TMEM9
Proton-transporting V-type ATPase complex assembly regulator TMEM9
Also known as: TMEM9_HUMAN, TMEM9A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P0T7
- Gene
- TMEM9
- Ensembl
- ENSG00000116857
- Chromosome
- 1
- Canonical length
- 183 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Vesicles,Microtubules,Cytokinetic bridge,Mitotic spindle
OverviewNCBI Gene
Involved in intracellular pH reduction; positive regulation of canonical Wnt signaling pathway; and proton-transporting V-type ATPase complex assembly. Located in bounding membrane of organelle; intercellular bridge; and mitotic spindle. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
183 residues, UniProt reviewed canonical sequence.
>Q9P0T7|TMEM9
1 MKLLSLVAVV GCLLVPPAEA NKSSEDIRCK CICPPYRNIS GHIYNQNVSQ KDCNCLHVVE
61 PMPVPGHDVE AYCLLCECRY EERSTTTIKV IIVIYLSVVG ALLLYMAFLM LVDPLIRKPD
121 AYTEQLHNEE ENEDARSMAA AAASLGGPRA NTVLERVEGA QQRWKLQVQE QRKTVFDRHK
181 MLSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM9 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)
- 0.47
- Highest tissue expression
- 185 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 185 nTPM
- cerebral cortex: 118 nTPM
- hypothalamus: 113 nTPM
- basal ganglia: 109 nTPM
- amygdala: 107 nTPM
- hippocampal formation: 102 nTPM
Single-cell type
- late spermatids: 213 nCPM
- oocytes: 120 nCPM
- pancreatic islet cells: 97 nCPM
- early spermatids: 96 nCPM
- differentiating spermatogonia: 91 nCPM
- decidual stromal cells: 88 nCPM
Immune cell
- total PBMC: 76 nTPM
- naive CD4 T-cell: 65 nTPM
- classical monocyte: 60 nTPM
- plasmacytoid DC: 56 nTPM
- memory B-cell: 55 nTPM
- MAIT T-cell: 52 nTPM
Brain region
- choroid plexus: 116 nTPM
- hypothalamus: 95 nTPM
- midbrain: 94 nTPM
- thalamus: 86 nTPM
- hippocampal formation: 84 nTPM
- cerebral cortex: 79 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)
- 1.17
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.11
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- endosomal lumen acidification
- lysosomal lumen acidification
- positive regulation of canonical Wnt signaling pathway
- protein transport
- proton-transporting V-type ATPase complex assembly
- regulation of protein catabolic process
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMEM9 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 TMEM9 as an antibody target. Whether an autoantibody or antibody against TMEM9 could matter depends on whether native TMEM9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM9 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 TMEM9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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