1. Gene
  2. MARK4 - microtubule affinity regulating kinase 4 Gene

MARK4 - microtubule affinity regulating kinase 4 Gene

中文名称:微管亲和力调节激酶 4

种属: Homo sapiens

同用名: MARK4L; MARK4S; MARKL1; PAR-1D; MARKL1L

基因 ID: 57787 | 基因类型: protein coding

关于 MARK4

Cytogenetic location: 19q13.32 Genomic coordinates (GRCh38): 19:45,251,271-45,305,284 (from NCBI)

This gene has 9 transcripts (splice variants), 270 orthologues and 3 paralogues. Broad expression in testis (RPKM 14.0), brain (RPKM 8.1) and 25 other tissues.

功能概要

该基因编码微管亲和力调节激酶家族的成员。这些蛋白激酶磷酸化微管相关蛋白并调节稳定和动态微管之间的转换。编码的蛋白质在整个有丝分裂过程中与中心体相关,并可能参与细胞周期控制。该基因的表达是癌症的潜在标志物,编码的蛋白质也可能在阿尔茨海默病中发挥作用。该基因的假基因位于 3 号染色体的短臂和长臂上。已经观察到该基因编码多种亚型的选择性剪接转录物变体。[RefSeq 提供,2010 年 12 月]

This gene encodes a member of the microtubule affinity-regulating kinase family. These protein kinases phosphorylate microtubule-associated proteins and regulate the transition between stable and dynamic microtubules. The encoded protein is associated with the centrosome throughout mitosis and may be involved in cell cycle control. Expression of this gene is a potential marker for Cancer, and the encoded protein may also play a role in Alzheimer's disease. Pseudogenes of this gene are located on both the short and long arm of chromosome 3. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]

MARK4 基因产物(2)

mRNA Protein Name
NM_001199867.2 NP_001186796.1 MAP/microtubule affinity-regulating kinase 4 isoform 1
NM_031417.4 NP_113605.2 MAP/microtubule affinity-regulating kinase 4 isoform 2
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 cytoskeletal anchor activity IDA
IDA: 通过直接分析推断
28656979 GOA
enables gamma-tubulin binding IDA
IDA: 通过直接分析推断
14594945 GOA
enables microtubule binding IDA
IDA: 通过直接分析推断
14594945 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
14594945 GOA
enables tau-protein kinase activity IDA
IDA: 通过直接分析推断
14594945 GOA
enables tau-protein kinase activity IMP
IMP: 通过突变表型推断
23666762 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cilium organization IGI
IGI: 通过遗传相互作用推断
23400999 GOA
involved in microtubule bundle formation IEP
IEP: 通过表达模式推断
14594945 GOA
NOT involved in microtubule cytoskeleton organization IMP
IMP: 通过突变表型推断
23400999 GOA
involved in microtubule cytoskeleton organization IMP
IMP: 通过突变表型推断
14594945 GOA
involved in nervous system development IDA
IDA: 通过直接分析推断
14594945 GOA
involved in positive regulation of NLRP3 inflammasome complex assembly IDA
IDA: 通过直接分析推断
28656979 GOA
acts upstream of or within positive regulation of cell cycle IDA
IDA: 通过直接分析推断
26882547 GOA
involved in positive regulation of cilium assembly IMP
IMP: 通过突变表型推断
23400999 GOA
involved in positive regulation of protein localization to centrosome IMP
IMP: 通过突变表型推断
23400999 GOA
involved in protein phosphorylation IMP
IMP: 通过突变表型推断
23666762 GOA
involved in regulation of centrosome cycle IMP
IMP: 通过突变表型推断
25123532 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in centrosome IDA
IDA: 通过直接分析推断
14594945 GOA
located in ciliary basal body IMP
IMP: 通过突变表型推断
23400999 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
23666762 GOA
located in dendrite IDA
IDA: 通过直接分析推断
23666762 GOA
part of gamma-tubulin complex IDA
IDA: 通过直接分析推断
25123532 GOA
located in microtubule cytoskeleton IDA
IDA: 通过直接分析推断
14594945 GOA
is active in microtubule organizing center IDA
IDA: 通过直接分析推断
28656979 GOA
located in microtubule organizing center IDA
IDA: 通过直接分析推断
14594945 GOA
located in midbody IDA
IDA: 通过直接分析推断
25123532 GOA
located in neuron projection IDA
IDA: 通过直接分析推断
14594945 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

MARK4 蛋白结构

Pkinase

Pkinase: Protein kinase domain (59 - 310)

