TMEM163
Transmembrane protein 163
Also known as: DKFZP566N034, SV31, TM163_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TC26
- Gene
- TMEM163
- Ensembl
- ENSG00000152128
- Chromosome
- 2
- Canonical length
- 289 aa
- Protein class
- Predicted membrane proteins, Transporters
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Predicted to enable zinc ion binding activity. Involved in myelination and zinc export across plasma membrane. Predicted to be located in early endosome membrane. Predicted to be active in plasma membrane and synaptic vesicle membrane. Implicated in hypomyelinating leukodystrophy 25. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
289 residues, UniProt reviewed canonical sequence.
>Q8TC26|TMEM163
1 MEPAAGIQRR SSQGPTVPPP PRGHAPPAAA PGPAPLSSPV REPPQLEEER QVRISESGQF
61 SDGLEDRGLL ESSTRLKPHE AQNYRKKALW VSWFSIIVTL ALAVAAFTVS VMRYSASAFG
121 FAFDAILDVL SSAIVLWRYS NAAAVHSAHR EYIACVILGV IFLLSSICIV VKAIHDLSTR
181 LLPEVDDFLF SVSILSGILC SILAVLKFML GKVLTSRALI TDGFNSLVGG VMGFSILLSA
241 EVFKHDSAVW YLDGSIGVLI GLTIFAYGVK LLIDMVPRVR QTRHYEMFELocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM163 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 6
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 44 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 44 nTPM
- pancreas: 26 nTPM
- spinal cord: 21 nTPM
- hypothalamus: 17 nTPM
- tonsil: 15 nTPM
- cerebral cortex: 14 nTPM
Single-cell type
- pancreatic acinar cells: 1,089 nCPM
- alveolar cells type 2: 950 nCPM
- retinal ganglion cells: 537 nCPM
- gonadotrophs: 536 nCPM
- oocytes: 364 nCPM
- foveolar cells: 353 nCPM
Immune cell
- T-reg: 0.7 nTPM
- memory CD8 T-cell: 0.6 nTPM
- NK-cell: 0.6 nTPM
- MAIT T-cell: 0.4 nTPM
- memory B-cell: 0.4 nTPM
- gdT-cell: 0.3 nTPM
Brain region
- thalamus: 52 nTPM
- white matter: 41 nTPM
- midbrain: 36 nTPM
- medulla oblongata: 32 nTPM
- cerebellum: 31 nTPM
- hypothalamus: 31 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TMEM163.
Disease | AllUniProt
Conditions TMEM163 is implicated in, by any mechanism.
- Leukodystrophy, hypomyelinating, 25 (HLD25) MIM:620243
Disease | GeneticClinVar
4 pathogenic / likely-pathogenic of 60 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Leukodystrophy, hypomyelinating, 25
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)
- 0.85
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 1.77
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intracellular zinc ion homeostasis
- myelination
- zinc export across plasma membrane
- zinc ion import into synaptic vesicle
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cation efflux transmembrane domain superfamily
- Transmembrane protein 163
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMEM163 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 TMEM163 as an antibody target. Whether an autoantibody or antibody against TMEM163 could matter depends on whether native TMEM163 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM163 is annotated at the cell surface, where native TMEM163 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label TMEM163 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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