TMEM33
Transmembrane protein 33
Also known as: FLJ10525, Pom33, TMM33_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P57088
- Gene
- TMEM33
- Ensembl
- ENSG00000109133
- Chromosome
- 4
- Canonical length
- 247 aa
- Protein class
- Predicted membrane proteins, Transporters
OverviewNCBI Gene
Involved in positive regulation of endoplasmic reticulum unfolded protein response; regulation of endoplasmic reticulum tubular network organization; and response to endoplasmic reticulum stress. Located in endoplasmic reticulum membrane; melanosome; and nuclear envelope. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
247 residues, UniProt reviewed canonical sequence.
>P57088|TMEM33
1 MADTTPNGPQ GAGAVQFMMT NKLDTAMWLS RLFTVYCSAL FVLPLLGLHE AASFYQRALL
61 ANALTSALRL HQRLPHFQLS RAFLAQALLE DSCHYLLYSL IFVNSYPVTM SIFPVLLFSL
121 LHAATYTKKV LDARGSNSLP LLRSVLDKLS ANQQNILKFI ACNEIFLMPA TVFMLFSGQG
181 SLLQPFIYYR FLTLRYSSRR NPYCRTLFNE LRIVVEHIIM KPACPLFVRR LCLQSIAFIS
241 RLAPTVPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM33 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
- 3
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 37 nTPM
Expression across tissuesHPA
Tissue
- liver: 37 nTPM
- parathyroid gland: 28 nTPM
- epididymis: 24 nTPM
- kidney: 23 nTPM
- thyroid gland: 22 nTPM
- urinary bladder: 20 nTPM
Single-cell type
- neutrophils: 246 nCPM
- syncytiotrophoblasts: 208 nCPM
- esophageal apical cells: 136 nCPM
- retinal pigment epithelial cells: 128 nCPM
- kupffer cells: 116 nCPM
- monocyte progenitors: 112 nCPM
Immune cell
- neutrophil: 43 nTPM
- basophil: 41 nTPM
- non-classical monocyte: 35 nTPM
- classical monocyte: 32 nTPM
- intermediate monocyte: 31 nTPM
- myeloid DC: 23 nTPM
Brain region
- white matter: 65 nTPM
- choroid plexus: 59 nTPM
- medulla oblongata: 57 nTPM
- spinal cord: 54 nTPM
- midbrain: 54 nTPM
- pons: 54 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)
- 0.84
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.79
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- endoplasmic reticulum tubular network organization
- innate immune response
- membrane organization
- positive regulation of IRE1-mediated unfolded protein response
- positive regulation of PERK-mediated unfolded protein response
- regulation of endoplasmic reticulum tubular network organization
- response to endoplasmic reticulum stress
Cellular components
Protein domainsUniProt · Pfam · InterPro
- TMEM33/Pom33 family
- PER33/POM33 transmembrane regulator
- Transmembrane protein 33/Nucleoporin POM33
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMEM33 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 TMEM33 as an antibody target. Whether an autoantibody or antibody against TMEM33 could matter depends on whether native TMEM33 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM33 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 TMEM33 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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