RIPPLY3
Protein ripply3
Also known as: DSCR6, DSCR6_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P57055
- Gene
- RIPPLY3
- Ensembl
- ENSG00000183145
- Chromosome
- 21
- Canonical length
- 190 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to be involved in embryonic pattern specification and negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of cell population proliferation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
190 residues, UniProt reviewed canonical sequence.
>P57055|RIPPLY3
1 MEPEAAAGAR KARGRGCHCP GDAPWRPPPP RGPESPAPWR PWIQTPGDAE LTRTGRPLEP
61 RADQHTFGSK GAFGFQHPVR VYLPMSKRQE YLRSSGEQVL ASFPVQATID FYDDESTESA
121 SEAEEPEEGP PPLHLLPQEV GGRQENGPGG KGRDQGINQG QRSSGGGDHW GEGPLPQGVS
181 SRGGKCSSSKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RIPPLY3 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)
- 0.62
- Highest tissue expression
- 0.2 nTPM
Expression across tissuesHPA
Tissue
- kidney: 0.2 nTPM
- parathyroid gland: 0.2 nTPM
- basal ganglia: 0.1 nTPM
- cervix: 0.1 nTPM
- esophagus: 0.1 nTPM
- lung: 0.1 nTPM
Single-cell type
- alveolar cells type 1: 6.2 nCPM
- epididymal principal cells: 5.1 nCPM
- retinal pigment epithelial cells: 4.3 nCPM
- pancreatic islet cells: 3.9 nCPM
- extravillous trophoblasts: 3.3 nCPM
- transitional alveolar cells: 3.3 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
- basal ganglia: 1.7 nTPM
- cerebral cortex: 0.5 nTPM
- cerebellum: 0.2 nTPM
- thalamus: 0.2 nTPM
- amygdala: 0.1 nTPM
- hippocampal formation: 0.1 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)
- 1.38
- gnomAD pLI
- 0.08
- gnomAD missense Z
- -0.29
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
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
- cell population proliferation
- embryonic pattern specification
- heart development
- negative regulation of cell population proliferation
- negative regulation of transcription by RNA polymerase II
- pharyngeal system development
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RIPPLY3 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 RIPPLY3 as an antibody target. Whether an autoantibody or antibody against RIPPLY3 could matter depends on whether native RIPPLY3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RIPPLY3 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 RIPPLY3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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