STX12
Syntaxin-12
Also known as: STX12_HUMAN, STX13, STX14
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86Y82
- Gene
- STX12
- Ensembl
- ENSG00000117758
- Chromosome
- 1
- Canonical length
- 276 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus,Vesicles
OverviewNCBI Gene
Predicted to enable SNAP receptor activity and SNARE binding activity. Involved in autophagosome assembly; cholesterol efflux; and protein stabilization. Located in several cellular components, including BLOC-1 complex; phagocytic vesicle; and phagophore assembly site. Part of SNARE complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
276 residues, UniProt reviewed canonical sequence.
>Q86Y82|STX12
1 MSYGPLDMYR NPGPSGPQLR DFSSIIQTCS GNIQRISQAT AQIKNLMSQL GTKQDSSKLQ
61 ENLQQLQHST NQLAKETNEL LKELGSLPLP LSTSEQRQQR LQKERLMNDF SAALNNFQAV
121 QRRVSEKEKE SIARARAGSR LSAEERQREE QLVSFDSHEE WNQMQSQEDE VAITEQDLEL
181 IKERETAIRQ LEADILDVNQ IFKDLAMMIH DQGDLIDSIE ANVESSEVHV ERATEQLQRA
241 AYYQKKSRKK MCILVLVLSV IILILGLIIW LVYKTKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against STX12 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
- 89 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 89 nTPM
- stomach: 62 nTPM
- adipose tissue: 60 nTPM
- epididymis: 59 nTPM
- spinal cord: 54 nTPM
- midbrain: 51 nTPM
Single-cell type
- parietal cells: 438 nCPM
- esophageal apical cells: 387 nCPM
- epididymal basal cells: 381 nCPM
- epididymal principal cells: 351 nCPM
- suprabasal keratinocytes: 267 nCPM
- alveolar cells type 1: 257 nCPM
Immune cell
- non-classical monocyte: 41 nTPM
- intermediate monocyte: 40 nTPM
- classical monocyte: 36 nTPM
- myeloid DC: 25 nTPM
- basophil: 25 nTPM
- total PBMC: 17 nTPM
Brain region
- midbrain: 77 nTPM
- white matter: 75 nTPM
- pons: 74 nTPM
- medulla oblongata: 71 nTPM
- spinal cord: 70 nTPM
- hypothalamus: 69 nTPM
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)
- 0.34
- gnomAD pLI
- 0.96
- gnomAD missense Z
- 0.95
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
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
- autophagosome assembly
- cholesterol efflux
- endocytic recycling
- intracellular protein transport
- protein stabilization
- vesicle docking
- vesicle fusion
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of STX12 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 STX12 as an antibody target. Whether an autoantibody or antibody against STX12 could matter depends on whether native STX12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
STX12 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 STX12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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