STX7
Syntaxin-7
Also known as: STX7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15400
- Gene
- STX7
- Ensembl
- ENSG00000079950
- Chromosome
- 6
- Canonical length
- 261 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Lysosomes
OverviewNCBI Gene
The protein encoded by this gene is a syntaxin family membrane receptor involved in vesicle transport. The encoded protein binds alpha-SNAP, an important regulator of transport vesicle fusion. Along with syntaxin 13, this protein plays a role in the ordered fusion of endosomes and lysosomes with the phagosome. [provided by RefSeq, May 2016]
Canonical amino-acid sequenceUniProt
261 residues, UniProt reviewed canonical sequence.
>O15400|STX7
1 MSYTPGVGGD PAQLAQRISS NIQKITQCSV EIQRTLNQLG TPQDSPELRQ QLQQKQQYTN
61 QLAKETDKYI KEFGSLPTTP SEQRQRKIQK DRLVAEFTTS LTNFQKVQRQ AAEREKEFVA
121 RVRASSRVSG SFPEDSSKER NLVSWESQTQ PQVQVQDEEI TEDDLRLIHE RESSIRQLEA
181 DIMDINEIFK DLGMMIHEQG DVIDSIEANV ENAEVHVQQA NQQLSRAADY QRKSRKTLCI
241 IILILVIGVA IISLIIWGLN HLocalizationUniProt · AlphaFold · HPA
Whether an antibody against STX7 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 71 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 71 nTPM
- tonsil: 67 nTPM
- kidney: 48 nTPM
- spleen: 43 nTPM
- placenta: 40 nTPM
- appendix: 39 nTPM
Single-cell type
- microglia: 443 nCPM
- neutrophils: 387 nCPM
- hofbauer cells: 365 nCPM
- melanocytes: 364 nCPM
- b-cells: 318 nCPM
- platelets: 285 nCPM
Immune cell
- naive B-cell: 107 nTPM
- memory B-cell: 86 nTPM
- neutrophil: 84 nTPM
- plasmacytoid DC: 74 nTPM
- non-classical monocyte: 62 nTPM
- myeloid DC: 62 nTPM
Brain region
- white matter: 67 nTPM
- medulla oblongata: 56 nTPM
- midbrain: 53 nTPM
- spinal cord: 50 nTPM
- hypothalamus: 50 nTPM
- cerebral cortex: 50 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about STX7.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 48 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.02
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.81
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intracellular protein transport
- organelle assembly
- organelle localization
- positive regulation of receptor localization to synapse
- positive regulation of T cell mediated cytotoxicity
- regulation of protein localization to plasma membrane
- vesicle docking
- vesicle fusion
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of STX7 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads STX7 as an antibody target. Whether an autoantibody or antibody against STX7 could matter depends on whether native STX7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
STX7 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label STX7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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