TMEM123
Porimin
Also known as: KCT3, PORIM_HUMAN, PORIMIN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N131
- Gene
- TMEM123
- Ensembl
- ENSG00000152558
- Chromosome
- 11
- Canonical length
- 208 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Golgi apparatus,Vesicles,Cytosol
OverviewNCBI Gene
This gene encodes a highly glycosylated transmembrane protein with a high content of threonine and serine residues in its extracellular domain, similar to a broadly defined category of proteins termed mucins. Exposure of some cell types to anti-PORIMIN (pro-oncosis receptor inducing membrane injury) antibody, crosslinks this protein on the cell surface and induces a type of cell death termed oncosis. Oncosis is distinct from apoptosis and is characterized by a loss of cell membrane integrity without DNA fragmentation. This gene product is proposed to function as a cell surface receptor that mediates cell death. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
208 residues, UniProt reviewed canonical sequence.
>Q8N131|TMEM123
1 MGLGARGAWA ALLLGTLQVL ALLGAAHESA AMAASANIEN SGLPHNSSAN STETLQHVPS
61 DHTNETSNST VKPPTSVASD SSNTTVTTMK PTAASNTTTP GMVSTNMTST TLKSTPKTTS
121 VSQNTSQIST STMTVTHNSS VTSAASSVTI TTTMHSEAKK GSKFDTGSFV GGIVLTLGVL
181 SILYIGCKMY YSRRGIRYRT IDEHDAIILocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM123 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.66
- Highest tissue expression
- 368 nTPM
Expression across tissuesHPA
Tissue
- liver: 368 nTPM
- thyroid gland: 292 nTPM
- thymus: 222 nTPM
- bone marrow: 213 nTPM
- salivary gland: 211 nTPM
- lymph node: 183 nTPM
Single-cell type
- kupffer cells: 489 nCPM
- lacrimal acinar cells: 447 nCPM
- neutrophil progenitors: 421 nCPM
- monocytes: 408 nCPM
- salivary acinar cells: 358 nCPM
- epididymal efferent duct ciliated cells: 340 nCPM
Immune cell
- total PBMC: 249 nTPM
- NK-cell: 225 nTPM
- naive CD4 T-cell: 209 nTPM
- eosinophil: 208 nTPM
- T-reg: 184 nTPM
- naive CD8 T-cell: 182 nTPM
Brain region
- white matter: 163 nTPM
- medulla oblongata: 131 nTPM
- midbrain: 126 nTPM
- choroid plexus: 121 nTPM
- spinal cord: 110 nTPM
- hypothalamus: 108 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)
- 0.62
- gnomAD pLI
- 0.65
- gnomAD missense Z
- -0.51
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TMEM123 as an antibody target. Whether an autoantibody or antibody against TMEM123 could matter depends on whether native TMEM123 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM123 is annotated at the cell surface, where native TMEM123 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Source-annotated serology context
The source annotations explicitly mention antibody, autoantibody, autoantigen, or autoimmune context. This is biological context, not study-specific reactivity.
- Exposure of some cell types to anti-PORIMIN (pro-oncosis receptor inducing membrane injury) antibody, crosslinks this protein on the cell surface and induces a type of cell death termed oncosis.
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