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  2. STX5 - syntaxin 5 Gene

STX5 - syntaxin 5 Gene

中文名称:突触 5

种属: Homo sapiens

同用名: SED5; STX5A

基因 ID: 6811 | 基因类型: protein coding

关于 STX5

Cytogenetic location: 11q12.3 Genomic coordinates (GRCh38): 11:62,806,860-62,832,051 (from NCBI)

This gene has 9 transcripts (splice variants), 209 orthologues and 12 paralogues. Ubiquitous expression in thyroid (RPKM 22.3), ovary (RPKM 17.5) and 25 other tissues.

功能概要

该基因编码突触融合蛋白或 t-SNARE (目标 SNAP 受体) 家族的成员。这些蛋白质存在于细胞膜上并作为 v-SNARE (囊泡-SNAP 受体) 的靶标,允许特定的突触囊泡对接和融合。编码的蛋白质调节内质网到高尔基体的运输,并在自噬中起关键作用。针对编码蛋白的自身抗体可能是子宫内膜异位症的诊断标志物。已经观察到该基因编码多种亚型的可变剪接转录物变体。[RefSeq 提供,2011 年 9 月]

This gene encodes a member of the syntaxin or t-SNARE (target-SNAP receptor) family. These proteins are found on cell membranes and serve as the targets for v-SNAREs (vesicle-SNAP receptors), permitting specific synaptic vesicle docking and fusion. The encoded protein regulates endoplasmic reticulum to Golgi transport and plays a critical role in Autophagy. Autoantibodies targeting the encoded protein may be a diagnostic marker for endometriosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]

STX5 基因产物(3)

mRNA Protein Name
NM_001244666.3 NP_001231595.1 syntaxin-5 isoform 2
NM_001330294.2 NP_001317223.1 syntaxin-5 isoform 3
NM_003164.5 NP_003155.2 syntaxin-5 isoform 1
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 SNAP receptor activity IDA
IDA: 通过直接分析推断
15215310 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16189514 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in Golgi disassembly IDA
IDA: 通过直接分析推断
16081076 GOA
involved in early endosome to Golgi transport IMP
IMP: 通过突变表型推断
17389686 GOA
involved in positive regulation of protein catabolic process IMP
IMP: 通过突变表型推断
21242315 GOA
involved in regulation of Golgi organization IDA
IDA: 通过直接分析推断
16081076 GOA
involved in retrograde transport, endosome to Golgi IDA
IDA: 通过直接分析推断
15215310 GOA
involved in retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum IMP
IMP: 通过突变表型推断
34711829 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in Golgi apparatus IDA
IDA: 通过直接分析推断
9464276 GOA
located in vesicle IDA
IDA: 通过直接分析推断
16081076 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

STX5 蛋白结构

Syntaxin

Syntaxin: Syntaxin (91 - 194)

SNARE

SNARE: SNARE domain (269 - 327)

