STX5 - syntaxin 5 Gene
Also Known as SED5; STX5A
Species: Homo sapiens
About STX5
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.
Summary
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 Products (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 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables SNAP receptor activity |
IDA
IDA: Inferred from direct assay
|
15215310 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
16189514 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in Golgi disassembly |
IDA
IDA: Inferred from direct assay
|
16081076 | GOA |
| involved in early endosome to Golgi transport |
IMP
IMP: Inferred from mutant phenotype
|
17389686 | GOA |
| involved in positive regulation of protein catabolic process |
IMP
IMP: Inferred from mutant phenotype
|
21242315 | GOA |
| involved in regulation of Golgi organization |
IDA
IDA: Inferred from direct assay
|
16081076 | GOA |
| involved in retrograde transport, endosome to Golgi |
IDA
IDA: Inferred from direct assay
|
15215310 | GOA |
| involved in retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum |
IMP
IMP: Inferred from mutant phenotype
|
34711829 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in Golgi apparatus |
IDA
IDA: Inferred from direct assay
|
9464276 | GOA |
| located in vesicle |
IDA
IDA: Inferred from direct assay
|
16081076 | GOA |
STX5 Protein Structure
Syntaxin: Syntaxin (91 - 194)
SNARE: SNARE domain (269 - 327)
- 0
- 100
- 200
- 300
- 355 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
syntaxin-5 |
|
STX5 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
STX5 | Q13190 | RETREG3 | Homo sapiens | Q86VR2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | RETREG3 | Homo sapiens | Q86VR2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | RETREG3 | Homo sapiens | Q86VR2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | JAGN1 | Homo sapiens | Q8N5M9 | 32296183 | |
|
Intra
|
STX5 | Q13190 | JAGN1 | Homo sapiens | Q8N5M9 | 32296183 | |
|
Intra
|
STX5 | Q13190 | JAGN1 | Homo sapiens | Q8N5M9 | 32296183 | |
|
Intra
|
STX5 | Q13190 | MAGEA6 | Homo sapiens | P43360 | 25416956 | |
|
Intra
|
STX5 | Q13190 | HSD17B11 | Homo sapiens | Q8NBQ5 | 32296183 | |
|
Intra
|
STX5 | Q13190 | HSD17B11 | Homo sapiens | Q8NBQ5 | 32296183 | |
|
Intra
|
STX5 | Q13190 | HSD17B11 | Homo sapiens | Q8NBQ5 | 32296183 | |
|
Intra
|
STX5 | Q13190 | SEC22B | Homo sapiens | O75396 | 35271311 | |
|
Intra
|
STX5 | Q13190 | STX2 | Homo sapiens | P32856-2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX2 | Homo sapiens | P32856-2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | DRC12 | Homo sapiens | Q494R4-2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | DRC12 | Homo sapiens | Q494R4-2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | DRC12 | Homo sapiens | Q494R4-2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | AQP6 | Homo sapiens | Q13520 | 32296183 | |
|
Intra
|
STX5 | Q13190 | AQP6 | Homo sapiens | Q13520 | 32296183 | |
|
Intra
|
STX5 | Q13190 | AQP6 | Homo sapiens | Q13520 | 32296183 | |
|
Intra
|
STX5 | Q13190 | GPR152 | Homo sapiens | Q8TDT2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | GPR152 | Homo sapiens | Q8TDT2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | GPR152 | Homo sapiens | Q8TDT2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX3 | Homo sapiens | Q13277 | 32296183 | |
|
Intra
|
STX5 | Q13190 | CRB3 | Homo sapiens | Q9BUF7-2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | CRB3 | Homo sapiens | Q9BUF7-2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | CRB3 | Homo sapiens | Q9BUF7-2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | MTUS1 | Homo sapiens | Q9ULD2-3 | 32296183 | |
|
Intra
|
STX5 | Q13190 | MTUS1 | Homo sapiens | Q9ULD2-3 | 32296183 | |
|
Intra
|
STX5 | Q13190 | MTUS1 | Homo sapiens | Q9ULD2-3 | 32296183 | |
|
Intra
|
STX5 | Q13190 | HSD17B13 | Homo sapiens | Q7Z5P4 | 32296183 | |
