1. Gene
  2. IPO8 - importin 8 Gene

IPO8 - importin 8 Gene

中文名称:导入 8

种属: Homo sapiens

同用名: VISS; RANBP8

基因 ID: 10526 | 基因类型: protein coding

关于 IPO8

Cytogenetic location: 12p11.21 Genomic coordinates (GRCh38): 12:30,628,988-30,695,869 (from NCBI)

This gene has 11 transcripts (splice variants), 202 orthologues, 4 paralogues and is associated with 2 phenotypes. Ubiquitous expression in thyroid (RPKM 11.8), testis (RPKM 10.7) and 25 other tissues.

功能概要

importin-alpha/beta 复合物和 GTPase Ran 介导具有经典核定位信号的蛋白质的核输入。由该基因编码的蛋白质是大约 20 个潜在 Ran 目标的成员,这些目标共享与 importin-beta 的 Ran 结合位点相关的序列基序。这种蛋白质与核孔复合体结合,并与 RanGTP 和 RANBP1 一起抑制 Ran GTP 酶的 GAP 刺激。已发现该基因编码不同亚型的可变剪接转录物变体。[RefSeq 提供,2010 年 7 月]

The importin-alpha/beta complex and the GTPase Ran mediate nuclear import of proteins with a classical nuclear localization signal. The protein encoded by this gene is a member of a class of approximately 20 potential Ran targets that share a sequence motif related to the Ran-binding site of importin-beta. This protein binds to the nuclear pore complex and, along with RanGTP and RANBP1, inhibits the GAP stimulation of the Ran GTPase. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]

IPO8 基因产物(2)

mRNA Protein Name
NM_001190995.2 NP_001177924.1 importin-8 isoform 2
NM_006390.4 NP_006381.2 importin-8 isoform 1
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
17785517 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

IPO8 蛋白结构

IBN_N

IBN_N: Importin-beta N-terminal domain (22 - 101)

Cse1

Cse1: Cse1 (201 - 441)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1037 a.a.
蛋白主名 其他名称

importin-8

RAN binding protein 8

IPO8 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 IPO8 O15397 ZNF774 Homo sapiens Q6NX45
Validated Y2H
32296183
Intra IPO8 O15397 ZNF331 Homo sapiens Q9NQX6
Anti Tag CoIP
26496610
Intra IPO8 O15397 AGO3 Homo sapiens Q9H9G7
Anti Tag CoIP
19167051
Intra IPO8 O15397 AGO3 Homo sapiens Q9H9G7
Confocal
19167051
Intra IPO8 O15397 AGO4 Homo sapiens Q9HCK5
Anti Tag CoIP
19167051
Intra IPO8 O15397 AGO4 Homo sapiens Q9HCK5
Pull Down
19167051
Intra IPO8 O15397 ZNF264 Homo sapiens O43296
Validated Y2H
32296183
Intra IPO8 O15397 AGO1 Homo sapiens Q9UL18
Anti Tag CoIP
19167051
Intra IPO8 O15397 AGO1 Homo sapiens Q9UL18
Pull Down
19167051
Intra IPO8 O15397 AGO2 Homo sapiens Q9UKV8
Anti Bait CoIP
19167051
Intra IPO8 O15397 AGO2 Homo sapiens Q9UKV8
Pull Down
19167051
Intra IPO8 O15397 ZFP2 Homo sapiens Q6ZN57
Validated Y2H
32296183
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
Viss Syndrome

VISS

Vascular Aneurysm, Immune Dysregulation, Skeletal Anomalies, And Skin And Joint Laxity

Aortic Aneurysm

Aortic Rupture

Thoracoabdominal Aortic Aneurysm, Ruptured

Ruptured Aortic Aneurysm

Aortic Aneurysms

Aortic Aneurysm Without Mention Of Rupture Nos

Ruptured Abdominal Aortic Aneurysm

Aortic Aneurysm, Ruptured

Ruptured Thoracic Aortic Aneurysm

Autosomal Recessive Nonsyndromic Deafness 32

Deafness, Autosomal Recessive 32

Autosomal Recessive Deafness 105

Autosomal Recessive Deafness 32

Dfnb32

Hearing Impairment Infertile Male Syndrome

Hiims

Deafness, Autosomal Recessive, Type 32

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 IPO8 VGNC VGNC:73815
Mus musculus IPO8 MGD MGI:2444611
Bos taurus IPO8 VGNC VGNC:30245
Felis catus IPO8 VGNC VGNC:69234
Canis familiaris IPO8 VGNC VGNC:42068
Rattus norvegicus IPO8 RGD RGD:1593688