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STX16

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens

STX16
Identifiers
AliasesSTX16, SYN16, syntaxin 16, SYN-16
External IDsOMIM:603666;MGI:1923396;HomoloGene:2791;GeneCards:STX16;OMA:STX16 - orthologs
Gene location (Human)
Chromosome 20 (human)
Chr.Chromosome 20 (human)[1]
Chromosome 20 (human)
Genomic location for STX16
Genomic location for STX16
Band20q13.32Start58,651,253bp[1]
End58,679,526bp[1]
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)[2]
Chromosome 2 (mouse)
Genomic location for STX16
Genomic location for STX16
Band2|2 H4Start173,918,101bp[2]
End173,941,564bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right uterine tube

  • sural nerve

  • corpus callosum

  • superficial temporal artery

  • pituitary gland

  • right hemisphere of cerebellum

  • body of uterus

  • C1 segment

  • right ovary

  • anterior pituitary
Top expressed in
  • hand

  • neural layer of retina

  • otolith organ

  • utricle

  • thymus

  • lens

  • cerebellar cortex

  • primary visual cortex

  • yolk sac

  • superior frontal gyrus
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo /QuickGO
Orthologs
SpeciesHumanMouse
Entrez

8675

228960

Ensembl

ENSG00000124222

ENSMUSG00000027522

UniProt

O14662

Q8BVI5

RefSeq (mRNA)
NM_001001433
NM_001001434
NM_001134772
NM_001134773
NM_001204868

NM_003763

NM_001102423
NM_001102424
NM_001102425
NM_172675
NM_001363029

NM_001363030
NM_001363031

RefSeq (protein)

NP_001001433
NP_001128244
NP_001128245
NP_001191797
NP_003754

NP_001095893
NP_001095894
NP_001095895
NP_766263
NP_001349958

NP_001349959
NP_001349960

Location (UCSC)Chr 20: 58.65 – 58.68 MbChr 2: 173.92 – 173.94 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Syntaxin-16 is aprotein that in humans is encoded by theSTX16gene.[5][6][7][8]

It has been associated withpseudohypoparathyroidism type Ib. Losing this gene causes loss of methylation atGNAS1 exon A/B.[7]

Interactions

[edit]

STX16 has been shown tointeract withVAMP4.[9]

References

[edit]
  1. ^abcGRCh38: Ensembl release 89: ENSG00000124222Ensembl, May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000027522Ensembl, 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, Low DY, Lee SS, Tan AE, Hong W (January 1998). "Molecular cloning and localization of human syntaxin 16, a member of the syntaxin family of SNARE proteins".Biochemical and Biophysical Research Communications.242 (3):673–679.Bibcode:1998BBRC..242..673T.doi:10.1006/bbrc.1997.8029.PMID 9464276.
  6. ^Simonsen A, Bremnes B, Rønning E, Aasland R, Stenmark H (March 1998). "Syntaxin-16, a putative Golgi t-SNARE".European Journal of Cell Biology.75 (3):223–231.doi:10.1016/S0171-9335(98)80116-7.PMID 9587053.
  7. ^abLinglart A, Gensure RC, Olney RC, Jüppner H, Bastepe M (May 2005)."A novel STX16 deletion in autosomal dominant pseudohypoparathyroidism type Ib redefines the boundaries of a cis-acting imprinting control element of GNAS".American Journal of Human Genetics.76 (5):804–814.doi:10.1086/429932.PMC 1199370.PMID 15800843.
  8. ^"Entrez Gene: STX16 syntaxin 16".
  9. ^Mallard F, Tang BL, Galli T, Tenza D, Saint-Pol A, Yue X, et al. (February 2002)."Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform".The Journal of Cell Biology.156 (4):653–664.doi:10.1083/jcb.200110081.PMC 2174079.PMID 11839770.

Further reading

[edit]
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
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