Seroatlas · Human Serome Atlas

TMEM270

Transmembrane protein 270

Also known as: MGC26719, TM270_HUMAN, WBSCR28

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q6UE05
Gene
TMEM270
Ensembl
ENSG00000175877
Chromosome
7
Canonical length
265 aa
Protein class
Human disease related genes, Predicted membrane proteins
Subcellular location
Vesicles

OverviewNCBI Gene

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

265 residues, UniProt reviewed canonical sequence.

>Q6UE05|TMEM270
     1  MEALPPVRSS LLGILLQVTR LSVLLVQNRD HLYNFLLLKI NLFNHWVSGL AQEARGSCNW
    61  QAHLPLGAAA CPLGQALWAG LALIQVPVWL VLQGPRLMWA GMWGSTKGLG LALLSAWEQL
   121  GLSVAIWTDL FLSCLHGLML VALLLVVVTW RVCQKSHCFR LGRQLSKALQ VNCVVRKLLV
   181  QLRRLYWWVE TMTALTSWHL AYLITWTTCL ASHLLQAAFE HTTQLAEAQE VEPQEVSGSS
   241  LLPSLSASSD SESGTVLPEQ ETPRE

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against TMEM270 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
Unknown
Secreted
No
Transmembrane segments
3
Mean surface accessibility (rSASA)
0.55
Highest tissue expression
75 nTPM

Expression across tissuesHPA

Tissue

  • testis: 75 nTPM
  • duodenum: 0.3 nTPM
  • pituitary gland: 0.3 nTPM
  • hippocampal formation: 0.2 nTPM
  • hypothalamus: 0.2 nTPM
  • amygdala: 0.1 nTPM

Single-cell type

  • early spermatids: 1,091 nCPM
  • late spermatids: 387 nCPM
  • late primary spermatocytes: 311 nCPM
  • respiratory ciliated cells: 6.1 nCPM
  • sertoli cells: 4.8 nCPM
  • urothelial cells: 4.2 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • amygdala: 0 nTPM
  • basal ganglia: 0 nTPM
  • cerebellum: 0 nTPM
  • cerebral cortex: 0 nTPM
  • choroid plexus: 0 nTPM
  • hippocampal formation: 0 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)
1.64
gnomAD pLI
0
DepMap mean gene effect
-0.14
DepMap dependency class
selective

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

Cellular components

Protein domainsUniProt · Pfam · InterPro

  • Williams-Beuren syndrome chromosomal region 28 protein homologue
  • Williams-Beuren syndrome chromosomal region 28 protein homologue

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads TMEM270 as an antibody target. Whether an autoantibody or antibody against TMEM270 could matter depends on whether native TMEM270 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

TMEM270 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 TMEM270 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/TMEM270. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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