TMEM123

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Porimin is a protein that in humans is encoded by the TMEM123 gene.[5][6]

AliasesTMEM123, KCT3, PORIMIN, PORMIN, transmembrane protein 123
End102,470,384 bp[1]
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TMEM123
Identifiers
AliasesTMEM123, KCT3, PORIMIN, PORMIN, transmembrane protein 123
External IDsOMIM: 606356; MGI: 1919179; HomoloGene: 14177; GeneCards: TMEM123; OMA:TMEM123 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_052932

NM_133739

RefSeq (protein)

NP_443164

NP_598500

Location (UCSC)Chr 11: 102.4 – 102.47 MbChr 9: 7.76 – 7.79 Mb
PubMed search[3][4]
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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.[6]

References

Further reading

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