STX16

From Wikipedia, the free encyclopedia
Syntaxin 16
Identifiers
SymbolsSTX16; SYN16
External IDsOMIM: 603666 MGI: 1923396 HomoloGene: 2791 GeneCards: STX16 Gene
Orthologs
SpeciesHumanMouse
Entrez8675228960
EnsemblENSG00000124222ENSMUSG00000027522
UniProtO14662Q8BVI5
RefSeq (mRNA)NM_001001433NM_001102423
RefSeq (protein)NP_001001433NP_001095893
Location (UCSC)Chr 20:
57.23 – 57.25 Mb
Chr 2:
174.08 – 174.1 Mb
PubMed search

Syntaxin-16 is a protein that in humans is encoded by the STX16 gene.[1][2][3][4]

It has been associated with pseudohypoparathyroidism type Ib.[3]

Interactions

STX16 has been shown to interact with VAMP4.[5]

References

  1. Tang BL, Low DY, Lee SS, Tan AE, Hong W (Mar 1998). "Molecular cloning and localization of human syntaxin 16, a member of the syntaxin family of SNARE proteins". Biochem Biophys Res Commun 242 (3): 673–9. doi:10.1006/bbrc.1997.8029. PMID 9464276. 
  2. Simonsen A, Bremnes B, Ronning E, Aasland R, Stenmark H (Jun 1998). "Syntaxin-16, a putative Golgi t-SNARE". Eur J Cell Biol 75 (3): 223–31. doi:10.1016/S0171-9335(98)80116-7. PMID 9587053. 
  3. 3.0 3.1 Linglart A, Gensure RC, Olney RC, Juppner H, Bastepe M (Apr 2005). "A novel STX16 deletion in autosomal dominant pseudohypoparathyroidism type Ib redefines the boundaries of a cis-acting imprinting control element of GNAS". Am J Hum Genet 76 (5): 804–14. doi:10.1086/429932. PMC 1199370. PMID 15800843. 
  4. "Entrez Gene: STX16 syntaxin 16". 
  5. Mallard, Frédéric; Tang Bor Luen, Galli Thierry, Tenza Danièle, Saint-Pol Agnès, Yue Xu, Antony Claude, Hong Wanjin, Goud Bruno, Johannes Ludger (Feb 2002). "Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform". J. Cell Biol. (United States) 156 (4): 653–64. doi:10.1083/jcb.200110081. ISSN 0021-9525. PMC 2174079. PMID 11839770. 

Further reading


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