STX17

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]

STX17
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSTX17, syntaxin 17
External IDsOMIM: 604204 MGI: 1914977 HomoloGene: 9917 GeneCards: STX17
Gene location (Human)
Chr.Chromosome 9 (human)[1]
Band9q31.1Start99,906,654 bp[1]
End99,974,534 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

55014

67727

Ensembl

ENSG00000136874

ENSMUSG00000061455

UniProt

P56962

Q9D0I4

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

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000136874 - Ensembl, May 2017
  2. 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

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


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