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  2. TELO2 - telomere maintenance 2 Gene

TELO2 - telomere maintenance 2 Gene

中文名称:端粒维护 2

种属: Homo sapiens

同用名: CLK2; TEL2; YHFS

基因 ID: 9894 | 基因类型: protein coding

关于 TELO2

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:1,493,360-1,510,454 (from NCBI)

This gene has 8 transcripts (splice variants), 192 orthologues and is associated with 3 phenotypes. Ubiquitous expression in spleen (RPKM 8.3), skin (RPKM 6.3) and 25 other tissues.

功能概要

该基因编码的蛋白质在细胞周期中起着 S 期检查点蛋白的作用。该蛋白质还可能在 DNA 修复中发挥作用。[RefSeq 提供,2009 年 3 月]

This gene encodes a protein that functions as an S-phase checkpoint protein in the cell cycle. The protein may also play a role in DNA repair.[provided by RefSeq, Mar 2009]

TELO2 基因产物(2)

mRNA Protein Name
NM_001351846.2 NP_001338775.1 telomere length regulation protein TEL2 homolog
NM_016111.4 NP_057195.2 telomere length regulation protein TEL2 homolog
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 Hsp90 protein binding IPI
IPI: 通过物理相互作用推断
20864032 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
18160036 GOA
enables protein kinase binding IPI
IPI: 通过物理相互作用推断
20864032 GOA
enables protein-containing complex binding IDA
IDA: 通过直接分析推断
20864032 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in protein stabilization IMP
IMP: 通过突变表型推断
24036451 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of TTT Hsp90 cochaperone complex IPI
IPI: 通过物理相互作用推断
20810650 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
20864032 GOA
located in nucleus IDA
IDA: 通过直接分析推断
20864032 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

TELO2 蛋白结构

Telomere_reg-2

Telomere_reg-2: Telomere length regulation protein (512 - 620)

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

telomere length regulation protein TEL2 homolog

TEL2, telomere maintenance 2, homolog

TELO2 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
TELO2 Q9Y4R8 TTI1 Homo sapiens O43156
GMS
20810650
种属内
TELO2 Q9Y4R8 TTI1 Homo sapiens O43156
TAP
20801936
种属内
TELO2 Q9Y4R8 TTI1 Homo sapiens O43156 20810650
种属内
TELO2 Q9Y4R8 PIH1D1 Homo sapiens Q9NWS0 24656813
种属内
TELO2 Q9Y4R8 PIH1D1 Homo sapiens Q9NWS0 24656813
种属内
TELO2 Q9Y4R8 PIH1D1 Homo sapiens Q9NWS0 24656813
种属内
TELO2 Q9Y4R8 PIH1D1 Homo sapiens Q9NWS0
ITC
24656813
种属内
TELO2 Q9Y4R8 ATM Homo sapiens Q13315
TAP
20801936
种属内
TELO2 Q9Y4R8 ATM Homo sapiens Q13315 18160036
种属内
TELO2 Q9Y4R8 ATM Homo sapiens Q13315 18160036
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
You-Hoover-Fong Syndrome

Telo2-Related Intellectual Disability-Neurodevelopmental Disorder

YHFS

Nail-Patella Syndrome

Turner-Kieser Syndrome

Onychoosteodysplasia

Fong Disease

NPS

Hereditary Onycho-Osteodysplasia

Nps1

Hereditary Onychoostedysplasia

Iliac Horn Syndrome

Nail Patella Syndrome

Turner-Kiser Syndrome

Arthro-Onychodysplasia

Nps 1

Osteo-Onychodysplasia

Hereditary Osteo-Onychodysplasia

Osterreicher Syndrome

Pelvic Horn Syndrome

Österreicher-Turner Syndrome

Nps - [Nail-Patella Syndrome]

Hood - [Hereditary Onycho-Osteodysplasia] Syndrome

Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly

Seckel Syndrome

Microcephalic Primordial Dwarfism

Bird-Headed Dwarfism

Harper'S Syndrome

Virchow-Seckel Dwarfism

Nanocephalic Dwarfism

Sckl

Seckel-Type Dwarfism

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 TELO2 VGNC VGNC:35740
Mus musculus TELO2 MGD MGI:1918968
Felis catus TELO2 VGNC VGNC:66069
Rattus norvegicus TELO2 RGD RGD:1305553
Canis familiaris TELO2 VGNC VGNC:47245
Macaca mulatta TELO2 VGNC VGNC:99609