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

syntaxin-5

syntaxin 5A

STX5 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 STX5 Q13190 RETREG3 Homo sapiens Q86VR2
Y2H Prey Pooling
32296183
Intra STX5 Q13190 RETREG3 Homo sapiens Q86VR2
Validated Y2H
32296183
Intra STX5 Q13190 RETREG3 Homo sapiens Q86VR2
Y2H Array
32296183
Intra STX5 Q13190 JAGN1 Homo sapiens Q8N5M9
Y2H Prey Pooling
32296183
Intra STX5 Q13190 JAGN1 Homo sapiens Q8N5M9
Y2H Array
32296183
Intra STX5 Q13190 JAGN1 Homo sapiens Q8N5M9
Validated Y2H
32296183
Intra STX5 Q13190 MAGEA6 Homo sapiens P43360
Validated Y2H
25416956
Intra STX5 Q13190 HSD17B11 Homo sapiens Q8NBQ5
Validated Y2H
32296183
Intra STX5 Q13190 HSD17B11 Homo sapiens Q8NBQ5
Y2H Prey Pooling
32296183
Intra STX5 Q13190 HSD17B11 Homo sapiens Q8NBQ5
Y2H Array
32296183
Intra STX5 Q13190 SEC22B Homo sapiens O75396
Anti Tag CoIP
35271311
Intra STX5 Q13190 STX2 Homo sapiens P32856-2
Y2H Prey Pooling
32296183
Intra STX5 Q13190 STX2 Homo sapiens P32856-2
Y2H Array
32296183
Intra STX5 Q13190 DRC12 Homo sapiens Q494R4-2
Y2H Prey Pooling
32296183
Intra STX5 Q13190 DRC12 Homo sapiens Q494R4-2
Validated Y2H
32296183
Intra STX5 Q13190 DRC12 Homo sapiens Q494R4-2
Y2H Array
32296183
Intra STX5 Q13190 AQP6 Homo sapiens Q13520
Validated Y2H
32296183
Intra STX5 Q13190 AQP6 Homo sapiens Q13520
Y2H Array
32296183
Intra STX5 Q13190 AQP6 Homo sapiens Q13520
Y2H Prey Pooling
32296183
Intra STX5 Q13190 GPR152 Homo sapiens Q8TDT2
Validated Y2H
32296183
Intra STX5 Q13190 GPR152 Homo sapiens Q8TDT2
Y2H Array
32296183
Intra STX5 Q13190 GPR152 Homo sapiens Q8TDT2
Y2H Prey Pooling
32296183
Intra STX5 Q13190 STX3 Homo sapiens Q13277
Validated Y2H
32296183
Intra STX5 Q13190 CRB3 Homo sapiens Q9BUF7-2
Y2H Array
32296183
Intra STX5 Q13190 CRB3 Homo sapiens Q9BUF7-2
Validated Y2H
32296183
Intra STX5 Q13190 CRB3 Homo sapiens Q9BUF7-2
Y2H Prey Pooling
32296183
Intra STX5 Q13190 MTUS1 Homo sapiens Q9ULD2-3
Validated Y2H
32296183
Intra STX5 Q13190 MTUS1 Homo sapiens Q9ULD2-3
Y2H Array
32296183
Intra STX5 Q13190 MTUS1 Homo sapiens Q9ULD2-3
Y2H Prey Pooling
32296183
Intra STX5 Q13190 HSD17B13 Homo sapiens Q7Z5P4
Validated Y2H
32296183
Intra STX5 Q13190 HSD17B13 Homo sapiens Q7Z5P4
Y2H Prey Pooling
32296183
Intra STX5 Q13190 HSD17B13 Homo sapiens Q7Z5P4
Y2H Array
32296183
Intra STX5 Q13190 FAM209A Homo sapiens Q5JX71
Y2H Prey Pooling
32296183
Intra STX5 Q13190 FAM209A Homo sapiens Q5JX71
Validated Y2H
32296183
Intra STX5 Q13190 FAM209A Homo sapiens Q5JX71
Y2H Array
32296183
Intra STX5 Q13190 STING1 Homo sapiens Q86WV6
Y2H Prey Pooling
32296183
