STX17
Sign in to saveAlso known as syntaxin 17
Syntaxin 17 is a protein that in humans is encoded by the STX17 gene. In horses a duplication in intron 6 causes progressive graying.
Gene data
STX17- Name
- syntaxin 17
- Type
- protein-coding
- Position
- 99,906,654–99,974,534 (+)
- Ensembl
- ENSG00000136874
- RefSeq RNA
- NM_017919.3, XM_011518820.4, XM_011518821.4, XM_011518823.4, XM_047423551.1
- RefSeq protein
- NP_060389.2, XP_011517122.1, XP_011517123.1, XP_011517125.1, XP_047279507.1
Enables SNAP receptor activity; SNARE binding activity; and protein phosphatase binding activity. Involved in several processes, including autophagosome membrane docking; endoplasmic reticulum to Golgi vesicle-mediated transport; and endoplasmic reticulum-Golgi intermediate compartment organization. Acts upstream of or within protein localization to phagophore assembly site. Located in several cellular components, including autophagosome membrane; endoplasmic reticulum-Golgi intermediate compartment; and mitochondria-associated endoplasmic reticulum membrane. Part of SNARE complex. Colocalizes with HOPS complex. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
syntaxin 17
- Symbol
- STX17
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 9:99,906,654-99,974,534
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 9917
- exact match
- identifiers.org/ncbigene/55014
- genomic end
- 99974534
- genomic start
- 99906654
- cytogenetic location
- 9q31.1
via Wikidata · CC0
~1 min read
Article
4 sectionsContents
- See also
- References
- Further reading
- External links
Syntaxin 17 is a protein that in humans is encoded by the STX17 gene. In horses a duplication in intron 6 causes progressive graying.
==See also== Syntaxin