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  2. CDT1 - chromatin licensing and DNA replication factor 1 Gene

CDT1 - chromatin licensing and DNA replication factor 1 Gene

中文名称:染色质许可和 DNA 复制因子 1

种属: Homo sapiens

同用名: DUP; RIS2

基因 ID: 81620 | 基因类型: protein coding

关于 CDT1

Cytogenetic location: 16q24.3 Genomic coordinates (GRCh38): 16:88,803,789-88,809,258 (from NCBI)

This gene has 3 transcripts (splice variants), 203 orthologues and is associated with 3 phenotypes. Biased expression in bone marrow (RPKM 13.5), placenta (RPKM 2.5) and 9 other tissues.

功能概要

该基因编码的蛋白质参与了 DNA 复制所必需的复制前复合物的形成。编码的蛋白质可以结合孪蛋白,从而防止复制,并可能起到防止这种蛋白质在不适当的起点开始复制的作用。细胞周期蛋白 A 依赖性激酶对该蛋白质的磷酸化导致蛋白质降解。[RefSeq 提供,2011 年 3 月]

The protein encoded by this gene is involved in the formation of the pre-replication complex that is necessary for DNA replication. The encoded protein can bind geminin, which prevents replication and may function to prevent this protein from initiating replication at inappropriate origins. Phosphorylation of this protein by cyclin A-dependent kinases results in degradation of the protein. [provided by RefSeq, Mar 2011]

CDT1 基因产物(1)

mRNA Protein Name
NM_030928.4 NP_112190.2 DNA replication factor Cdt1
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 chromatin binding IDA
IDA: 通过直接分析推断
11125146 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
11125146 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in kinetochore IDA
IDA: 通过直接分析推断
22581055 GOA
located in nucleus IDA
IDA: 通过直接分析推断
11125146 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

CDT1 蛋白结构

CDT1

CDT1: DNA replication factor CDT1 like (186 - 350)

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

DNA replication factor Cdt1

Double parked, Drosophila, homolog of

CDT1 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
种属内
CDT1 Q9H211 PCNA Homo sapiens P12004
Pull Down
16482215
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
Peptide Array
15232106
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
Pull Down
11125146
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
BFG-2H
27107012
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
Pull Down
19906994
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
CoIP
11125146
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
Pull Down
16482215
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
X-Ray Diffraction
19906994
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
SAXS
19906994
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
Y2H
22581055
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
GMS
19906994
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
Anti Tag CoIP
21543332
种属内
CDT1 Q9H211 GMNN Homo sapiens O75496
SPR
19906994
种属内
CDT1 Q9H211 CDC6 Homo sapiens Q99741
Pull Down
14672932
种属内
CDT1 Q9H211 MCM6 Homo sapiens Q14566
Anti Tag CoIP
26496610
种属内
CDT1 Q9H211 MCM6 Homo sapiens Q14566
NMR
20202939
种属内
CDT1 Q9H211 NDC80 Homo sapiens O14777
Pull Down
22581055
种属内
CDT1 Q9H211 NDC80 Homo sapiens O14777
Anti Bait CoIP
22581055
种属内
CDT1 Q9H211 NDC80 Homo sapiens O14777
Y2H
22581055
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
Meier-Gorlin Syndrome 4

MGORS4

Meier-Gorlin Syndrome, Type 4

Meier-Gorlin Syndrome 1

Meier-Gorlin Syndrome

Ear, Patella, Short Stature Syndrome

Microtia, Absent Patellae, Micrognathia Syndrome

MGORS1

Eps

Ear-Patella-Short Stature Syndrome

Ear Patella Short Stature Syndrome

Microtia Absent Patellae Micrognathia Syndrome

Meier-Gorlin Syndrome, Type 1

Genitourinary Tract Anomalies
Microtia

Congenital Small Ears

Hypoplasia Of Ear

Meier-Gorlin Syndrome 7

MGORS7

Meier-Gorlin Syndrome, Type 7

Meier-Gorlin Syndrome 5

MGORS5

Meier-Gorlin Syndrome, Type 5

Isolated Growth Hormone Deficiency, Type Ia

Ighd Ia

Primordial Dwarfism

Isolated Growth Hormone Deficiency Type Ia

Sexual Ateleiotic Dwarfism

Pituitary Dwarfism I

IGHD1A

Illig-Type Growth Hormone Deficiency

Growth Hormone Deficiency, Isolated, Type Ia

Congenital Ighd Type Ia

Congenital Isolated Gh Deficiency Type Ia

Congenital Isolated Growth Hormone Deficiency Type Ia

Pituitary Dwarfism 1

Growth Hormone Deficiency, Isolated, Autosomal Recessive

Autosomal Recessive Isolated Growth Hormone Deficiency

Isolated Growth Hormone Deficiency Type 1a

Congenital Ighd

Congenital Isolated Gh Deficiency

Congenital Isolated Growth Hormone Deficiency

Growth Hormone Deficiency, Isolated Autosomal Recessive

Illig Type Growth Hormone Deficiency

Non-Acquired Isolated Growth Hormone Deficiency

Growth Hormone Deficiency, Isolated, 1a

Growth Hormone Deficiency Isolated Autosomal Recessive

Dwarfism, Primordial

Dwarfism

Seckel Syndrome

Microcephalic Primordial Dwarfism

Bird-Headed Dwarfism

Harper'S Syndrome

Virchow-Seckel Dwarfism

Nanocephalic Dwarfism

Sckl

Seckel-Type Dwarfism

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
Bos taurus CDT1 VGNC VGNC:27158
Canis familiaris CDT1 VGNC VGNC:39083
Macaca mulatta CDT1 VGNC VGNC:71092
Felis catus CDT1 VGNC VGNC:60721
Rattus norvegicus CDT1 RGD RGD:1309211
Mus musculus CDT1 MGD MGI:1914427