Intra STX5 Q13190 STING1 Homo sapiens Q86WV6
Validated Y2H
32296183
Intra STX5 Q13190 STING1 Homo sapiens Q86WV6
Y2H Array
32296183
Intra STX5 Q13190 COG4 Homo sapiens Q9H9E3
Pull Down
19536132
Intra STX5 Q13190 EBP Homo sapiens Q15125
Validated Y2H
32296183
Intra STX5 Q13190 EBP Homo sapiens Q15125
Y2H Prey Pooling
32296183
Intra STX5 Q13190 EBP Homo sapiens Q15125
Y2H Array
32296183
Intra STX5 Q13190 NAPB Homo sapiens Q9H115
Validated Y2H
32296183
Intra STX5 Q13190 NAPB Homo sapiens Q9H115
Y2H Prey Pooling
32296183
Intra STX5 Q13190 NAPB Homo sapiens Q9H115
Y2H Array
32296183
Intra STX5 Q13190 NAPB Homo sapiens Q9H115
Y2H Prey Pooling
25416956
Intra STX5 Q13190 LRRC4C Homo sapiens Q9HCJ2
Validated Y2H
32296183
Intra STX5 Q13190 LRRC4C Homo sapiens Q9HCJ2
Y2H Array
32296183
Intra STX5 Q13190 LRRC4C Homo sapiens Q9HCJ2
Y2H Prey Pooling
32296183
Intra STX5 Q13190 GOSR2 Homo sapiens O14653
Y2H Array
32296183
Intra STX5 Q13190 GOSR2 Homo sapiens O14653
Anti Tag CoIP
35271311
Intra STX5 Q13190 GOSR2 Homo sapiens O14653
Y2H Prey Pooling
32296183
Intra STX5 Q13190 AARD Homo sapiens Q4LEZ3
Validated Y2H
32296183
Intra STX5 Q13190 TACC1 Homo sapiens O75410
Y2H Array
25416956
Intra STX5 Q13190 STX1A Homo sapiens Q16623
Y2H Array
32296183
Intra STX5 Q13190 STX1A Homo sapiens Q16623
Y2H Prey Pooling
32296183
Intra STX5 Q13190 STX1A Homo sapiens Q16623
Validated Y2H
32296183
Intra STX5 Q13190 STX8 Homo sapiens Q9UNK0
Validated Y2H
32296183
Intra STX5 Q13190 STX8 Homo sapiens Q9UNK0
Y2H Prey Pooling
32296183
Intra STX5 Q13190 STX8 Homo sapiens Q9UNK0
Y2H Array
32296183
Intra STX5 Q13190 STX4 Homo sapiens Q12846
Y2H Prey Pooling
32296183
Intra STX5 Q13190 STX4 Homo sapiens Q12846
Y2H Array
32296183
Intra STX5 Q13190 KASH5 Homo sapiens Q8N6L0
Y2H Array
32296183
Intra STX5 Q13190 KASH5 Homo sapiens Q8N6L0
Validated Y2H
25416956
Intra STX5 Q13190 KASH5 Homo sapiens Q8N6L0
Y2H Prey Pooling
32296183
Intra STX5 Q13190 KASH5 Homo sapiens Q8N6L0
Validated Y2H
32296183
Intra STX5 Q13190 NAPA Homo sapiens P54920
Anti Tag CoIP
35271311
Intra STX5 Q13190 NAPA Homo sapiens P54920
Y2H Pooling
16189514
Intra STX5 Q13190 REEP4 Homo sapiens Q9H6H4
Y2H Array
32296183
Intra STX5 Q13190 REEP4 Homo sapiens Q9H6H4
Y2H Prey Pooling
32296183
Intra STX5 Q13190 REEP4 Homo sapiens Q9H6H4
Validated Y2H
32296183
Intra STX5 Q13190 CREB3L3 Homo sapiens Q68CJ9
Validated Y2H
32296183
Intra STX5 Q13190 CREB3L3 Homo sapiens Q68CJ9
Y2H Prey Pooling
32296183
Intra STX5 Q13190 CREB3L3 Homo sapiens Q68CJ9
Y2H Array
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
Human Cytomegalovirus Infection

