TMED9
Transmembrane emp24 domain-containing protein 9
Also known as: HSGP25L2G, p24a2, p24alpha2, TMED9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BVK6
- Gene
- TMED9
- Ensembl
- ENSG00000184840
- Chromosome
- 5
- Canonical length
- 235 aa
- Protein class
- Predicted membrane proteins, Transporters
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene is a member of a family of genes encoding transport proteins located in the endoplasmic reticulum and the Golgi. A similar gene in mouse is the target of microRNA miR-296, which is part of an imprinted cluster. [provided by RefSeq, Jul 2016]
Canonical amino-acid sequenceUniProt
235 residues, UniProt reviewed canonical sequence.
>Q9BVK6|TMED9
1 MAVELGVLLV RPRPGTGLGR VMRTLLLVLW LATRGSALYF HIGETEKKCF IEEIPDETMV
61 IGNYRTQLYD KQREEYQPAT PGLGMFVEVK DPEDKVILAR QYGSEGRFTF TSHTPGEHQI
121 CLHSNSTKFS LFAGGMLRVH LDIQVGEHAN DYAEIAAKDK LSELQLRVRQ LVEQVEQIQK
181 EQNYQRWREE RFRQTSESTN QRVLWWSILQ TLILVAIGVW QMRHLKSFFE AKKLVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMED9 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)
- 0.41
- Highest tissue expression
- 96 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 96 nTPM
- choroid plexus: 90 nTPM
- liver: 89 nTPM
- salivary gland: 73 nTPM
- epididymis: 62 nTPM
- placenta: 56 nTPM
Single-cell type
- extravillous trophoblasts: 1,278 nCPM
- syncytiotrophoblasts: 1,002 nCPM
- migrating cytotrophoblasts: 637 nCPM
- esophageal apical cells: 625 nCPM
- cytotrophoblasts: 609 nCPM
- epididymal principal cells: 503 nCPM
Immune cell
- plasmacytoid DC: 202 nTPM
- total PBMC: 132 nTPM
- classical monocyte: 98 nTPM
- intermediate monocyte: 95 nTPM
- myeloid DC: 92 nTPM
- non-classical monocyte: 89 nTPM
Brain region
- choroid plexus: 42 nTPM
- thalamus: 22 nTPM
- medulla oblongata: 22 nTPM
- midbrain: 19 nTPM
- spinal cord: 19 nTPM
- pons: 18 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)
- 0.82
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.93
- DepMap mean gene effect
- -0.07
- 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
Biological processes
- COPI coating of Golgi vesicle
- endoplasmic reticulum to Golgi vesicle-mediated transport
- Golgi organization
- intracellular protein transport
- positive regulation of organelle organization
Molecular functions
Cellular components
- COPII-coated ER to Golgi transport vesicle
- endoplasmic reticulum
- endoplasmic reticulum membrane
- endoplasmic reticulum-Golgi intermediate compartment
- endoplasmic reticulum-Golgi intermediate compartment membrane
- extracellular exosome
- Golgi apparatus
- Golgi membrane
- synaptic vesicle
- trans-Golgi network transport vesicle
- transport vesicle
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMED9 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 TMED9 as an antibody target. Whether an autoantibody or antibody against TMED9 could matter depends on whether native TMED9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMED9 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 TMED9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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