA
enables identical protein binding IPI
IPI: 通过物理相互作用推断
17724342 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
12832472 GOA
enables protein kinase inhibitor activity IDA
IDA: 通过直接分析推断
28431135 GOA
enables snRNA binding IDA
IDA: 通过直接分析推断
14580347 GOA
enables transcription regulator inhibitor activity IDA
IDA: 通过直接分析推断
14580347 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of 7SK snRNP IDA
IDA: 通过直接分析推断
18249148 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
12581153 GOA
located in nucleus IDA
IDA: 通过直接分析推断
12581153 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

HEXIM1 蛋白结构

HEXIM

HEXIM: Hexamethylene bis-acetamide-inducible protein (164 - 302)

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

protein HEXIM1

HMBA-inducible

HEXIM1 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
Intra HEXIM1 O94992 CDK9 Homo sapiens P50750
Anti Tag CoIP
33961781
Intra HEXIM1 O94992 CDK9 Homo sapiens P50750
TAP
24981860
Intra HEXIM1 O94992 CDK9 Homo sapiens P50750
Anti Bait CoIP
25470060
Intra HEXIM1 O94992 CDK9 Homo sapiens P50750
Anti Bait CoIP
18483487
Intra HEXIM1 O94992 CDK9 Homo sapiens P50750
Pull Down
18483487
Intra HEXIM1 O94992 LARP7 Homo sapiens Q4G0J3
Anti Tag CoIP
28514442
Intra HEXIM1 O94992 LARP7 Homo sapiens Q4G0J3
Pull Down
18483487
Intra HEXIM1 O94992 LARP7 Homo sapiens Q4G0J3
Anti Bait CoIP
18281698
Intra HEXIM1 O94992 LARP7 Homo sapiens Q4G0J3
Anti Bait CoIP
18483487
Intra HEXIM1 O94992 LARP7 Homo sapiens Q4G0J3
Anti Tag CoIP
33961781
Intra HEXIM1 O94992 LARP7 Homo sapiens Q4G0J3
Anti Bait CoIP
25470060
Intra HEXIM1 O94992 CCNT1 Homo sapiens O60563
Fluorescence Spectr
17724342
Intra HEXIM1 O94992 CCNT1 Homo sapiens O60563
Anti Tag CoIP
17724342
Intra HEXIM1 O94992 CCNT1 Homo sapiens O60563
Anti Tag CoIP
33961781
Intra HEXIM1 O94992 CCNT1 Homo sapiens O60563
Anti Bait CoIP
18483487
Intra HEXIM1 O94992 CCNT1 Homo sapiens O60563
Anti Bait CoIP
18281698
Intra HEXIM1 O94992 CCNT1 Homo sapiens O60563
Anti Tag CoIP
28514442
Intra HEXIM1 O94992 HEXIM2 Homo sapiens Q96MH2
Anti Tag CoIP
33961781
Intra HEXIM1 O94992 HEXIM2 Homo sapiens Q96MH2
Anti Tag CoIP
28514442
Intra HEXIM1 O94992 HEXIM2 Homo sapiens Q96MH2
Validated Y2H
32296183
Intra HEXIM1 O94992 TERF2 Homo sapiens Q15554
Pull Down
21044950
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
Nut Midline Carcinoma

Nuclear Protein In Testis Midline Carcinoma

Nmc

Immune Deficiency Disease

Immunodeficiency

Primary Immunodeficiency

Primary Immunodeficiency Disease

Immunologic Deficiency Syndromes

Hypoimmunity

Immune Deficiency Disorder

Immunodeficiency Syndrome

Immune Disorder

Primary Immune Deficiency Disorder

Immune System Diseases

Human Immunodeficiency Virus Infection

Hiv - [Human Immunodeficiency Virus Infection]

Hiv Positive Nos

Hiv Disease

Acquired Immune Deficiency Syndrome-Related Complex

Aids-Like Syndrome

Aids-Related Complex Nos

Arc - [Aids-Related Complex]

Immunodeficiency Due To Human Immunodeficiency Virus Infection

Unspecified Human Immunodeficiency Virus Disease

Hiv Disease Nos

Human Immunodeficiency Virus Positive Nos

Hiv Nos

Deficiency Of Complement Initial Pathway

Deficiency Of Complement Terminal Pathway

Cfdd - [Complement Factor D Deficiency]

Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency

Nonfamilial Hypogammaglobulinaemia

Common Variable Immune Deficiency

Nonfamilial Agammaglobulinaemia

Common Variable Agammaglobulinaemia

Agammaglobulinaemia Nos

Agammaglobulinaemia Antibody Deficiency Syndrome

Hypogammaglobulinaemia Antibody Deficiency Syndrome

Acquired Agammaglobulinaemia Nos

Hypogammaglobulinaemia Nos

Hyper Igm

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
Felis catus HEXIM1 VGNC VGNC:62803
Macaca mulatta HEXIM1 VGNC VGNC:104615
Mus musculus HEXIM1 MGD MGI:2385923
Rattus norvegicus HEXIM1 RGD RGD:1559851
Bos taurus HEXIM1 VGNC VGNC:29826
Canis familiaris HEXIM1 VGNC VGNC:41670