PDGFRL
Platelet-derived growth factor receptor-like protein
Also known as: PGFRL_HUMAN, PRLTS
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15198
- Gene
- PDGFRL
- Ensembl
- ENSG00000104213
- Chromosome
- 8
- Canonical length
- 375 aa
- Protein class
- Disease related genes, Potential drug targets, Predicted secreted proteins, Transporters
- Subcellular location
- Nucleoplasm,Nucleoli,Golgi apparatus
- Secretome location
- Secreted - unknown location
OverviewNCBI Gene
This gene encodes a protein with significant sequence similarity to the ligand binding domain of platelet-derived growth factor receptor beta. Mutations in this gene, or deletion of a chromosomal segment containing this gene, are associated with sporadic hepatocellular carcinomas, colorectal cancers, and non-small cell lung cancers. This suggests this gene product may function as a tumor suppressor. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
375 residues, UniProt reviewed canonical sequence.
>Q15198|PDGFRL
1 MKVWLLLGLL LVHEALEDVT GQHLPKNKRP KEPGENRIKP TNKKVKPKIP KMKDRDSANS
61 APKTQSIMMQ VLDKGRFQKP AATLSLLAGQ TVELRCKGSR IGWSYPAYLD TFKDSRLSVK
121 QNERYGQLTL VNSTSADTGE FSCWVQLCSG YICRKDEAKT GSTYIFFTEK GELFVPSPSY
181 FDVVYLNPDR QAVVPCRVTV LSAKVTLHRE FPAKEIPANG TDIVYDMKRG FVYLQPHSEH
241 QGVVYCRAEA GGRSQISVKY QLLYVAVPSG PPSTTILASS NKVKSGDDIS VLCTVLGEPD
301 VEVEFTWIFP GQKDERPVTI QDTWRLIHRG LGHTTRISQS VITVEDFETI DAGYYICTAQ
361 NLQGQTTVAT TVEFSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PDGFRL 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 62 nTPM
Expression across tissuesHPA
Tissue
- ovary: 62 nTPM
- breast: 50 nTPM
- adipose tissue: 37 nTPM
- tongue: 35 nTPM
- thyroid gland: 31 nTPM
- cervix: 26 nTPM
Single-cell type
- oocytes: 318 nCPM
- fibroblasts: 142 nCPM
- fibro-adipogenic progenitors: 108 nCPM
- leydig cells: 76 nCPM
- cardiomyocytes: 71 nCPM
- peritubular myoid cells: 70 nCPM
Immune cell
- classical monocyte: 0.3 nTPM
- neutrophil: 0.2 nTPM
- myeloid DC: 0.1 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- basal ganglia: 5.4 nTPM
- white matter: 4.8 nTPM
- hypothalamus: 4.2 nTPM
- cerebellum: 4.1 nTPM
- thalamus: 4 nTPM
- medulla oblongata: 3.9 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PDGFRL.
Disease | AllUniProt
Conditions PDGFRL is implicated in, by any mechanism.
- Colorectal cancer (CRC) MIM:114500
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 104 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 1.8
- gnomAD pLI
- 0
- gnomAD missense Z
- -2
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PDGFRL as an antibody target. Whether an autoantibody or antibody against PDGFRL could matter depends on whether native PDGFRL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PDGFRL is annotated as secreted, so native PDGFRL circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label PDGFRL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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