1. Gene
  2. SNX15 - sorting nexin 15 Gene

SNX15 - sorting nexin 15 Gene

中文名称:分选 nexin 15

种属: Homo sapiens

同用名: HSAF001435

基因 ID: 29907 | 基因类型: protein coding

关于 SNX15

Cytogenetic location: 11q13.1 Genomic coordinates (GRCh38): 11:65,027,439-65,040,572 (from NCBI)

This gene has 7 transcripts (splice variants), 182 orthologues and 2 paralogues. Ubiquitous expression in fat (RPKM 9.4), kidney (RPKM 8.6) and 25 other tissues.

功能概要

该基因编码分选连接蛋白家族的一个成员。该家族的成员包含一个 phox (PX) 结构域,它是一个磷酸肌醇结合结构域,并参与细胞内运输。该基因的过度表达导致胰岛素和肝细胞生长因子受体对其成熟亚基的加工减少。这种减少是由弗林蛋白酶的错误定位引起的,弗林蛋白酶是负责切割胰岛素和肝细胞生长因子受体的内切蛋白酶。这种蛋白质参与从质膜到再循环核内体或跨高尔基体网络的核内体运输。可变剪接导致多个转录本变体。该基因与上游 ADP-核糖基化因子样 2 (ARL2) 基因之间也存在通读转录。[RefSeq 提供,2010 年 12 月]

This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of Insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of Furin, the endoprotease responsible for cleavage of Insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like 2 (ARL2) gene. [provided by RefSeq, Dec 2010]

SNX15 基因产物(2)

mRNA Protein Name
NM_013306.5 NP_037438.2 sorting nexin-15 isoform A
NM_147777.4 NP_680086.2 sorting nexin-15 isoform B
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
16189514 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

SNX15 蛋白结构

PX

PX: PX domain (11 - 123)

MIT

MIT: MIT (microtubule interacting and transport) domain (268 - 335)

  • 0
  • 100
  • 200
  • 300
  • 342 a.a.
蛋白主名 其他名称

sorting nexin-15

clone iota unknown protein

SNX15 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
SNX15 Q9NRS6 REEP6 Homo sapiens Q96HR9-2
Y2H Array
32296183
种属内
SNX15 Q9NRS6 REEP6 Homo sapiens Q96HR9-2
Y2H Prey Pooling
32296183
种属内
SNX15 Q9NRS6 RABAC1 Homo sapiens Q9UI14
Y2H Prey Pooling
25416956
种属内
SNX15 Q9NRS6 RABAC1 Homo sapiens Q9UI14
Y2H Array
25416956
种属内
SNX15 Q9NRS6 ARL6IP1 Homo sapiens Q15041
Y2H Prey Pooling
25416956
种属内
SNX15 Q9NRS6 ARL6IP1 Homo sapiens Q15041
Y2H Array
25416956
种属内
SNX15 Q9NRS6 RTN4 Homo sapiens Q9NQC3
Y2H Prey Pooling
25416956
种属内
SNX15 Q9NRS6 RTN4 Homo sapiens Q9NQC3
Y2H
21516116
种属内
SNX15 Q9NRS6 NT5C2 Homo sapiens P49902
Anti Tag CoIP
33961781
种属内
SNX15 Q9NRS6 NT5C2 Homo sapiens P49902
Anti Tag CoIP
28514442
种属内
SNX15 Q9NRS6 REEP6 Homo sapiens Q96HR9
Validated Y2H
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
Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia

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
Mus musculus SNX15 MGD MGI:1916274
Canis familiaris SNX15 VGNC VGNC:46624
Macaca mulatta SNX15 VGNC VGNC:107646
Rattus norvegicus SNX15 RGD RGD:1305803
Bos taurus SNX15 VGNC VGNC:35095
Felis catus SNX15 VGNC VGNC:81935