|
Intra
|
STX5 | Q13190 | HSD17B13 | Homo sapiens | Q7Z5P4 | 32296183 | |
|
Intra
|
STX5 | Q13190 | HSD17B13 | Homo sapiens | Q7Z5P4 | 32296183 | |
|
Intra
|
STX5 | Q13190 | FAM209A | Homo sapiens | Q5JX71 | 32296183 | |
|
Intra
|
STX5 | Q13190 | FAM209A | Homo sapiens | Q5JX71 | 32296183 | |
|
Intra
|
STX5 | Q13190 | FAM209A | Homo sapiens | Q5JX71 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STING1 | Homo sapiens | Q86WV6 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STING1 | Homo sapiens | Q86WV6 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STING1 | Homo sapiens | Q86WV6 | 32296183 | |
|
Intra
|
STX5 | Q13190 | COG4 | Homo sapiens | Q9H9E3 | 19536132 | |
|
Intra
|
STX5 | Q13190 | EBP | Homo sapiens | Q15125 | 32296183 | |
|
Intra
|
STX5 | Q13190 | EBP | Homo sapiens | Q15125 | 32296183 | |
|
Intra
|
STX5 | Q13190 | EBP | Homo sapiens | Q15125 | 32296183 | |
|
Intra
|
STX5 | Q13190 | NAPB | Homo sapiens | Q9H115 | 32296183 | |
|
Intra
|
STX5 | Q13190 | NAPB | Homo sapiens | Q9H115 | 32296183 | |
|
Intra
|
STX5 | Q13190 | NAPB | Homo sapiens | Q9H115 | 32296183 | |
|
Intra
|
STX5 | Q13190 | NAPB | Homo sapiens | Q9H115 | 25416956 | |
|
Intra
|
STX5 | Q13190 | LRRC4C | Homo sapiens | Q9HCJ2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | LRRC4C | Homo sapiens | Q9HCJ2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | LRRC4C | Homo sapiens | Q9HCJ2 | 32296183 | |
|
Intra
|
STX5 | Q13190 | GOSR2 | Homo sapiens | O14653 | 32296183 | |
|
Intra
|
STX5 | Q13190 | GOSR2 | Homo sapiens | O14653 | 35271311 | |
|
Intra
|
STX5 | Q13190 | GOSR2 | Homo sapiens | O14653 | 32296183 | |
|
Intra
|
STX5 | Q13190 | AARD | Homo sapiens | Q4LEZ3 | 32296183 | |
|
Intra
|
STX5 | Q13190 | TACC1 | Homo sapiens | O75410 | 25416956 | |
|
Intra
|
STX5 | Q13190 | STX1A | Homo sapiens | Q16623 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX1A | Homo sapiens | Q16623 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX1A | Homo sapiens | Q16623 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX8 | Homo sapiens | Q9UNK0 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX8 | Homo sapiens | Q9UNK0 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX8 | Homo sapiens | Q9UNK0 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX4 | Homo sapiens | Q12846 | 32296183 | |
|
Intra
|
STX5 | Q13190 | STX4 | Homo sapiens | Q12846 | 32296183 | |
|
Intra
|
STX5 | Q13190 | KASH5 | Homo sapiens | Q8N6L0 | 32296183 | |
|
Intra
|
STX5 | Q13190 | KASH5 | Homo sapiens | Q8N6L0 | 25416956 | |
|
Intra
|
STX5 | Q13190 | KASH5 | Homo sapiens | Q8N6L0 | 32296183 | |
|
Intra
|
STX5 | Q13190 | KASH5 | Homo sapiens | Q8N6L0 | 32296183 | |
|
Intra
|
STX5 | Q13190 | NAPA | Homo sapiens | P54920 | 35271311 | |
|
Intra
|
STX5 | Q13190 | NAPA | Homo sapiens | P54920 | 16189514 | |
|
Intra
|
STX5 | Q13190 | REEP4 | Homo sapiens | Q9H6H4 | 32296183 | |
|
Intra
|
STX5 | Q13190 | REEP4 | Homo sapiens | Q9H6H4 | 32296183 | |
|
Intra
|
STX5 | Q13190 | REEP4 | Homo sapiens | Q9H6H4 | 32296183 | |
|
Intra
|
STX5 | Q13190 | CREB3L3 | Homo sapiens | Q68CJ9 | 32296183 | |
|
Intra
|
STX5 | Q13190 | CREB3L3 | Homo sapiens | Q68CJ9 | 32296183 | |
|
Intra
|
STX5 | Q13190 | CREB3L3 | Homo sapiens | Q68CJ9 | 32296183 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Human Cytomegalovirus Infection |
|
|
| Endometriosis |
|
|
| Spondyloepiphyseal Dysplasia, Nishimura Type |
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2z |
|
|
| Smith-Mccort Dysplasia 1 |
|
|
| Congenital Disorder Of Glycosylation, Type Iih |
|
|
| Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome |
|
|
| Dyggve-Melchior-Clausen Disease |
|
|
| Cataract 4, Multiple Types |
|
|
| Congenital Disorder Of Glycosylation, Type In |
|
|
Orthologs Information
| Species | Symbol | Source | 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 |
| Others | STX5 | NCBI |