RIC8A
Chaperone Ric-8A
Also known as: RIC8A_HUMAN, synembryn, synembryn-A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NPQ8
- Gene
- RIC8A
- Ensembl
- ENSG00000177963
- Chromosome
- 11
- Canonical length
- 531 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
Predicted to enable G-protein alpha-subunit binding activity; GTPase regulator activity; and protein folding chaperone. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to act upstream of or within several processes, including basement membrane organization; gastrulation; and visual learning. Predicted to be located in cell cortex and membrane. Predicted to be active in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
531 residues, UniProt reviewed canonical sequence.
>Q9NPQ8|RIC8A
1 MEPRAVAEAV ETGEEDVIME ALRSYNQEHS QSFTFDDAQQ EDRKRLAELL VSVLEQGLPP
61 SHRVIWLQSV RILSRDRNCL DPFTSRQSLQ ALACYADISV SEGSVPESAD MDVVLESLKC
121 LCNLVLSSPV AQMLAAEARL VVKLTERVGL YRERSFPHDV QFFDLRLLFL LTALRTDVRQ
181 QLFQELKGVR LLTDTLELTL GVTPEGNPPP TLLPSQETER AMEILKVLFN ITLDSIKGEV
241 DEEDAALYRH LGTLLRHCVM IATAGDRTEE FHGHAVNLLG NLPLKCLDVL LTLEPHGDST
301 EFMGVNMDVI RALLIFLEKR LHKTHRLKES VAPVLSVLTE CARMHRPARK FLKAQVLPPL
361 RDVRTRPEVG EMLRNKLVRL MTHLDTDVKR VAAEFLFVLC SESVPRFIKY TGYGNAAGLL
421 AARGLMAGGR PEGQYSEDED TDTDEYKEAK ASINPVTGRV EEKPPNPMEG MTEEQKEHEA
481 MKLVTMFDKL SRNRVIQPMG MSPRGHLTSL QDAMCETMEQ QLSSDPDSDP DLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RIC8A 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)
- 0.28
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 49 nTPM
- smooth muscle: 46 nTPM
- blood vessel: 44 nTPM
- colon: 43 nTPM
- endometrium: 42 nTPM
- urinary bladder: 42 nTPM
Single-cell type
- late primary spermatocytes: 97 nCPM
- early primary spermatocytes: 92 nCPM
- extravillous trophoblasts: 76 nCPM
- hofbauer cells: 61 nCPM
- alveolar cells type 1: 61 nCPM
- migrating cytotrophoblasts: 60 nCPM
Immune cell
- eosinophil: 89 nTPM
- total PBMC: 87 nTPM
- gdT-cell: 79 nTPM
- MAIT T-cell: 78 nTPM
- NK-cell: 73 nTPM
- basophil: 72 nTPM
Brain region
- choroid plexus: 45 nTPM
- cerebral cortex: 43 nTPM
- hippocampal formation: 42 nTPM
- midbrain: 41 nTPM
- white matter: 41 nTPM
- thalamus: 40 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)
- 0.73
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.83
- DepMap mean gene effect
- 0.02
- 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
- adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
- basement membrane organization
- cell migration involved in gastrulation
- G protein-coupled receptor signaling pathway
- in utero embryonic development
- vasculature development
- visual learning
- cell-cell adhesion involved in gastrulation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RIC8A 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 RIC8A as an antibody target. Whether an autoantibody or antibody against RIC8A could matter depends on whether native RIC8A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RIC8A 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 RIC8A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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