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STX12

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STX12
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSTX12, STX13, STX14, syntaxin 12
External IDsOMIM: 606892; MGI: 1931027; HomoloGene: 128192; GeneCards: STX12; OMA:STX12 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_177424

NM_133887

RefSeq (protein)

NP_803173

NP_598648

Location (UCSC)Chr 1: 27.77 – 27.82 MbChr 4: 132.58 – 132.61 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Syntaxin-12 is a protein that in humans is encoded by the STX12 gene.[5][6]

Interactions

STX12 has been shown to interact with PLDN.[7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000117758Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028879Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Tang BL, Tan AE, Lim LK, Lee SS, Low DY, Hong W (March 1998). "Syntaxin 12, a member of the syntaxin family localized to the endosome". The Journal of Biological Chemistry. 273 (12): 6944–50. doi:10.1074/jbc.273.12.6944. PMID 9507000.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  6. ^ "Entrez Gene: STX12 syntaxin 12".
  7. ^ Huang L, Kuo YM, Gitschier J (November 1999). "The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency". Nature Genetics. 23 (3): 329–32. doi:10.1038/15507. PMID 10610180.

Further reading