1. Gene
  2. GNL3 - G protein nucleolar 3 Gene

GNL3 - G protein nucleolar 3 Gene

中文名称:G 蛋白核仁 3

种属: Homo sapiens

同用名: NS; E2IG3; NNP47; C77032

基因 ID: 26354 | 基因类型: protein coding

关于 GNL3

Cytogenetic location: 3p21.1 Genomic coordinates (GRCh38): 3:52,685,920-52,694,497 (from NCBI)

This gene has 12 transcripts (splice variants), 203 orthologues and 6 paralogues. Ubiquitous expression in urinary bladder (RPKM 35.8), prostate (RPKM 32.9) and 25 other tissues.

功能概要

该基因编码的蛋白质可能与 p53 相互作用,并可能参与肿瘤发生。编码的蛋白质似乎对干细胞增殖也很重要。这种蛋白质存在于细胞核和核仁中。已发现该基因编码两种不同亚型的三种转录变体。[RefSeq 提供,2010 年 11 月]

The protein encoded by this gene may interact with p53 and may be involved in tumorigenesis. The encoded protein also appears to be important for stem cell proliferation. This protein is found in both the nucleus and nucleolus. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]

GNL3 基因产物(3)

mRNA Protein Name
NM_014366.5 NP_055181.3 guanine nucleotide-binding protein-like 3 isoform 1
NM_206825.2 NP_996561.1 guanine nucleotide-binding protein-like 3 isoform 2
NM_206826.1 NP_996562.1 guanine nucleotide-binding protein-like 3 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 mRNA 5'-UTR binding IDA
IDA: 通过直接分析推断
16213212 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16097049 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in positive regulation of miRNA transcription IMP
IMP: 通过突变表型推断
25569094 GOA
involved in positive regulation of protein localization to chromosome, telomeric region IMP
IMP: 通过突变表型推断
22641345 GOA
involved in positive regulation of protein sumoylation IMP
IMP: 通过突变表型推断
22641345 GOA
involved in positive regulation of telomere maintenance IMP
IMP: 通过突变表型推断
22641345 GOA
involved in stem cell division IDA
IDA: 通过直接分析推断
25522312 GOA
involved in stem cell population maintenance IMP
IMP: 通过突变表型推断
25522312 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in nucleolus IDA
IDA: 通过直接分析推断
22641345 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

GNL3 蛋白结构

GN3L_Grn1

GN3L_Grn1: GNL3L/Grn1 putative GTPase (16 - 91)

MMR_HSR1

MMR_HSR1: 50S ribosome-binding GTPase (256 - 314)

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

guanine nucleotide-binding protein-like 3

E2-induced gene 3 protein

GNL3 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
GNL3 Q9BVP2 TERT Homo sapiens O14746
IF
24550003
种属内
GNL3 Q9BVP2 AGO2 Homo sapiens Q9UKV8
Anti Tag CoIP
24550003
种属内
GNL3 Q9BVP2 PPP2R5A Homo sapiens Q15172
Y2H
16097049
种属内
GNL3 Q9BVP2 CEP19 Homo sapiens Q96LK0
Y2H Array
32296183
种属内
GNL3 Q9BVP2 CEP19 Homo sapiens Q96LK0
Y2H Prey Pooling
32296183
种属内
GNL3 Q9BVP2 NLE1 Homo sapiens Q9NVX2
Anti Tag CoIP
33961781
种属间: 跨种属相互作用 种属内: 同种属相互作用

GNL3 抗体

目录号 产品名 应用 反应物种
HY-P82173 Nucleostemin Antibody (YA1918) WB, ICC/IF, FC Human

关联疾病

疾病名称 别名
Tibial Adamantinoma

Tibial Adamantinoma Morphology

Diamond-Blackfan Anemia

Congenital Pure Red Cell Aplasia

Aase Syndrome

Erythrogenesis Imperfecta

Anemia, Diamond-Blackfan

Congenital Hypoplastic Anemia

Aase-Smith Ii Syndrome

Bds

Blackfan-Diamond Anemia

Congenital Prca

Congenital Hypoplastic Anemia, Blackfan-Diamond Type

Dba

Blackfan - Diamond Syndrome

Chronic Constitutional Pure Red Cell Anaemia

Anemia Diamond Blackfan Type

Anemia Congenital Erythroid Hypoplastic

Aregenerative Anemia Chronic Congenital

Blackfan Diamond Syndrome

Red Cell Aplasia, Pure Hereditary

Aase-Smith Syndrome Ii

Bda

Blackfan Diamond Anemia

Blackfan-Diamond Disease

Blackfan-Diamond Syndrome

Chronic Congenital Agenerative Anemia

Congenital Erythroid Hypoplastic Anemia

Congenital Hypoplastic Anemia Of Blackfan And Diamond

Congenital Pure Red Cell Anemia

Hypoplastic Congenital Anemia

Inherited Erythroblastopenia

Pure Hereditary Red Cell Aplasia

Anemia, Hypoplastic, Congenital

Anemia Hypoplastic Congenital

Fanconi Anemia

Constitutional Aplastic Anemia

Diamond-Blackfan Anemia 1

Aase Smith Syndrome 2

Congenital Red Cell Aplasia

Red Cell Aplasia Of Infants

Pure Red Cell Aplasia Of Infants

Congenital Red Cell Aplastic Anaemia

Congenital Pure Red Cell Anaemia

Congenital Erythroid Hypoplasia

Pearson Marrow-Pancreas Syndrome

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 GNL3 VGNC VGNC:73038
Canis familiaris GNL3 VGNC VGNC:41327
Rattus norvegicus GNL3 RGD RGD:631354
Felis catus GNL3 VGNC VGNC:62626
Bos taurus GNL3 VGNC VGNC:29473
Mus musculus GNL3 MGD MGI:1353651