1. Gene
  2. MED17 - mediator complex subunit 17 Gene

MED17 - mediator complex subunit 17 Gene

中文名称:介体复合体亚基 17

种属: Homo sapiens

同用名: SRB4; CRSP6; CRSP77; DRIP80; TRAP80

基因 ID: 9440 | 基因类型: protein coding

关于 MED17

Cytogenetic location: 11q21 Genomic coordinates (GRCh38): 11:93,784,282-93,814,963 (from NCBI)

This gene has 29 transcripts (splice variants), 206 orthologues and is associated with 3 phenotypes. Ubiquitous expression in thyroid (RPKM 8.7), ovary (RPKM 8.2) and 25 other tissues.

功能概要

基因转录的激活是一个多步骤过程,由识别 DNA 中转录增强子位点的因素触发。这些因子与共激活因子一起通过 RNA 聚合酶 II 装置指导转录起始。该基因编码的蛋白质是 CRSP (SP1 激活所需的辅因子) 复合物的一个亚基,它与 TFIID 一起是 SP1 有效激活所必需的。这种蛋白质也是其他多亚基复合物的组成部分,例如甲状腺激素受体- (TR-) 相关蛋白,它与 TR 相互作用并促进 TR 在 DNA 模板上与起始因子和辅因子一起发挥功能。[RefSeq 提供,2008 年 7 月]

The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. [provided by RefSeq, Jul 2008]

MED17 基因产物(1)

mRNA Protein Name
NM_004268.5 NP_004259.3 mediator of RNA polymerase II transcription subunit 17
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 nuclear receptor coactivator activity IDA
IDA: 通过直接分析推断
12218053 GOA
enables nuclear thyroid hormone receptor binding IDA
IDA: 通过直接分析推断
10198638 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
12584197 GOA
enables transcription coactivator activity IDA
IDA: 通过直接分析推断
12037571 GOA
enables transcription coregulator activity IDA
IDA: 通过直接分析推断
10198638 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of core mediator complex IPI
IPI: 通过物理相互作用推断
24882805 GOA
part of mediator complex IDA
IDA: 通过直接分析推断
10198638 GOA
located in nucleus IDA
IDA: 通过直接分析推断
10235267 GOA
part of transcription regulator complex IDA
IDA: 通过直接分析推断
9989412 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

MED17 蛋白结构

Med17

Med17: Subunit 17 of Mediator complex (9 - 459)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 600
  • 651 a.a.
蛋白主名 其他名称

mediator of RNA polymerase II transcription subunit 17

ARC77

MED17 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
Cross MED17 Q9NVC6 Med30 Mus musculus Q9CQI9
Pull Down
12584197
Cross MED17 Q9NVC6 Med30 Mus musculus Q9CQI9
Anti Tag CoIP
24882805
Intra MED17 Q9NVC6 MED27 Homo sapiens Q6P2C8
Anti Tag CoIP
33961781
Intra MED17 Q9NVC6 MED27 Homo sapiens Q6P2C8
Anti Tag CoIP
24882805
Intra MED17 Q9NVC6 MED27 Homo sapiens Q6P2C8
Anti Tag CoIP
35271311
Intra MED17 Q9NVC6 MED27 Homo sapiens Q6P2C8
TAP
24981860
Intra MED17 Q9NVC6 MED6 Homo sapiens O75586
Anti Tag CoIP
33961781
Intra MED17 Q9NVC6 MED6 Homo sapiens O75586
Anti Tag CoIP
24882805
Intra MED17 Q9NVC6 MED22 Homo sapiens Q15528
Anti Tag CoIP
33961781
Intra MED17 Q9NVC6 MED22 Homo sapiens Q15528
Pull Down
12584197
Intra MED17 Q9NVC6 MED22 Homo sapiens Q15528
TAP
24981860
Intra MED17 Q9NVC6 MED22 Homo sapiens Q15528
Anti Tag CoIP
24882805
Intra MED17 Q9NVC6 MED28 Homo sapiens Q9H204
TAP
24981860
Intra MED17 Q9NVC6 MED28 Homo sapiens Q9H204
Anti Tag CoIP
33961781
Intra MED17 Q9NVC6 MED28 Homo sapiens Q9H204
Anti Tag CoIP
35271311
Cross MED17 Q9NVC6 Med11 Mus musculus Q9D8C6
Anti Tag CoIP
24882805
Cross MED17 Q9NVC6 Med8 Mus musculus Q9D7W5
Anti Tag CoIP
24882805
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
Microcephaly, Postnatal Progressive, With Seizures And Brain Atrophy

Infantile Cerebral And Cerebellar Atrophy With Postnatal Progressive Microcephaly

Postnatal Progressive Microcephaly, Seizures, And Brain Atrophy

MCPHSBA

Mucinous Adenofibroma
Palindromic Rheumatism

Hench'S Syndrome

Hench-Rosenberg Syndrome

Palindromic Rheumatism Syndrome

Palindromic Arthritis

Microcephaly, Seizures, And Developmental Delay

MCSZ

Developmental And Epileptic Encephalopathy 10

Epileptic Encephalopathy, Early Infantile, 10

Eiee10

Dee10

Early Infantile Epileptic Encephalopathy 10

Hermansky-Pudlak Syndrome 3

HPS3

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial

Delta Storage Pool Disease

Hermansky-Pudlak Syndrome, Type 3

Platelet Storage Pool Deficiency

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

Opitz-Kaveggia Syndrome

Fg Syndrome

Fgs1

Fgs

Keller Syndrome

OKS

Fg Syndrome 1

Fg Syndrome Type 1

Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, And Partial Agenesis Of Corpus Callosum

Intellectual Disability, Large Head, Imperforate Anus, Congenital Hypotonia, And Partial Agenesis Of Corpus Callosum

Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, And Partial Agenesis Of The Corpus Callosum

Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly

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 MED17 MGD MGI:2182585
Canis familiaris MED17 VGNC VGNC:52266
Rattus norvegicus MED17 RGD RGD:1311120
Felis catus MED17 VGNC VGNC:103133
Bos taurus MED17 VGNC VGNC:56273