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  2. MAPK7 - mitogen-activated protein kinase 7 Gene

MAPK7 - mitogen-activated protein kinase 7 Gene

中文名称:丝裂原活化蛋白激酶 7

种属: Homo sapiens

同用名: BMK1; ERK4; ERK5; PRKM7

基因 ID: 5598 | 基因类型: protein coding

关于 MAPK7

Cytogenetic location: 17p11.2 Genomic coordinates (GRCh38): 17:19,377,750-19,383,544 (from NCBI)

This gene has 18 transcripts (splice variants), 193 orthologues and 19 paralogues. Ubiquitous expression in testis (RPKM 7.6), ovary (RPKM 7.0) and 25 other tissues.

功能概要

该基因编码的蛋白质是 MAP 激酶家族的成员。 MAP 激酶作为多种生化信号的整合点,参与多种细胞过程,如增殖、分化、转录调控和发育。该激酶由丝裂原活化蛋白激酶激酶 5 (MAP2K5/MEK5) 特异性激活。它参与各种受体分子的下游信号过程,包括受体型激酶和 G 蛋白偶联受体。响应细胞外信号,该激酶转移到细胞核,在那里它通过磷酸化和激活不同的转录因子来调节基因表达。已经报道了编码两种不同同种型的该基因的四种可变剪接转录物变体。[RefSeq 提供,2008 年 7 月]

The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is specifically activated by mitogen-activated protein kinase kinase 5 (MAP2K5/MEK5). It is involved in the downstream signaling processes of various receptor molecules including receptor type kinases, and G protein-coupled receptors. In response to extracelluar signals, this kinase translocates to cell nucleus, where it regulates gene expression by phosphorylating, and activating different transcription factors. Four alternatively spliced transcript variants of this gene encoding two distinct isoforms have been reported. [provided by RefSeq, Jul 2008]

MAPK7 基因产物(15)

mRNA Protein Name
XM_006721558.4 XP_006721621.1 mitogen-activated protein kinase 7 isoform X1
XM_047436401.1 XP_047292357.1 mitogen-activated protein kinase 7 isoform X1
NM_002749.4 NP_002740.2 mitogen-activated protein kinase 7 isoform 1
NM_139034.3 NP_620603.2 mitogen-activated protein kinase 7 isoform 1
XM_047436406.1 XP_047292362.1 mitogen-activated protein kinase 7 isoform X2
XM_047436405.1 XP_047292361.1 mitogen-activated protein kinase 7 isoform X2
XM_006721559.4 XP_006721622.1 mitogen-activated protein kinase 7 isoform X1
XM_047436407.1 XP_047292363.1 mitogen-activated protein kinase 7 isoform X3
XM_047436404.1 XP_047292360.1 mitogen-activated protein kinase 7 isoform X2
NM_139032.3 NP_620601.1 mitogen-activated protein kinase 7 isoform 2
XM_047436402.1 XP_047292358.1 mitogen-activated protein kinase 7 isoform X1
XM_011523957.4 XP_011522259.1 mitogen-activated protein kinase 7 isoform X4
XM_006721557.4 XP_006721620.1 mitogen-activated protein kinase 7 isoform X1
XM_047436403.1 XP_047292359.1 mitogen-activated protein kinase 7 isoform X1
NM_139033.3 NP_620602.2 mitogen-activated protein kinase 7 isoform 1

MAPK7 蛋白结构

Pkinase

Pkinase: Protein kinase domain (55 - 347)

  • 0
  • 200
  • 400
  • 600
  • 816 a.a.
蛋白主名 其他名称

mitogen-activated protein kinase 7

BMK-1

BMK1 kinase

ERK-5

MAP kinase 7

MAPK 7

big MAP kinase 1

extracellular-signal-regulated kinase 5

MAPK7 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 MAPK7 Q13164 UBE2C Homo sapiens Q5TZN3
Y2H Prey Pooling
25416956
Intra MAPK7 Q13164 UBE2C Homo sapiens Q5TZN3
Validated Y2H
25416956
Intra MAPK7 Q13164 CCDC6 Homo sapiens Q16204
Validated Y2H
32296183
Intra MAPK7 Q13164 PML Homo sapiens P29590
Anti Bait CoIP
20832753
Intra MAPK7 Q13164 PML Homo sapiens P29590
IF
20832753
Intra MAPK7 Q13164 BAG2 Homo sapiens O95816
Anti Tag CoIP
31980649
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
Multiple Endocrine Neoplasia, Type Iia

