SEC22C
Vesicle-trafficking protein SEC22c
Also known as: MGC13261, MGC5373, SC22C_HUMAN, SEC22L3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BRL7
- Gene
- SEC22C
- Ensembl
- ENSG00000093183
- Chromosome
- 3
- Canonical length
- 303 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus
OverviewNCBI Gene
This gene encodes a member of the SEC22 family of vesicle trafficking proteins. The encoded protein is localized to the endoplasmic reticulum and may play a role in the early stages of ER-Golgi protein trafficking. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]
Canonical amino-acid sequenceUniProt
303 residues, UniProt reviewed canonical sequence.
>Q9BRL7|SEC22C
1 MSVIFFACVV RVRDGLPLSA STDFYHTQDF LEWRRRLKSL ALRLAQYPGR GSAEGCDFSI
61 HFSSFGDVAC MAICSCQCPA AMAFCFLETL WWEFTASYDT TCIGLASRPY AFLEFDSIIQ
121 KVKWHFNYVS SSQMECSLEK IQEELKLQPP AVLTLEDTDV ANGVMNGHTP MHLEPAPNFR
181 MEPVTALGIL SLILNIMCAA LNLIRGVHLA EHSLQVAHEE IGNILAFLVP FVACIFQCYL
241 YLFYSPARTM KVVLMLLFIC LGNMYLHGLR NLWQILFHIG VAFLSSYQIL TRQLQEKQSD
301 CGVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SEC22C 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
- 4
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 63 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 63 nTPM
- blood vessel: 43 nTPM
- midbrain: 42 nTPM
- prostate: 35 nTPM
- bone marrow: 34 nTPM
- basal ganglia: 34 nTPM
Single-cell type
- cardiomyocytes: 196 nCPM
- epicardial cells: 134 nCPM
- late primary spermatocytes: 119 nCPM
- mast cells: 91 nCPM
- erythrocyte progenitors: 87 nCPM
- early primary spermatocytes: 79 nCPM
Immune cell
- eosinophil: 22 nTPM
- MAIT T-cell: 20 nTPM
- memory CD4 T-cell: 18 nTPM
- T-reg: 16 nTPM
- memory CD8 T-cell: 16 nTPM
- naive CD4 T-cell: 15 nTPM
Brain region
- white matter: 63 nTPM
- medulla oblongata: 53 nTPM
- pons: 50 nTPM
- basal ganglia: 50 nTPM
- midbrain: 50 nTPM
- cerebellum: 47 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)
- 1.22
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.84
- DepMap mean gene effect
- -0.14
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SEC22C 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 SEC22C as an antibody target. Whether an autoantibody or antibody against SEC22C could matter depends on whether native SEC22C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SEC22C 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 SEC22C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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