1. Gene
  2. CETN1 - centrin 1 Gene

CETN1 - centrin 1 Gene

中文名称:中心素 1

种属: Homo sapiens

同用名: CEN1; CETN

基因 ID: 1068 | 基因类型: protein coding

关于 CETN1

Cytogenetic location: 18p11.32 Genomic coordinates (GRCh38): 18:580,380-582,114 (from NCBI)

This gene has 1 transcript (splice variant), 206 orthologues and 20 paralogues.

功能概要

该基因编码的蛋白质在决定中心体位置和分离以及微管切断过程中起着重要作用。该蛋白定位于间期细胞的中心体,并在有丝分裂期间重新分布到纺锤体两极区域,反映了细胞周期中中心体的动态行为。[RefSeq 提供,2015 年 1 月]

The protein encoded by this gene plays important roles in the determination of centrosome position and segregation, and in the process of microtubule severing. This protein is localized to the centrosome of interphase cells, and redistributes to the region of the spindle poles during mitosis, reflecting the dynamic behavior of the centrosome during the cell cycle. [provided by RefSeq, Jan 2015]

CETN1 基因产物(1)

mRNA Protein Name
NM_004066.3 NP_004057.1 centrin-1
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
20643351 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in centriole IDA
IDA: 通过直接分析推断
18331714 GOA
located in centrosome IDA
IDA: 通过直接分析推断
8175926 GOA
located in centrosome IMP
IMP: 通过突变表型推断
18331714 GOA
located in spindle pole IDA
IDA: 通过直接分析推断
8175926 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

CETN1 蛋白结构

EF-hand_7

EF-hand_7: EF-hand domain pair (33 - 93)

EF-hand_8

EF-hand_8: EF-hand domain pair (117 - 167)

  • 0
  • 100
  • 172 a.a.
蛋白主名 其他名称

centrin-1

EF-hand protein

CETN1 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 CETN1 Q12798 SGSM1 Homo sapiens Q2NKQ1-4
Anti Tag CoIP
28514442
Intra CETN1 Q12798 SGSM1 Homo sapiens Q2NKQ1-4
Y2H Array
32296183
Intra CETN1 Q12798 SGSM1 Homo sapiens Q2NKQ1-4
Validated Y2H
25416956
Intra CETN1 Q12798 SGSM1 Homo sapiens Q2NKQ1-4
Validated Y2H
32296183
Intra CETN1 Q12798 SGSM1 Homo sapiens Q2NKQ1-4
Y2H Prey Pooling
25416956
Intra CETN1 Q12798 SGSM1 Homo sapiens Q2NKQ1-4
Y2H Prey Pooling
32296183
Intra CETN1 Q12798 SGSM1 Homo sapiens Q2NKQ1
Anti Tag CoIP
33961781
Intra CETN1 Q12798 POC5 Homo sapiens Q8NA72-3
Validated Y2H
32296183
Intra CETN1 Q12798 POC5 Homo sapiens Q8NA72-3
Anti Tag CoIP
28514442
Intra CETN1 Q12798 POC5 Homo sapiens Q8NA72
Y2H Array
31515488
Intra CETN1 Q12798 POC5 Homo sapiens Q8NA72
Anti Tag CoIP
33961781
Intra CETN1 Q12798 POC5 Homo sapiens Q8NA72
Validated Y2H
25416956
Intra CETN1 Q12798 POC5 Homo sapiens Q8NA72
Y2H Prey Pooling
25416956
Intra CETN1 Q12798 POC5 Homo sapiens Q8NA72
Y2H Array
25416956
Intra CETN1 Q12798 POC5 Homo sapiens Q8NA72
Y2H Array
29892012
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
Autosomal Dominant Intellectual Developmental Disorder 40

Autosomal Dominant Non-Syndromic Intellectual Disability 40

Autosomal Dominant Mental Retardation 40

Mrd40

Mental Retardation, Autosomal Dominant 40

Night Blindness, Congenital Stationary, Autosomal Dominant 2

Congenital Stationary Night Blindness Autosomal Dominant 2

CSNBAD2

Hemeralopia

Night Blindness, Congenital Stationary, Rambusch Type

Rambusch Type Congenital Stationary Night Blindness

Congenital Stationary Night Blindness Rambusch Type

Hemeralopia Congenital Essential

Blindness, Night, Stationary, Congenital, Autosomal Dominant, Type 2

Primary Autosomal Recessive Microcephaly

Autosomal Recessive Primary Microcephaly

Mcph

True Microcephaly

Microcephalia Vera

Microcephaly Vera

Microcephaly Primary Hereditary

Microcephaly, Primary, Autosomal Recessive

Primary Microcephaly

Primary Ciliary Dyskinesia

Immotile Cilia Syndrome

Kartagener Syndrome

Dextrocardia Bronchiectasis And Sinusitis

Pcd

Ciliary Motility Disorders

Ciliary Motility Disorder

Immotile Ciliary Syndrome

Ciliary Dyskinesia Primary

Ics

Polynesian Bronchiectasis

Dextrocardia-Bronchiectasis-Sinusitis Syndrome

Immotile Cilia Syndrome, Kartagener Type

Primary Ciliary Dyskinesia And Situs Inversus

Primary Ciliary Dyskinesia, Kartagener Type

Siewert Syndrome

Dyskinesia, Ciliary, Primary

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

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 CETN1 MGD MGI:1347086
Macaca mulatta CETN1 VGNC VGNC:71013
Rattus norvegicus CETN1 RGD RGD:620246
Felis catus CETN1 VGNC VGNC:60799
Canis familiaris CETN1 VGNC VGNC:39155
Bos taurus CETN1 VGNC VGNC:27233