Cytomegalovirus Infection

Cytomegalovirus Infections

Endometriosis

Endometriosis, Site Unspecified

Endometrial Ectopia

Spondyloepiphyseal Dysplasia, Nishimura Type

SEDN

Spondyloepiphyseal Dysplasia Nishimura Type

Charcot-Marie-Tooth Disease, Axonal, Type 2z

CMT2Z

Charcot-Marie-Tooth Disease Axonal Type 2z

Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2z

Charcot-Marie-Tooth Neuropathy, Type 2z

Autosomal Dominant Axonal Charcot-Marie-Tooth Disease Type 2z

Charcot-Marie-Tooth Neuropathy Type 2z

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2z

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Morc2 Mutation

Charcot-Marie-Tooth Disease 2z

Charcot-Marie-Tooth Disease, Type 2z

Smith-Mccort Dysplasia 1

Smith-Mccort Dysplasia

SMC1

Smc

Smith Mccort Dysplasia

Smith-Mccort Dwarfism

Congenital Disorder Of Glycosylation, Type Iih

CDG2H

Congenital Disorder Of Glycosylation Type Iih

Cdg Iih

Cdgiih

Carbohydrate Deficient Glycoprotein Syndrome Type Iih

Congenital Disorder Of Glycosylation Type 2h

Cog8-Cdg

Cdg-Iih

Cdgiidh

Cdg Syndrome Type Iih

Congenital Disorder Of Glycosylation 2h

Glycosylation, Congenital Disorder Of, Type Iih

Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome

Cednik Syndrome

CEDNIK

Cerebral Dysgenesis, Neuropathy, Ichthyosis And Keratoderma Syndrome

Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndro

Cerebral Dysgenesis-Neuropathy-Ichthyosis-Palmoplantar Keratoderma Syndrome

Cerebral Dysgenesis-Neuropathy-Ichthyosis-Keratoderma Syndrome

Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma

Neurocutaneous Syndromes

Dyggve-Melchior-Clausen Disease

Dyggve-Melchior-Clausen Syndrome

DMC

Dmc Disease

Pseudo-Morquio Disease Type I

Dmc Syndrome

Cataract 4, Multiple Types

Cataract 4 Multiple Types

CTRCT4

Cca3

Pcc

Aculeiform Cataract

Cataract 4, Multiple Types, With Or Without Microcornea

Cataract, Crystalline Aculeiform

Caca

Cataract, Congenital, Cerulean Type, 3

Congenital Cataract Cerulean Type 3

Cataract Congenital Dominant Non Nuclear

Ccp

Cataract, Nonnuclear Polymorphic Congenital

Cataract, Punctate, Progressive Juvenile-Onset

Cataract 4 Multiple Types With Or Without Microcornea

Autosomal Dominant Nonnuclear Polymorphic Congenital Cataract

Cataract, Polymorphic Congenital

Congenital Cataract Blue Dot Type 3

Congenital Non-Nuclear Polymorphic Cataract

Crystalline Aculeiform Cataract

Punctate, Progressive Juvenile-Onset, Cataract

Cataract, Nonnuclear Polymorphic Congenital, Autosomal Dominant

Congenital Disorder Of Glycosylation, Type In

Congenital Disorder Of Glycosylation

CDG1N

Congenital Disorders Of Glycosylation

Cdg In

Cdgin

Congenital Disorder Of Glycosylation 1n

Carbohydrate-Deficient Glycoprotein Syndrome

Cdg

Rft1-Cdg

Cdg-In

Congenital Disorder Of Glycosylation Type In

Carbohydrate Deficient Glycoprotein Syndrome

Cdg Syndrome

Congenital Disorder Of Glycosylation In

Carbohydrate-Deficient Glycoprotein Syndromes

Cdg Syndrome Type In

Carbohydrate Deficient Glycoprotein Syndrome Type In

Congenital Disorder Of Glycosylation Type 1n

Man5glcnac2-Pp-Dol Flippase Deficiency

Glycosylation, Congenital Disorder Of

Glycosylation, Congenital Disorder Of, Type In

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
Canis familiaris STX5 VGNC VGNC:46957
Macaca mulatta STX5 VGNC VGNC:78045
Felis catus STX5 VGNC VGNC:65815
Mus musculus STX5 MGD MGI:1928483
Rattus norvegicus STX5 RGD RGD:68426
Bos taurus STX5 VGNC VGNC:35441