Multiple Endocrine Neoplasia Type 2a

Sipple Syndrome

Multiple Endocrine Neoplasia Type 2

MEN2A

Men2

Ptc Syndrome

Multiple Endocrine Neoplasia, Type 2

Multiple Endocrine Neoplasia Iia

Men 2a

Multiple Endocrine Neoplasia, Type 2a

Pheochromocytoma And Amyloid-Producing Medullary Thyroid Carcinoma

Multiple Endocrine Neoplasia Ii

Men2 Syndrome

Men-2a Syndrome

Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma

Multiple Neoplasia 2a

Multiple Neoplasia Type 2

Scoliosis
Breast Cancer

Breast Carcinoma

Breast Cancer, Familial

Malignant Neoplasm Of Breast

Male Breast Cancer

Breast Cancer, Susceptibility To

Breast Cancer, Early-Onset

Malignant Tumor Of Breast

Carcinoma Of Male Breast

Breast Cancer, Invasive Ductal

Breast Cancer, Protection Against

Breast Cancer, Somatic

Breast Cancer, Male

Breast Cancer, Lobular, Somatic

Breast Tumor

Mammary Cancer

Mammary Tumor

Malignant Neoplasm Of Male Breast

Mammary Carcinoma

Male Breast Carcinoma

Familial Cancer Of Breast

Invasive Ductal Breast Carcinoma

Breast Cancer Susceptibility

Breast Cancer, Male, Susceptibility To

Breast Cancer, Early-Onset, Susceptibility To

Malignant Tumor Of The Breast

Mammary Neoplasm

Primary Breast Cancer

Neoplasm Of Male Breast

Carcinoma Of Breast

Breast Cancer In Men

Familial Breast Cancer

Cancer Of Breast

BC

Breast Cancer Familial

Breast Cancer Familial Male

Breast Cancer, Familial Male

Breast Male Carcinoma

Breast Neoplasms

Breast Neoplasms, Male

Mammary Tumors

Mammary Carcinomas

Cancer, Breast

Cancer, Breast, Susceptibility

Invasive Breast Ductal Carcinoma

Breast Neoplasm

Susceptibility To Breast Cancer

Mammary Neoplasms

Animal Mammary Neoplasms

Primary Malignant Neoplasm Of Breast

Infiltrating Ductal Carcinoma Of Breast

Infiltrating Duct Carcinoma Of Unspecified Site

Infiltrating Ductular Carcinoma Of Unspecified Site

Invasive Breast Carcinoma Of No Special Type

Microinvasive Carcinoma Of Breast

Carcinoma With Apocrine Differentiation

Purulent Acute Otitis Media

Acute Suppurative Otitis Media

Acute Or Subacute Suppurative Otitis Media

Acute Or Subacute Purulent Otitis Media

Rasopathy

Ras/Mitogen-Activated Protein Kinase Syndrome

Scoliosis, Isolated 1

Adolescent Idiopathic Scoliosis

Scoliosis, Isolated, Susceptibility To, 1

Ais

IS1

Adolescent Isolated Scoliosis

Scoliosis, Idiopathic 1

Late Onset Idiopathic Scoliosis

Idiopathic Adolescent Scoliosis

Scoliosis, Idiopathic, Susceptibility To, Type 1

Smith-Magenis Syndrome

SMS

Chromosome 17p11.2 Deletion Syndrome

17p11.2 Microdeletion Syndrome

17p11.2 Monosomy

Chromosome 17p Deletion Syndrome

Del(17)

P11.2

17p- Syndrome

Deletion 17p Syndrome

Partial Monosomy 17p

Neuropathy, Hereditary Sensory And Autonomic, Type Iia

Hereditary Sensory And Autonomic Neuropathy Type 2

Hsan2

HSAN2A

Morvan Disease

Hereditary Sensory And Autonomic Neuropathy Type Ii

Neurogenic Acroosteolysis

Hsan Iia

Hsn2a

Hsn Iia

Neuropathy, Progressive Sensory, Of Children

Neuropathy, Congenital Sensory

Neuropathy, Hereditary Sensory And Autonomic, Type Ii

Hereditary Sensory And Autonomic Neuropathy Type 2a

Hereditary Sensory And Autonomic Neuropathy Type Iia

Hsanii

Congenital Sensory Neuropathy

Hsan Type Ii

Morvan Syndrome

Neuropathy, Hereditary Sensory And Autonomic, Type 2a

Neuropathy, Hereditary Sensory, Type Iia

Acroosteolysis, Neurogenic

Acroosteolysis, Giaccai Type

Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive

Hereditary Sensory Autonomic Neuropathy Type 2

Giaccai Type Acroosteolysis

Hereditary Sensory Neuropathy Type 2

Hereditary Sensory Radicular Neuropathy, Recessive Form

Hsan2b

Hsan2c

Hsan2d

Hsn Type Ii

Autosomal Recessive Sensory Radicular Neuropathy

Limbic Encephalitis-Neuromyotonia-Hyperhidrosis-Polyneuropathy Syndrome

Morvan Fibrillary Chorea

Neuropathy, Hereditary Sensory And Autonomic, 2a

Acroosteolysis Giaccai Type

Hereditary Sensory Neuropathy Type Iia

Hereditary Sensory Radicular Neuropathy Autosomal Recessive

Progressive Sensory Neuropathy Of Children

Neuropathy Congenital Sensory

Charcot-Marie-Tooth Disease

Neuropathy, Sensory And Autonomic, Hereditary, Type Iia

Morvan'S Disease

Hereditary Sensory Autonomic Neuropathy, Type 2

Hereditary Motor And Sensory-Neuropathy Type Ii

Sensory Neuropathy, Hereditary

Neuropathy, Hereditary Sensory And Autonomic, Type Iib

Autism Spectrum Disorder

Asd

Autism Spectrum Disorders

Autistic Continuum

Pervasive Developmental Disorder

Pervasive Development Disorder

Autistic Behavior

Autistic Disorder

Autistic

Autistic Disorder Of Childhood Onset

Infantile Autism

Childhood Autism

Kanner Syndrome

Pervasive Developmental Delay Nos

Pervasive Developmental Disorder, Not Otherwise Specified

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 MAPK7 VGNC VGNC:68171
Bos taurus MAPK7 VGNC VGNC:31222
Mus musculus MAPK7 MGD MGI:1346347
Rattus norvegicus MAPK7 RGD RGD:621505
Canis familiaris MAPK7 VGNC VGNC:43000
Macaca mulatta MAPK7 VGNC VGNC:74648
Others MAPK7 NCBI