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STX17

From Wikipedia, the free encyclopedia
STX17
Identifiers
AliasesSTX17, syntaxin 17
External IDsOMIM: 604204; MGI: 1914977; HomoloGene: 9917; GeneCards: STX17; OMA:STX17 - orthologs
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_017919

NM_026343

RefSeq (protein)

NP_060389

NP_080619

Location (UCSC)Chr 9: 99.91 – 99.97 MbChr 4: 48.12 – 48.19 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Syntaxin 17 is a protein that in humans is encoded by the STX17 gene.[5] In horses a duplication in intron 6 causes progressive graying.[6]

See also

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References

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  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000136874 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000061455 Ensembl, 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. "Entrez Gene: Syntaxin 17".
  6. "UC Davis Gray".

Further reading

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[edit]
  • Overview of all the structural information available in the PDB for UniProt: P56962 (Human Syntaxin-17 (STX17)) at the PDBe-KB.