Article · Wikipedia archive · Last revised Jun 25, 2026

STX17

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

Last revised
Jun 25, 2026
Read time
≈ 2 min
Length
558 w
Citations
10
Source
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 search34
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

See also

References

References

  1. GRCh38: Ensembl release 89: ENSG00000136874Ensembl, May 2017
  2. 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

Further reading

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