STX6

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STX6
Protein STX6 PDB 1lvf.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases STX6
External IDs MGI: 1926235 HomoloGene: 115622 GeneCards: STX6
Genetically Related Diseases
progressive supranuclear palsy[1]
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001286210
NM_005819

NM_021433

RefSeq (protein)

NP_001273139
NP_005810

NP_067408.1
NP_067408

Location (UCSC) Chr 1: 180.97 – 181.02 Mb Chr 1: 155.16 – 155.21 Mb
PubMed search [2] [3]
Wikidata
View/Edit Human View/Edit Mouse

Syntaxin-6 is a protein that in humans is encoded by the STX6 gene.[4][5]

Interactions[edit]

STX6 has been shown to interact with SNAP23,[6] VAMP3[7] and VAMP4.[7]

References[edit]

  1. ^ "Diseases that are genetically associated with STX6 view/edit references on wikidata". 
  2. ^ "Human PubMed Reference:". 
  3. ^ "Mouse PubMed Reference:". 
  4. ^ Martín-Martín B, Nabokina SM, Lazo PA, Mollinedo F (Mar 1999). "Co-expression of several human syntaxin genes in neutrophils and differentiating HL-60 cells: variant isoforms and detection of syntaxin 1". Journal of Leukocyte Biology. 65 (3): 397–406. PMID 10080545. 
  5. ^ "Entrez Gene: STX6 syntaxin 6". 
  6. ^ Martín-Martín B, Nabokina SM, Blasi J, Lazo PA, Mollinedo F (Oct 2000). "Involvement of SNAP-23 and syntaxin 6 in human neutrophil exocytosis". Blood. 96 (7): 2574–83. PMID 11001914. 
  7. ^ a b Mallard F, Tang BL, Galli T, Tenza D, Saint-Pol A, Yue X, Antony C, Hong W, Goud B, Johannes L (Feb 2002). "Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform". The Journal of Cell Biology. 156 (4): 653–64. doi:10.1083/jcb.200110081. PMC 2174079Freely accessible. PMID 11839770. 

Further reading[edit]

External links[edit]