TMEM151A
Transmembrane protein 151A
Also known as: MGC33486, T151A_HUMAN, TMEM151
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N4L1
- Gene
- TMEM151A
- Ensembl
- ENSG00000179292
- Chromosome
- 11
- Canonical length
- 468 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Nucleoli,Cytosol
OverviewNCBI Gene
Located in endoplasmic reticulum and membrane. Implicated in episodic kinesigenic dyskinesia 3. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
468 residues, UniProt reviewed canonical sequence.
>Q8N4L1|TMEM151A
1 MPEDGAGDGG EVPALIPDGE PLREEQRPLK QSLGSSLCRE SHWKCLLLTL LIHACGAVVA
61 WCRLATVPRL VLGPEAALAR GAGGPPPTYP ASPCSDGYLY IPLAFVSLLY LLYLAECWHC
121 HVRSCQAPRT DAHTVLALIR RLQQAPPCVW WKATSYHYVR RTRQITRYRN GDAYTTTQVY
181 HERADSRTAR GEFDYSAHGV RDVSKELVGL AEHAATRLRF TKCFSFGSAE AEASYLTQRA
241 RFFSANEGLD DYLEAREGMH LKDVDFRESL MVFADPRSPP WYARAWVFWL VSAATLSWPL
301 RVVAAYGTAH VHYQVEKLFG ASSPPPGAVP SGPPLSRVAT VDFTELEWHI CSNRQLVPSY
361 SEAVVMGAGS GAYLRGCQRC RRSVSSNSLP PARPSGPRLP FSRSRLSLGA GGRATPGVFR
421 SLSGGPLGRR GEDTEPLESP PCYEDALYFP VLIVHGDSGC QGDGQGALLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM151A 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
- 2
- Mean surface accessibility (rSASA)
- 0.43
- Highest tissue expression
- 134 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 134 nTPM
- hippocampal formation: 63 nTPM
- midbrain: 59 nTPM
- basal ganglia: 42 nTPM
- cerebral cortex: 41 nTPM
- hypothalamus: 40 nTPM
Single-cell type
- oligodendrocytes: 89 nCPM
- other brain neurons: 23 nCPM
- brain inhibitory neurons: 20 nCPM
- retinal pigment epithelial cells: 17 nCPM
- brain excitatory neurons: 16 nCPM
- mesothelial cells: 9.2 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 227 nTPM
- medulla oblongata: 183 nTPM
- cerebellum: 155 nTPM
- pons: 148 nTPM
- thalamus: 147 nTPM
- midbrain: 143 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TMEM151A.
Disease | AllUniProt
Conditions TMEM151A is implicated in, by any mechanism.
- Episodic kinesigenic dyskinesia 3 (EKD3) MIM:620245
Disease | GeneticClinVar
11 pathogenic / likely-pathogenic of 86 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Episodic kinesigenic dyskinesia 3
- TMEM151A-related disorder
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)
- 0.94
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.67
- DepMap mean gene effect
- -0.04
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TMEM151A as an antibody target. Whether an autoantibody or antibody against TMEM151A could matter depends on whether native TMEM151A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM151A 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 TMEM151A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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