1. Gene
  2. TNPO2 - transportin 2 Gene

TNPO2 - transportin 2 Gene

中文名称:转运 2

种属: Homo sapiens

同用名: IPO3; TRN2; KPNB2B; IDDHISD

基因 ID: 30000 | 基因类型: protein coding

关于 TNPO2

Cytogenetic location: 19p13.13 Genomic coordinates (GRCh38): 19:12,699,201-12,723,932 (from NCBI)

This gene has 18 transcripts (splice variants), 189 orthologues, 5 paralogues and is associated with 2 phenotypes. Ubiquitous expression in brain (RPKM 25.6), testis (RPKM 20.6) and 25 other tissues.

功能概要

预测启用核输入信号受体活性和核定位序列结合活性。预计参与蛋白质输入细胞核。预计在肌肉细胞分化的负调节上游或负调节内起作用。预计在细胞质和细胞核中有活性。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to enable nuclear import signal receptor activity and nuclear localization sequence binding activity. Predicted to be involved in protein import into nucleus. Predicted to act upstream of or within negative regulation of muscle cell differentiation. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2022]

TNPO2 基因产物(11)

mRNA Protein Name
NM_001136195.2 NP_001129667.1 transportin-2 isoform 2
NM_001136196.2 NP_001129668.1 transportin-2 isoform 1
NM_001382236.1 NP_001369165.1 transportin-2 isoform 2
NM_001382237.1 NP_001369166.1 transportin-2 isoform 2
NM_001382238.1 NP_001369167.1 transportin-2 isoform 2
NM_001382239.1 NP_001369168.1 transportin-2 isoform 2
NM_001382240.1 NP_001369169.1 transportin-2 isoform 1
NM_001382241.1 NP_001369170.1 transportin-2 isoform 1
NM_001382242.1 NP_001369171.1 transportin-2 isoform 1
NM_001382243.1 NP_001369172.1 transportin-2 isoform 3
NM_013433.5 NP_038461.2 transportin-2 isoform 2
基因本体论
  • 分子功能
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
12896982 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

TNPO2 蛋白结构

IBN_N

IBN_N: Importin-beta N-terminal domain (32 - 98)

HEAT_EZ

HEAT_EZ: HEAT-like repeat (408 - 461)

HEAT

HEAT: HEAT repeat (665 - 695)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 897 a.a.
蛋白主名 其他名称

transportin-2

importin 3

TNPO2 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
TNPO2 O14787 PNMA5 Homo sapiens Q96PV4
Y2H Prey Pooling
25416956
种属内
TNPO2 O14787 CAMK2D Homo sapiens Q13557
Y2H Prey Pooling
25416956
种属内
TNPO2 O14787 CAMK2D Homo sapiens Q13557
Y2H Array
31515488
种属内
TNPO2 O14787 APIP Homo sapiens Q96GX9
Y2H Array
25416956
种属内
TNPO2 O14787 APIP Homo sapiens Q96GX9
Y2H Array
31515488
种属内
TNPO2 O14787 APIP Homo sapiens Q96GX9
Validated Y2H
25416956
种属内
TNPO2 O14787 TERF1 Homo sapiens P54274
Pull Down
21044950
种属内
TNPO2 O14787 NME1 Homo sapiens P15531
Validated Y2H
25416956
种属内
TNPO2 O14787 NME1 Homo sapiens P15531
Y2H Prey Pooling
25416956
种属内
TNPO2 O14787 KLHL2 Homo sapiens O95198
Y2H Array
31515488
种属内
TNPO2 O14787 KLHL2 Homo sapiens O95198
Y2H Prey Pooling
25416956
种属内
TNPO2 O14787 KLHL2 Homo sapiens O95198
Validated Y2H
25416956
种属内
TNPO2 O14787 KLHL2 Homo sapiens O95198
Y2H Array
25416956
种属内
TNPO2 O14787 C1orf94 Homo sapiens Q6P1W5
Y2H Prey Pooling
25416956
种属内
TNPO2 O14787 C1orf94 Homo sapiens Q6P1W5
Y2H Array
25416956
种属内
TNPO2 O14787 EXOC5 Homo sapiens O00471
Y2H Prey Pooling
25416956
种属内
TNPO2 O14787 EXOC5 Homo sapiens O00471
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
Intellectual Developmental Disorder With Hypotonia, Impaired Speech, And Dysmorphic Facies

IDDHISD

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 TNPO2 VGNC VGNC:79216
Canis familiaris TNPO2 VGNC VGNC:47695
Rattus norvegicus TNPO2 RGD RGD:1310356
Felis catus TNPO2 VGNC VGNC:66431
Mus musculus TNPO2 MGD MGI:2384849
Bos taurus TNPO2 VGNC VGNC:36200