TMED4
Transmembrane emp24 domain-containing protein 4
Also known as: HNLF, p24a3, p24alpha3, TMED4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z7H5
- Gene
- TMED4
- Ensembl
- ENSG00000158604
- Chromosome
- 7
- Canonical length
- 227 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
Involved in positive regulation of canonical NF-kappaB signal transduction. Predicted to be located in endoplasmic reticulum membrane. Predicted to be active in several cellular components, including COPII-coated ER to Golgi transport vesicle; Golgi apparatus; and endoplasmic reticulum-Golgi intermediate compartment. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
227 residues, UniProt reviewed canonical sequence.
>Q7Z7H5|TMED4
1 MAGVGAGPLR AMGRQALLLL ALCATGAQGL YFHIGETEKR CFIEEIPDET MVIGNYRTQM
61 WDKQKEVFLP STPGLGMHVE VKDPDGKVVL SRQYGSEGRF TFTSHTPGDH QICLHSNSTR
121 MALFAGGKLR VHLDIQVGEH ANNYPEIAAK DKLTELQLRA RQLLDQVEQI QKEQDYQRYR
181 EERFRLTSES TNQRVLWWSI AQTVILILTG IWQMRHLKSF FEAKKLVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMED4 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
- 1
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 131 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 131 nTPM
- thyroid gland: 107 nTPM
- small intestine: 87 nTPM
- retina: 85 nTPM
- duodenum: 83 nTPM
- kidney: 82 nTPM
Single-cell type
- enterocytes: 241 nCPM
- cytotrophoblasts: 206 nCPM
- fallopian tube ciliated cells: 195 nCPM
- syncytiotrophoblasts: 187 nCPM
- plasma cells: 176 nCPM
- lacrimal acinar cells: 161 nCPM
Immune cell
- plasmacytoid DC: 120 nTPM
- MAIT T-cell: 103 nTPM
- basophil: 95 nTPM
- eosinophil: 87 nTPM
- gdT-cell: 85 nTPM
- memory CD4 T-cell: 85 nTPM
Brain region
- white matter: 86 nTPM
- choroid plexus: 84 nTPM
- hypothalamus: 73 nTPM
- medulla oblongata: 72 nTPM
- basal ganglia: 71 nTPM
- midbrain: 66 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TMED4.
Disease | ImmuneIEDB
Conditions an epitope on TMED4 was assayed in.
- chronic lymphocytic leukemia T cell
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)
- 0.66
- gnomAD pLI
- 0.24
- gnomAD missense Z
- 0.74
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 11% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- endoplasmic reticulum to Golgi vesicle-mediated transport
- Golgi organization
- intracellular protein transport
- positive regulation of canonical NF-kappaB signal transduction
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMED4 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 TMED4 as an antibody target. Whether an autoantibody or antibody against TMED4 could matter depends on whether native TMED4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMED4 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 TMED4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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