RYBP
RING1 and YY1-binding protein
Also known as: AAP1, DEDAF, RYBP_HUMAN, YEAF1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N488
- Gene
- RYBP
- Ensembl
- ENSG00000163602
- Chromosome
- 3
- Canonical length
- 228 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables nucleic acid binding activity. Involved in chromatin remodeling; positive regulation of apoptotic process; and regulation of primary metabolic process. Located in nucleoplasm. Part of PcG protein complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
228 residues, UniProt reviewed canonical sequence.
>Q8N488|RYBP
1 MTMGDKKSPT RPKRQAKPAA DEGFWDCSVC TFRNSAEAFK CSICDVRKGT STRKPRINSQ
61 LVAQQVAQQY ATPPPPKKEK KEKVEKQDKE KPEKDKEISP SVTKKNTNKK TKPKSDILKD
121 PPSEANSIQS ANATTKTSET NHTSRPRLKN VDRSTAQQLA VTVGNVTVII TDFKEKTRSS
181 STSSSTVTSS AGSEQQNQSS SGSESTDKGS SRSSTPKGDM SAVNDESFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RYBP 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)
- 0.64
- Highest tissue expression
- 2.5 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 2.5 nTPM
- placenta: 2 nTPM
- retina: 1.9 nTPM
- hippocampal formation: 1.8 nTPM
- amygdala: 1.6 nTPM
- basal ganglia: 1.6 nTPM
Single-cell type
- oligodendrocytes: 592 nCPM
- platelets: 158 nCPM
- distal convoluted tubule cells: 115 nCPM
- renal collecting duct principal cells: 110 nCPM
- renal connecting tubule cells: 109 nCPM
- papillary tip epithelial cells: 105 nCPM
Immune cell
- neutrophil: 0.8 nTPM
- eosinophil: 0.4 nTPM
- intermediate monocyte: 0.2 nTPM
- naive CD4 T-cell: 0.2 nTPM
- non-classical monocyte: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
Brain region
- cerebral cortex: 4.1 nTPM
- hypothalamus: 4.1 nTPM
- white matter: 3.6 nTPM
- basal ganglia: 3.5 nTPM
- hippocampal formation: 3.2 nTPM
- amygdala: 2.8 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)
- 0.72
- gnomAD pLI
- 0.18
- gnomAD missense Z
- 0.66
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
- apoptotic process
- chromatin remodeling
- negative regulation of proteasomal ubiquitin-dependent protein catabolic process
- negative regulation of transcription by RNA polymerase II
- positive regulation of apoptotic process
- positive regulation of DNA-templated transcription
- regulation of DNA-templated transcription
Molecular functions
- DNA binding
- nucleic acid binding
- transcription coregulator activity
- transcription corepressor activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RYBP 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 RYBP as an antibody target. Whether an autoantibody or antibody against RYBP could matter depends on whether native RYBP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RYBP 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 RYBP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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