STX17

From Wikipedia the free encyclopedia

STX17
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSTX17, syntaxin 17
External IDsOMIM: 604204; MGI: 1914977; HomoloGene: 9917; GeneCards: STX17; OMA:STX17 - orthologs
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. ^ a b c GRCh38: Ensembl release 89: ENSG00000136874Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000061455Ensembl, 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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  • Overview of all the structural information available in the PDB for UniProt: P56962 (Human Syntaxin-17 (STX17)) at the PDBe-KB.