PRRG1
Transmembrane gamma-carboxyglutamic acid protein 1
Also known as: PRGP1, TMG1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O14668
- Gene
- PRRG1
- Ensembl
- ENSG00000130962
- Chromosome
- X
- Canonical length
- 218 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Vesicles,Plasma membrane
OverviewNCBI Gene
This gene encodes a vitamin K-dependent, gamma-carboxyglutamic acid (Gla)-containing, single-pass transmembrane protein. This protein contains a Gla domain at the N-terminus, preceded by a propeptide sequence required for post-translational gamma-carboxylation of specific glutamic acid residues by a vitamin K-dependent gamma-carboxylase. The C-terminus is proline-rich containing PPXY and PXXP motifs found in a variety of signaling and cytoskeletal proteins. This gene is highly expressed in the spinal cord. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]
Canonical amino-acid sequenceUniProt
218 residues, UniProt reviewed canonical sequence.
>O14668|PRRG1
1 MGRVFLTGEK ANSILKRYPR ANGFFEEIRQ GNIERECKEE FCTFEEAREA FENNEKTKEF
61 WSTYTKAQQG ESNRGSDWFQ FYLTFPLIFG LFIILLVIFL IWRCFLRNKT RRQTVTEGHI
121 PFPQHLNIIT PPPPPDEVFD SSGLSPGFLG YVVGRSDSVS TRLSNCDPPP TYEEATGQVN
181 LQRSETEPHL DPPPEYEDIV NSNSASAIPM VPVVTTIKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRRG1 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)
- 0.59
- Highest tissue expression
- 40 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 40 nTPM
- midbrain: 20 nTPM
- skeletal muscle: 15 nTPM
- hippocampal formation: 15 nTPM
- cerebral cortex: 12 nTPM
- basal ganglia: 10 nTPM
Single-cell type
- oligodendrocytes: 235 nCPM
- bergmann glia: 40 nCPM
- myonuclei: 37 nCPM
- vascular endothelial cells: 33 nCPM
- lymphatic endothelial cells: 27 nCPM
- astrocytes: 26 nCPM
Immune cell
- basophil: 0.7 nTPM
- classical monocyte: 0.3 nTPM
- memory B-cell: 0.1 nTPM
- neutrophil: 0.1 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- white matter: 79 nTPM
- medulla oblongata: 56 nTPM
- basal ganglia: 51 nTPM
- cerebellum: 45 nTPM
- pons: 44 nTPM
- midbrain: 44 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)
- 1.12
- gnomAD pLI
- 0.13
- gnomAD missense Z
- 0.41
- DepMap mean gene effect
- 0.13
- 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
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PRRG1 as an antibody target. Whether an autoantibody or antibody against PRRG1 could matter depends on whether native PRRG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRRG1 is annotated at the cell surface, where native PRRG1 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 PRRG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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