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STX12

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Protein-coding gene in the species Homo sapiens
STX12
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2DNX

Identifiers
AliasesSTX12, STX13, STX14, syntaxin 12
External IDsOMIM: 606892; MGI: 1931027; HomoloGene: 128192; GeneCards: STX12; OMA:STX12 - orthologs
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)
Chromosome 1 (human)Genomic location for STX12Genomic location for STX12
Band1p35.3Start27,773,219 bp
End27,824,443 bp
Gene location (Mouse)
Chromosome 4 (mouse)
Chr.Chromosome 4 (mouse)
Chromosome 4 (mouse)Genomic location for STX12Genomic location for STX12
Band4 D2.3|4 66.01 cMStart132,580,812 bp
End132,611,820 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • middle temporal gyrus

  • corpus epididymis

  • Brodmann area 23

  • left lobe of thyroid gland

  • right lobe of thyroid gland

  • lower lobe of lung

  • tail of epididymis

  • superior frontal gyrus

  • pars reticulata

  • Brodmann area 46
Top expressed in
  • transitional epithelium of urinary bladder

  • medial ganglionic eminence

  • pyloric antrum

  • Amygdala

  • Region I of hippocampus proper

  • habenula

  • cingulate gyrus

  • paraventricular nucleus of hypothalamus

  • arcuate nucleus

  • dorsomedial hypothalamic nucleus
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

23673

100226

Ensembl

ENSG00000117758

ENSMUSG00000028879

UniProt

Q86Y82

Q9ER00

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
Wikidata
View/Edit HumanView/Edit Mouse

Syntaxin-12 is a protein that in humans is encoded by the STX12 gene.

Interactions

STX12 has been shown to interact with PLDN.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000117758Ensembl, May 2017
  2. ^ 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.
  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. S2CID 22843205.

Further reading

External links

  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Syntaxin-12


PDB gallery
  • 2dnx: Solution structure of RSGI RUH-063, an N-terminal domain of Syntaxin 12 from human cDNA 2dnx: Solution structure of RSGI RUH-063, an N-terminal domain of Syntaxin 12 from human cDNA
  • 2nps: Crystal Structure of the Early Endosomal SNARE Complex 2nps: Crystal Structure of the Early Endosomal SNARE Complex
Membrane protein: vesicular transport proteins (TC 1F)
Synaptic vesicle
SNARE
Q-SNARE
R-SNARE
Synaptotagmin
Other
COPI
COPII
RME/Clathrin
Caveolae
Other/ungrouped
Vesicle formation
Adaptor protein complex 1:
Adaptor protein complex 2:
Adaptor protein complex 3:
Adaptor protein complex 4:
BLOC-1:
BLOC-2:
BLOC-3:
Coats:
Small GTPase
Other
See also vesicular transport protein disorders


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