1. Gene
  2. STX6 - syntaxin 6 Gene

STX6 - syntaxin 6 Gene

Homo sapiens
Gene ID: 10228 | Gene type: protein coding

About STX6

Cytogenetic location: 1q25.3 Genomic coordinates (GRCh38): 1:180,972,725-181,022,870 (from NCBI)

This gene has 4 transcripts (splice variants), 206 orthologues and 2 paralogues. Ubiquitous expression in brain (RPKM 10.0), esophagus (RPKM 7.6) and 24 other tissues.

Summary

Enables syntaxin binding activity. Involved in several processes, including Golgi ribbon formation; retrograde transport, endosome to Golgi; and vesicle fusion. Acts upstream of or within endocytic recycling. Located in several cellular components, including early endosome; perinuclear region of cytoplasm; and trans-Golgi network. Part of SNARE complex. [provided by Alliance of Genome Resources, Apr 2022]

STX6 Products(2)

mRNA Protein Name
NM_001286210.2 NP_001273139.1 syntaxin-6 isoform 2
NM_005819.6 NP_005810.1 syntaxin-6 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
11384996 GOA
enables syntaxin binding IPI
IPI: Inferred from physical interaction
16154903 GOA
Biological Process GO Annotation Evidence Reference Source
acts upstream of or within endocytic recycling IMP
IMP: Inferred from mutant phenotype
25799061 GOA
involved in endocytic recycling IMP
IMP: Inferred from mutant phenotype
23677696 GOA
involved in regulation of protein localization IMP
IMP: Inferred from mutant phenotype
16154903 GOA
involved in retrograde transport, endosome to Golgi IMP
IMP: Inferred from mutant phenotype
19224922 GOA
involved in vesicle fusion IPI
IPI: Inferred from physical interaction
10506127 GOA
Cellular Component GO Annotation Evidence Reference Source
located in Golgi apparatus IDA
IDA: Inferred from direct assay
19224922 GOA
part of SNARE complex IDA
IDA: Inferred from direct assay
19620288 GOA
located in early endosome IDA
IDA: Inferred from direct assay
10506127 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
10506127 GOA
located in trans-Golgi network IDA
IDA: Inferred from direct assay
16154903 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

STX6 Protein Structure

Syntaxin-6_N

Syntaxin-6_N: Syntaxin 6, N-terminal (5 - 103)

SNARE

SNARE: SNARE domain (168 - 228)

