1. Gene
  2. SYS1 - SYS1 golgi trafficking protein Gene

SYS1 - SYS1 golgi trafficking protein Gene

中文名称:SYS1 高尔基体运输蛋白

种属: Homo sapiens

同用名: C20orf169; dJ453C12.4; dJ453C12.4.1

基因 ID: 90196 | 基因类型: protein coding

关于 SYS1

Cytogenetic location: 20q13.12 Genomic coordinates (GRCh38): 20:45,361,949-45,376,798 (from NCBI)

This gene has 8 transcripts (splice variants), 192 orthologues and 1 paralogue. Ubiquitous expression in thyroid (RPKM 8.9), ovary (RPKM 6.7) and 25 other tissues.

功能概要

SYS1 与 ADP 核糖基化因子相关蛋白 ARFRP1 (MIM 604699) 形成复合物并将 ARFRP1 靶向高尔基体 (Behnia 等人,2004 [PubMed 15077113]) 。[OMIM 提供,2009 年 8 月]

SYS1 forms a complex with ADP-ribosylation factor-related protein ARFRP1 (MIM 604699) and targets ARFRP1 to the Golgi apparatus (Behnia et al., 2004 [PubMed 15077113]).[supplied by OMIM, Aug 2009]

SYS1 基因产物(3)

mRNA Protein Name
NM_001099791.3 NP_001093261.1 protein SYS1 homolog isoform b
NM_001197129.2 NP_001184058.1 protein SYS1 homolog isoform a
NM_033542.4 NP_291020.1 protein SYS1 homolog isoform a
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
32296183 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

SYS1 蛋白结构

SYS1

SYS1: Integral membrane protein S linking to the trans Golgi network (5 - 148)

  • 0
  • 100
  • 156 a.a.
蛋白主名 其他名称

protein SYS1 homolog

SYS1 Golgi-localized integral membrane protein homolog

SYS1 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
SYS1 Q8N2H4 SLC30A8 Homo sapiens Q8IWU4 32296183
种属内
SYS1 Q8N2H4 SLC30A8 Homo sapiens Q8IWU4 32296183
种属内
SYS1 Q8N2H4 TMEM248 Homo sapiens Q9NWD8 32296183
种属内
SYS1 Q8N2H4 TMEM248 Homo sapiens Q9NWD8 32296183
种属内
SYS1 Q8N2H4 TMEM248 Homo sapiens Q9NWD8 32296183
种属内
SYS1 Q8N2H4 HSD17B11 Homo sapiens Q8NBQ5 32296183
种属内
SYS1 Q8N2H4 HSD17B11 Homo sapiens Q8NBQ5 32296183
种属内
SYS1 Q8N2H4 HSD17B11 Homo sapiens Q8NBQ5 32296183
种属内
SYS1 Q8N2H4 ELOVL5 Homo sapiens Q9NYP7 32296183
种属内
SYS1 Q8N2H4 ELOVL5 Homo sapiens Q9NYP7 32296183
种属内
SYS1 Q8N2H4 ELOVL5 Homo sapiens Q9NYP7 32296183
种属内
SYS1 Q8N2H4 KIR3DL3 Homo sapiens Q8N743 32296183
种属内
SYS1 Q8N2H4 KIR3DL3 Homo sapiens Q8N743 32296183
种属内
SYS1 Q8N2H4 KIR3DL3 Homo sapiens Q8N743 32296183
种属内
SYS1 Q8N2H4 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
种属内
SYS1 Q8N2H4 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
种属内
SYS1 Q8N2H4 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
种属内
SYS1 Q8N2H4 IL3RA Homo sapiens P26951 32296183
种属内
SYS1 Q8N2H4 IL3RA Homo sapiens P26951 32296183
种属内
SYS1 Q8N2H4 BTNL9 Homo sapiens Q6UXG8-3 32296183
种属内
SYS1 Q8N2H4 BTNL9 Homo sapiens Q6UXG8-3 32296183
种属内
SYS1 Q8N2H4 MCFD2 Homo sapiens Q8NI22 32296183
种属内
SYS1 Q8N2H4 MCFD2 Homo sapiens Q8NI22 32296183
种属内
SYS1 Q8N2H4 MCFD2 Homo sapiens Q8NI22 32296183
种属内
SYS1 Q8N2H4 EBP Homo sapiens Q15125 32296183
种属内
SYS1 Q8N2H4 EBP Homo sapiens Q15125 32296183
种属内
SYS1 Q8N2H4 PVR Homo sapiens P15151 32296183
种属内
SYS1 Q8N2H4 TNFSF14 Homo sapiens O43557 32296183
种属内
SYS1 Q8N2H4 TNFSF14 Homo sapiens O43557 32296183
种属内
SYS1 Q8N2H4 TM4SF19 Homo sapiens Q96DZ7 32296183
种属内
SYS1 Q8N2H4 TM4SF19 Homo sapiens Q96DZ7 32296183
种属内
SYS1 Q8N2H4 TM4SF19 Homo sapiens Q96DZ7 32296183
种属内
SYS1 Q8N2H4 MGST3 Homo sapiens O14880 32296183
种属内
SYS1 Q8N2H4 MGST3 Homo sapiens O14880 32296183
种属内
SYS1 Q8N2H4 MRPS18B Homo sapiens Q9Y676 32296183
种属内
SYS1 Q8N2H4 MRPS18B Homo sapiens Q9Y676 32296183
种属内
SYS1 Q8N2H4 MRPS18B Homo sapiens Q9Y676 32296183
种属内
SYS1 Q8N2H4 ERGIC3 Homo sapiens Q9Y282 32296183
种属内
SYS1 Q8N2H4 ERGIC3 Homo sapiens Q9Y282 32296183
种属内
SYS1 Q8N2H4 ERGIC3 Homo sapiens Q9Y282 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
Alkuraya-Kucinskas Syndrome

ALKKUCS

Kiaa1109-Related Early Lethal Congenital Brain Malformations-Arthrogryposis Syndrome

Arthrogryposis

Limited Scleroderma

Limited Cutaneous Systemic Sclerosis

Limited Systemic Sclerosis

Systemic Sclerosis Sine Scleroderma

Crest Syndrome

Limited Cutaneous Systemic Scleroderma

Scleroderma, Limited

Systemic Sclerosis, Limited

Progressive Systemic Sclerosis Sine Scleroderma

Scleroderma, Sine

Crest - [Calcinosis, Raynaud Phenomenon, Oesophageal Dysmotility, Sclerodactyly, And Telangiectasia] Syndrome

Crst - [Calcinosis, Raynaud Phenomenon, Sclerodactyly And Telangiectasia] 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
Bos taurus SYS1 VGNC VGNC:97315
Canis familiaris SYS1 VGNC VGNC:54736
Mus musculus SYS1 MGD MGI:1913710
Rattus norvegicus SYS1 RGD RGD:1583224