REG3G
Regenerating islet-derived protein 3-gamma
Also known as: LPPM429, PAP1B, REG3G_HUMAN, UNQ429
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6UW15
- Gene
- REG3G
- Ensembl
- ENSG00000143954
- Chromosome
- 2
- Canonical length
- 175 aa
- Protein class
- Predicted secreted proteins
- Subcellular location
- Cytosol
- Secretome location
- Secreted to digestive system
OverviewNCBI Gene
This gene encodes a member of the regenerating islet-derived genes (REG)3 protein family. These proteins are secreted, C-type lectins with a carbohydrate recognition domain and N-terminal signal peptide. The protein encoded by this gene is an antimicrobial lectin with activity against Gram-positive bacteria. Alternative splicing results in multiple transcript variants encoding multiple isoforms. [provided by RefSeq, Nov 2014]
Canonical amino-acid sequenceUniProt
175 residues, UniProt reviewed canonical sequence.
>Q6UW15|REG3G
1 MLPPMALPSV SWMLLSCLIL LCQVQGEETQ KELPSPRISC PKGSKAYGSP CYALFLSPKS
61 WMDADLACQK RPSGKLVSVL SGAEGSFVSS LVRSISNSYS YIWIGLHDPT QGSEPDGDGW
121 EWSSTDVMNY FAWEKNPSTI LNPGHCGSLS RSTGFLKWKD YNCDAKLPYV CKFKDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against REG3G 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)
- 0.36
- Highest tissue expression
- 3,450 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 3,450 nTPM
- epididymis: 156 nTPM
- testis: 59 nTPM
- adrenal gland: 43 nTPM
- small intestine: 37 nTPM
- kidney: 6.8 nTPM
Single-cell type
- pancreatic acinar cells: 7,001 nCPM
- sertoli cells: 103 nCPM
- epididymal principal cells: 66 nCPM
- enterocytes: 38 nCPM
- paneth cells: 27 nCPM
- granulosa cells: 15 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)
- 1.77
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.93
- DepMap mean gene effect
- 0.19
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 1% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- acute-phase response
- antimicrobial humoral immune response mediated by antimicrobial peptide
- defense response to Gram-positive bacterium
- MyD88-dependent toll-like receptor signaling pathway
- negative regulation of keratinocyte differentiation
- positive regulation of cell population proliferation
- positive regulation of keratinocyte proliferation
- positive regulation of wound healing
- response to peptide hormone
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of REG3G 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 REG3G as an antibody target. Whether an autoantibody or antibody against REG3G could matter depends on whether native REG3G is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
REG3G is annotated as secreted, so native REG3G 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 REG3G as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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