  • 0
  • 100
  • 200
  • 255 a.a.
Protein Preferred Names Protein Names

syntaxin-6

STX6 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
STX6 O43752 ARMC8 Homo sapiens Q8IUR7-6 32296183
Intra
STX6 O43752 ARMC8 Homo sapiens Q8IUR7-6 32296183
Intra
STX6 O43752 ARMC8 Homo sapiens Q8IUR7-6 32296183
Intra
STX6 O43752 STX2 Homo sapiens P32856-2 32296183
Intra
STX6 O43752 STX2 Homo sapiens P32856-2 32296183
Intra
STX6 O43752 STX2 Homo sapiens P32856-2 32296183
Intra
STX6 O43752 STOM Homo sapiens P27105 32296183
Intra
STX6 O43752 STOM Homo sapiens P27105 32296183
Intra
STX6 O43752 STOM Homo sapiens P27105 32296183
Intra
STX6 O43752 AQP6 Homo sapiens Q13520 32296183
Intra
STX6 O43752 AQP6 Homo sapiens Q13520 32296183
Intra
STX6 O43752 AQP6 Homo sapiens Q13520 32296183
Intra
STX6 O43752 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
STX6 O43752 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
STX6 O43752 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
STX6 O43752 SCN3B Homo sapiens Q9NY72 32296183
Intra
STX6 O43752 SCN3B Homo sapiens Q9NY72 32296183
Intra
STX6 O43752 SCN3B Homo sapiens Q9NY72 32296183
Intra
STX6 O43752 MTERF2 Homo sapiens Q49AM1 32296183
Intra
STX6 O43752 MTERF2 Homo sapiens Q49AM1 32296183
Intra
STX6 O43752 MTERF2 Homo sapiens Q49AM1 32296183
Intra
STX6 O43752 FAM210B Homo sapiens Q96KR6 32296183
Intra
STX6 O43752 FAM210B Homo sapiens Q96KR6 32296183
Intra
STX6 O43752 FAM210B Homo sapiens Q96KR6 32296183
Intra
STX6 O43752 TMEM86B Homo sapiens Q8N661 32296183
Intra
STX6 O43752 TMEM86B Homo sapiens Q8N661 32296183
Intra
STX6 O43752 TMEM86B Homo sapiens Q8N661 32296183
Intra
STX6 O43752 LIME1 Homo sapiens Q9H400 32296183
Intra
STX6 O43752 LIME1 Homo sapiens Q9H400 32296183
Intra
STX6 O43752 LIME1 Homo sapiens Q9H400 32296183
Intra
STX6 O43752 PSMA3 Homo sapiens P25788 25416956
Intra
STX6 O43752 EBP Homo sapiens Q15125 32296183
Intra
STX6 O43752 EBP Homo sapiens Q15125 32296183
Intra
STX6 O43752 EBP Homo sapiens Q15125 32296183
Intra
STX6 O43752 NAPB Homo sapiens Q9H115 25416956
Intra
STX6 O43752 NAPB Homo sapiens Q9H115 33961781
Intra
STX6 O43752 NAPB Homo sapiens Q9H115 25416956
Intra
STX6 O43752 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
STX6 O43752 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
STX6 O43752 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
STX6 O43752 GOSR2 Homo sapiens O14653 25416956
Intra
STX6 O43752 GOSR2 Homo sapiens O14653 25416956
Intra
STX6 O43752 GOSR2 Homo sapiens O14653 33961781
Intra
STX6 O43752 SNAP29 Homo sapiens O95721 25419848
Intra
STX6 O43752 SNAP29 Homo sapiens O95721 33422265
Intra
STX6 O43752 MMGT1 Homo sapiens Q8N4V1 32296183
Intra
STX6 O43752 MMGT1 Homo sapiens Q8N4V1 32296183
Intra
STX6 O43752 MMGT1 Homo sapiens Q8N4V1 32296183
Intra
STX6 O43752 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
STX6 O43752 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
STX6 O43752 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
STX6 O43752 TMEM205 Homo sapiens Q6UW68 32296183
Intra
STX6 O43752 TMEM205 Homo sapiens Q6UW68 32296183
Intra
STX6 O43752 TMEM205 Homo sapiens Q6UW68 32296183
Intra
STX6 O43752 STX1A Homo sapiens Q16623 32296183
Intra
STX6 O43752 STX1A Homo sapiens Q16623 32296183
Intra
STX6 O43752 STX1A Homo sapiens Q16623 32296183
Intra
STX6 O43752 TMEM9 Homo sapiens Q9P0T7 32296183
Intra
STX6 O43752 TMEM9 Homo sapiens Q9P0T7 32296183
Intra
STX6 O43752 TMEM9 Homo sapiens Q9P0T7 32296183
Intra
STX6 O43752 STX4 Homo sapiens Q12846 33961781
Intra
STX6 O43752 STX4 Homo sapiens Q12846 28514442
Intra
STX6 O43752 STX4 Homo sapiens Q12846 32296183
Intra
STX6 O43752 STX4 Homo sapiens Q12846 32296183
Intra
STX6 O43752 STX4 Homo sapiens Q12846 32296183
Intra
STX6 O43752 APP Homo sapiens P05067 32814053
Intra
STX6 O43752 APP Homo sapiens P05067 32814053
Intra
STX6 O43752 APP Homo sapiens P05067 32814053
Intra
STX6 O43752 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
STX6 O43752 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
STX6 O43752 TMEM14B Homo sapiens Q9NUH8 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant STX6 Proteins

Cat. No. Product Name Accession Purity
HY-P71032 Syntaxin-6 Protein, Human O43752 (S2-Q234) ≥95%

Related Diseases

Diseases Alias
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

Pontocerebellar Hypoplasia, Type 2e

Pontocerebellar Hypoplasia Type 2

Pontocerebellar Hypoplasia Type 2e

Pch2

PCH2E

Progressive Microcephaly From Birth Extrapyramidal Dyskinesia Chorea Epilepsy

Pontocerebellar Hypoplasia 2e

Pcca2

Progressive Cerebello-Cerebral Atrophy Type 2

Doid:0112328

Hypoplasia, Pontocerebellar, Type 2e

Pontocerebellar Hypoplasia, Type 2d

Pontocerebellar Hypoplasia Type 2a

Supranuclear Palsy, Progressive, 1

Progressive Supranuclear Palsy

Steele-Richardson-Olszewski Syndrome

Supranuclear Palsy, Progressive

Progressive Supranuclear Ophthalmoplegia

Psp

PSNP1

Familial Progressive Supranuclear Palsy

Richardson'S Syndrome

Psp Syndrome

Progressive Supranuclear Palsy 1

Supranuclear Palsy Progressive

Ophthalmoplegia, Supranuclear, Progressive

Steele-Richardson-Olszewksi Syndrome

Parkinson Disease, Late-Onset

Parkinson Disease

Parkinson'S Disease

PD

PARK

Parkinson Disease, Susceptibility To

Late Onset Parkinson'S Disease

Late Onset Parkinson Disease

Paralysis Agitans

Primary Parkinsonism

Idiopathic Parkinson Disease

Parkinson'S

Parkinson Disease, Late-Onset, Susceptibility To

Parkinson Disease, Age Of Onset, Modifier

Lewy Body Parkinson Disease

Idiopathic Parkinson'S Disease

Pd - [Parkinson Disease]

Parkinson Disease Nos

Parkinson, Nos

Primary Parkinson Disease

Diseases Alias
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

Orthologs Information

Species Symbol Source ID
Macaca mulatta STX6 VGNC VGNC:78046
Felis catus STX6 VGNC VGNC:65816
Mus musculus STX6 MGD MGI:1926235
Rattus norvegicus STX6 RGD RGD:61915
Bos taurus STX6 VGNC VGNC:35442
Canis familiaris STX6 VGNC VGNC:55762
Others STX6 NCBI