UBA

UBA: UBA/TS-N domain (332 - 366)

KA1

KA1: Kinase associated domain 1 (708 - 752)

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

MAP/microtubule affinity-regulating kinase 4

MAP/microtubule affinity-regulating kinase like 1

MARK4 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 MARK4 Q96L34 PRKCI Homo sapiens P41743
Anti Tag CoIP
14676191
Intra MARK4 Q96L34 PARD6G Homo sapiens Q9BYG4
Anti Tag CoIP
14676191
Intra MARK4 Q96L34 PNMA1 Homo sapiens Q8ND90
Anti Tag CoIP
14676191
Intra MARK4 Q96L34 TUBG1 Homo sapiens P23258
Anti Tag CoIP
14676191
Intra MARK4 Q96L34 TUBG1 Homo sapiens P23258
Anti Tag CoIP
14594945
Intra MARK4 Q96L34 TUBG1 Homo sapiens P23258
TAP
14594945
Intra MARK4 Q96L34 STK11 Homo sapiens Q15831
Anti Tag CoIP
14676191
Intra MARK4 Q96L34 YWHAH Homo sapiens Q04917
Anti Tag CoIP
14676191
Intra MARK4 Q96L34 YWHAH Homo sapiens Q04917
Anti Tag CoIP
16959763
Intra MARK4 Q96L34 LYN Homo sapiens P07948
Validated Y2H
32814053
Intra MARK4 Q96L34 LYN Homo sapiens P07948
Y2H Array
32814053
Intra MARK4 Q96L34 LYN Homo sapiens P07948
Y2H Pooling
32814053
Intra MARK4 Q96L34 CDC42 Homo sapiens P60953
Anti Tag CoIP
14676191
Intra MARK4 Q96L34 KRT31 Homo sapiens Q15323
Y2H Prey Pooling
25416956
Intra MARK4 Q96L34 KRT31 Homo sapiens Q15323
Y2H Array
25416956
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
Peutz-Jeghers Syndrome

PJS

Polyposis, Hamartomatous Intestinal

Polyps-And-Spots Syndrome

Lentiginosis, Perioral

Periorificial Lentiginosis Syndrome

Hamartomatous Intestinal Polyposis

Hamartomatous Polyp

Colonic Hamartomatous Polyp

Gastric Peutz-Jeghers Polyp

Peutz Jeghers Colon Polyp

Peutz Jeghers Polyp

Peutz-Jeghers Polyp Of Small Intestine

Peutz-Jeghers Small Bowel Hamartoma

Peutz Jeghers Polyposis

Intestinal Polyposis-Cutaneous Pigmentation Syndrome

Peutz-Jeghers Polyposis

Polyposis, Intestinal, Ii

Intestinal Hamartomatous Polyposis

Peutz-Jeghers Polyp

Peutz-Jeghers Polyp Of The Stomach

Peutz Jehgers Polyp

Peutz-Jeghers Polyps Of Small Bowel

Parkinson Disease 6, Autosomal Recessive Early-Onset

Autosomal Recessive Early-Onset Parkinson Disease 6

Parkinson Disease 6

PARK6

Parkinson Disease 6, Early Onset

Parkinson'S Disease 6

Parkinson Disease 6, Early-Onset

Autosomal Recessive Early-Onset Parkinson'S Disease 6

Early-Onset Parkinson Disease 6

Autosomal Recessive Early-Onset Parkinson Disease Type 6

Parkinson Disease 6 Early-Onset

Parkinson Disease 6 Late-Onset Susceptibility To

Parkinson Disease Autosomal Recessive Early-Onset Digenic Pink1/Dj1

Parkinsonism Young Adult Onset

Parkinson Disease, Autosomal Recessive Early-Onset, Digenic, Pink1/Dj1

Parkinson Disease, Type 6, Autosomal Recessive, Early-Onset

Alzheimer'S Disease 1

Alzheimer Disease Type 1

Alzheimer'S Disease 1, Early Onset

Hermansky-Pudlak Syndrome 1

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

HPS1

Delta Storage Pool Disease

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial

Hermansky-Pudlak Syndrome, Type 1

Platelet Storage Pool Deficiency

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
Macaca mulatta MARK4 VGNC VGNC:74508
Bos taurus MARK4 VGNC VGNC:52203
Mus musculus MARK4 MGD MGI:1920955
Canis familiaris MARK4 VGNC VGNC:43026
Rattus norvegicus MARK4 RGD RGD:1591792
Felis catus MARK4 VGNC VGNC:63390
Others MARK4 NCBI