RPH3AL
Rab effector Noc2
Also known as: Noc2, RPH3L_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UNE2
- Gene
- RPH3AL
- Ensembl
- ENSG00000181031
- Chromosome
- 17
- Canonical length
- 315 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene plays a direct regulatory role in calcium-ion-dependent exocytosis in both endocrine and exocrine cells and plays a key role in insulin secretion by pancreatic cells. This gene is likely a tumor suppressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jun 2010]
Canonical amino-acid sequenceUniProt
315 residues, UniProt reviewed canonical sequence.
>Q9UNE2|RPH3AL
1 MADTIFGSGN DQWVCPNDRQ LALRAKLQTG WSVHTYQTEK QRRKQHLSPA EVEAILQVIQ
61 RAERLDVLEQ QRIGRLVERL ETMRRNVMGN GLSQCLLCGE VLGFLGSSSV FCKDCRKKVC
121 TKCGIEASPG QKRPLWLCKI CSEQREVWKR SGAWFYKGLP KYILPLKTPG RADDPHFRPL
181 PTEPAEREPR SSETSRIYTW ARGRVVSSDS DSDSDLSSSS LEDRLPSTGV RDRKGDKPWK
241 ESGGSVEAPR MGFTHPPGHL SGCQSSLASG ETGTGSADPP GGPRPGLTRR APVKDTPGRA
301 PAADAAPAGP SSCLGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RPH3AL 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)
- 0.55
- Highest tissue expression
- 50 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 50 nTPM
- pituitary gland: 42 nTPM
- liver: 23 nTPM
- adrenal gland: 17 nTPM
- spleen: 17 nTPM
- kidney: 14 nTPM
Single-cell type
- renal collecting duct principal cells: 151 nCPM
- renal connecting tubule cells: 138 nCPM
- papillary tip epithelial cells: 91 nCPM
- renal collecting duct intercalated cells: 82 nCPM
- podocytes: 74 nCPM
- loop of henle epithelial cells: 63 nCPM
Immune cell
- plasmacytoid DC: 2.8 nTPM
- intermediate monocyte: 2.2 nTPM
- non-classical monocyte: 1.8 nTPM
- neutrophil: 1.6 nTPM
- eosinophil: 1.5 nTPM
- myeloid DC: 1.1 nTPM
Brain region
- pons: 10 nTPM
- cerebellum: 7.8 nTPM
- medulla oblongata: 7.6 nTPM
- hypothalamus: 5.3 nTPM
- midbrain: 4.8 nTPM
- white matter: 4.4 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)
- 1.41
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.31
- DepMap mean gene effect
- 0.1
- 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
- calcium-dependent activation of synaptic vesicle fusion
- exocytosis
- G protein-coupled receptor signaling pathway
- glucose homeostasis
- intracellular protein transport
- negative regulation of G protein-coupled receptor signaling pathway
- positive regulation of calcium ion-dependent exocytosis
- positive regulation of insulin secretion
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RPH3AL 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 RPH3AL as an antibody target. Whether an autoantibody or antibody against RPH3AL could matter depends on whether native RPH3AL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RPH3AL 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 RPH3AL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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