Seroatlas · Human Serome Atlas

TMEM186

Transmembrane protein 186

Also known as: C16orf51, DKFZP564K2062, TM186_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q96B77
Gene
TMEM186
Ensembl
ENSG00000184857
Chromosome
16
Canonical length
213 aa
Protein class
Predicted membrane proteins
Subcellular location
Cell Junctions

OverviewNCBI Gene

This gene encodes a potential transmembrane protein. [provided by RefSeq, Dec 2012]

Canonical amino-acid sequenceUniProt

213 residues, UniProt reviewed canonical sequence.

>Q96B77|TMEM186
     1  MAALLRAVRR FRGKAVWERP LHGLWCCSGQ EDPKRWVGSS SPISKEKLPN AETEKFWMFY
    61  RFDAIRTFGF LSRLKLAQTA LTVVALPPGY YLYSQGLLTL NTVCLMSGIS GFALTMLCWM
   121  SYFLRRLVGI LYLNESGTML RVAHLNFWGW RQDTYCPMAD VIPLTETKDR PQEMFVRIQR
   181  YSGKQTFYVT LRYGRILDRE RFTQVFGVHQ MLK

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against TMEM186 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
2
Mean surface accessibility (rSASA)
0.45
Highest tissue expression
20 nTPM

Expression across tissuesHPA

Tissue

  • tongue: 20 nTPM
  • skeletal muscle: 18 nTPM
  • liver: 16 nTPM
  • choroid plexus: 13 nTPM
  • heart muscle: 13 nTPM
  • epididymis: 12 nTPM

Single-cell type

  • late spermatids: 190 nCPM
  • late primary spermatocytes: 56 nCPM
  • early spermatids: 45 nCPM
  • cytotrophoblasts: 28 nCPM
  • esophageal basal cells: 25 nCPM
  • migrating cytotrophoblasts: 23 nCPM

Immune cell

  • naive CD4 T-cell: 14 nTPM
  • non-classical monocyte: 13 nTPM
  • memory B-cell: 13 nTPM
  • T-reg: 12 nTPM
  • naive B-cell: 12 nTPM
  • naive CD8 T-cell: 11 nTPM

Brain region

  • choroid plexus: 7.1 nTPM
  • white matter: 6.8 nTPM
  • basal ganglia: 6.4 nTPM
  • thalamus: 6.4 nTPM
  • hypothalamus: 6.3 nTPM
  • pons: 6.2 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)
1.58
gnomAD pLI
0
gnomAD missense Z
-1.25
DepMap mean gene effect
-0.05
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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 TMEM186 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 TMEM186 as an antibody target. Whether an autoantibody or antibody against TMEM186 could matter depends on whether native TMEM186 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

TMEM186 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 TMEM186 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/TMEM186. 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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