RNF186
E3 ubiquitin-protein ligase RNF186
Also known as: FLJ20225, RN186_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NXI6
- Gene
- RNF186
- Ensembl
- ENSG00000178828
- Chromosome
- 1
- Canonical length
- 227 aa
- Protein class
- Enzymes, Predicted membrane proteins
OverviewNCBI Gene
Enables ubiquitin protein ligase activity and ubiquitin protein ligase binding activity. Involved in several processes, including intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein ubiquitination. Acts upstream of with a positive effect on regulation of autophagosome assembly. Located in endoplasmic reticulum membrane. Is active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
227 residues, UniProt reviewed canonical sequence.
>Q9NXI6|RNF186
1 MACTKTLQQS QPISAGATTT TTAVAPAGGH SGSTECDLEC LVCREPYSCP RLPKLLACQH
61 AFCAICLKLL LCVQDNTWSI TCPLCRKVTA VPGGLICSLR DHEAVVGQLA QPCTEVSLCP
121 QGLVDPADLA AGHPSLVGED GQDEVSANHV AARRLAAHLL LLALLIILIG PFIYPGVLRW
181 VLTFIIALAL LMSTLFCCLP STRGSCWPSS RTLFCREQKH SHISSIALocalizationUniProt · AlphaFold · HPA
Whether an antibody against RNF186 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 2
- Mean surface accessibility (rSASA)
- 0.53
- Highest tissue expression
- 123 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 123 nTPM
- epididymis: 64 nTPM
- small intestine: 42 nTPM
- pancreas: 42 nTPM
- kidney: 25 nTPM
- colon: 18 nTPM
Single-cell type
- epididymal principal cells: 331 nCPM
- enteric stem cells: 129 nCPM
- enteric transient amplifying cells: 91 nCPM
- colonocytes: 81 nCPM
- neuroendocrine cells: 64 nCPM
- paneth cells: 46 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
- cerebellum: 0.2 nTPM
- pons: 0.1 nTPM
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 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)
- 1.39
- gnomAD pLI
- 0.08
- gnomAD missense Z
- -0.16
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein autoubiquitination
- protein K29-linked ubiquitination
- protein K63-linked ubiquitination
- protein localization to mitochondrion
Molecular functions
- ubiquitin protein ligase activity
- ubiquitin protein ligase binding
- ubiquitin-protein transferase activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RNF186 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 RNF186 as an antibody target. Whether an autoantibody or antibody against RNF186 could matter depends on whether native RNF186 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RNF186 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 RNF186 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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