PRAMEF18
PRAME family member 18
Also known as: PRA18_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5VWM3
- Gene
- PRAMEF18
- Ensembl
- ENSG00000279804
- Chromosome
- 1
- Canonical length
- 479 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable ubiquitin-like ligase-substrate adaptor activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be part of Cul2-RING ubiquitin ligase complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
479 residues, UniProt reviewed canonical sequence.
>Q5VWM3|PRAMEF18
1 MSFQAPRRLL ELAGQSLLRD QALAISVLDE LPRELFPPLF VEAFTSRRCE VLKVMVQAWP
61 FPCLPLGSLM KTPDLEILHY VVDGIDCLLA QKVRPRRWKL QVLEMRDVDE NFWTIWSGAR
121 LLSCSPEAMS KRQTVEDCPR TGEKQPLKVF MDVCLKEKFM DEDLSFFSGW VQHRRGSVHL
181 CCTKVVNYSM SILNFRNILE TVYPDSIQVL EIWNMCWLCM IVEFSRYLSQ MRNLRKLFIS
241 DGCRYLLSSD SQEQLVAEFS SVLLRLENLQ MLYVRRVCFF RGHLDQLIRC LRSPLETLAL
301 TYGFLEEEDL KCLPRYPSLS QLKQLNLSHG ALRFIRLEPL RALLEKVAAT LQTLFLVDCG
361 IGYSKLRVIL PALSRCSNLT TFCFHGNDTS MDALKDLLRH TGRLSNLSLE TYPAPRESLD
421 NRGRVILELL TPLQAELMRI LREVREPKRI FFGPVSCPCC GTSPTEQLES NFCLWGRPALocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRAMEF18 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 0.1 nTPM
Expression across tissuesHPA
Tissue
- testis: 0.1 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
- amygdala: 0 nTPM
- appendix: 0 nTPM
- basal ganglia: 0 nTPM
Single-cell type
- adipocytes: 0 nCPM
- adrenal cortex cells: 0 nCPM
- adrenal medulla cells: 0 nCPM
- alveolar cells type 1: 0 nCPM
- alveolar cells type 2: 0 nCPM
- astrocytes: 0 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
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 1.88
- gnomAD pLI
- 0.3
- gnomAD missense Z
- -0.8
- DepMap mean gene effect
- -0.23
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 0% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of apoptotic process
- negative regulation of cell differentiation
- negative regulation of DNA-templated transcription
- positive regulation of cell population proliferation
- proteasome-mediated ubiquitin-dependent protein catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PRAMEF18 as an antibody target. Whether an autoantibody or antibody against PRAMEF18 could matter depends on whether native PRAMEF18 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRAMEF18 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 PRAMEF18 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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