PRR7
Proline-rich protein 7
Also known as: MGC10772, PRR7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TB68
- Gene
- PRR7
- Ensembl
- ENSG00000131188
- Chromosome
- 5
- Canonical length
- 274 aa
- Protein class
- Predicted intracellular proteins, Transporters
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
OverviewNCBI Gene
Enables long-chain fatty acid binding activity; protein tyrosine kinase binding activity; and ubiquitin-like protein ligase binding activity. Involved in positive regulation of apoptotic process and regulation of transcription by RNA polymerase I. Located in several cellular components, including cytosol; nucleoplasm; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
274 residues, UniProt reviewed canonical sequence.
>Q8TB68|PRR7
1 MVMSQGTYTF LTCFAGFWLI WGLIVLLCCF CSFLRRRLKR RQEERLREQN LRALELEPLE
61 LEGSLAGSPP GLAPPQPPPH RSRLEAPAHA HSHPHVHVHP LLHHGPAQPH AHAHPHPHHH
121 ALPHPPPTHL SVPPRPWSYP RQAESDMSKP PCYEEAVLMA EPPPPYSEVL TDTRGLYRKI
181 VTPFLSRRDS AEKQEQPPPS YKPLFLDRGY TSALHLPSAP RPAPPCPALC LQADRGRRVF
241 PSWTDSELSS REPLEHGAWR LPVSIPLFGR TTAVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRR7 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
- 1
- Mean surface accessibility (rSASA)
- 0.67
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 32 nTPM
- hippocampal formation: 28 nTPM
- amygdala: 21 nTPM
- cerebral cortex: 19 nTPM
- hypothalamus: 14 nTPM
- pituitary gland: 10 nTPM
Single-cell type
- megakaryocytes: 124 nCPM
- fallopian tube ciliated cells: 68 nCPM
- respiratory ciliated cells: 64 nCPM
- platelets: 61 nCPM
- suprabasal keratinocytes: 46 nCPM
- epididymal efferent duct ciliated cells: 46 nCPM
Immune cell
- eosinophil: 9.7 nTPM
- MAIT T-cell: 5.5 nTPM
- memory CD8 T-cell: 3.9 nTPM
- neutrophil: 3.7 nTPM
- naive CD8 T-cell: 3.1 nTPM
- naive B-cell: 2.8 nTPM
Brain region
- cerebral cortex: 55 nTPM
- hippocampal formation: 54 nTPM
- basal ganglia: 42 nTPM
- amygdala: 39 nTPM
- hypothalamus: 32 nTPM
- choroid plexus: 30 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)
- 0.45
- gnomAD pLI
- 0.87
- gnomAD missense Z
- 1.29
- DepMap mean gene effect
- -0.22
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adaptive immune response
- alpha-beta T cell differentiation
- positive regulation of apoptotic process
- postsynapse to nucleus signaling pathway
- regulation of transcription by RNA polymerase I
- T cell differentiation in thymus
Molecular functions
- long-chain fatty acid binding
- protein tyrosine kinase binding
- protein-containing complex binding
- ubiquitin-like protein ligase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PRR7 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 PRR7 as an antibody target. Whether an autoantibody or antibody against PRR7 could matter depends on whether native PRR7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRR7 is annotated at the cell surface, where native PRR7 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 PRR7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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