MUL1
Mitochondrial ubiquitin ligase activator of NFKB 1
Also known as: C1orf166, FLJ12875, GIDE, MAPL, MUL1_HUMAN, MULAN, RNF218
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q969V5
- Gene
- MUL1
- Ensembl
- ENSG00000090432
- Chromosome
- 1
- Canonical length
- 352 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Mitochondria,Cytosol
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
Enables several functions, including p53 binding activity; ubiquitin protein ligase binding activity; and ubiquitin-like protein transferase activity. Involved in several processes, including cellular response to exogenous dsRNA; negative regulation of defense response; and regulation of mitochondrion organization. Located in several cellular components, including mitochondrial outer membrane; neuronal cell body; and peroxisome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
352 residues, UniProt reviewed canonical sequence.
>Q969V5|MUL1
1 MESGGRPSLC QFILLGTTSV VTAALYSVYR QKARVSQELK GAKKVHLGED LKSILSEAPG
61 KCVPYAVIEG AVRSVKETLN SQFVENCKGV IQRLTLQEHK MVWNRTTHLW NDCSKIIHQR
121 TNTVPFDLVP HEDGVDVAVR VLKPLDSVDL GLETVYEKFH PSIQSFTDVI GHYISGERPK
181 GIQETEEMLK VGATLTGVGE LVLDNNSVRL QPPKQGMQYY LSSQDFDSLL QRQESSVRLW
241 KVLALVFGFA TCATLFFILR KQYLQRQERL RLKQMQEEFQ EHEAQLLSRA KPEDRESLKS
301 ACVVCLSSFK SCVFLECGHV CSCTECYRAL PEPKKCPICR QAITRVIPLY NSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MUL1 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)
- 0.34
- Highest tissue expression
- 47 nTPM
Expression across tissuesHPA
Tissue
- tongue: 47 nTPM
- parathyroid gland: 34 nTPM
- skeletal muscle: 34 nTPM
- heart muscle: 32 nTPM
- bone marrow: 27 nTPM
- choroid plexus: 27 nTPM
Single-cell type
- esophageal apical cells: 64 nCPM
- syncytiotrophoblasts: 45 nCPM
- cytotrophoblasts: 44 nCPM
- migrating cytotrophoblasts: 34 nCPM
- hofbauer cells: 31 nCPM
- epididymal clear cells: 31 nCPM
Immune cell
- eosinophil: 38 nTPM
- T-reg: 38 nTPM
- basophil: 36 nTPM
- intermediate monocyte: 35 nTPM
- MAIT T-cell: 35 nTPM
- total PBMC: 34 nTPM
Brain region
- choroid plexus: 29 nTPM
- medulla oblongata: 22 nTPM
- pons: 22 nTPM
- cerebellum: 21 nTPM
- white matter: 21 nTPM
- thalamus: 21 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)
- 1.15
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.86
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
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
- cellular response to exogenous dsRNA
- mitochondrial fission
- mitochondrion localization
- negative regulation of chemokine (C-C motif) ligand 5 production
- negative regulation of defense response to virus by host
- negative regulation of innate immune response
- negative regulation of mitochondrial fusion
- negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- negative regulation of type I interferon-mediated signaling pathway
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of dendrite extension
- positive regulation of mitochondrial fission
- positive regulation of protein sumoylation
- positive regulation of type 2 mitophagy
- protein destabilization
- protein polyubiquitination
- protein stabilization
- protein sumoylation
- protein ubiquitination
- regulation of mitochondrial membrane potential
- regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway
- regulation of mitochondrion organization
Molecular functions
- identical protein binding
- p53 binding
- SUMO transferase activity
- ubiquitin protein ligase activity
- ubiquitin protein ligase binding
- ubiquitin-protein transferase activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, RING-type
- Zinc finger, RING/FYVE/PHD-type
- MDM2/MDM4 and MUL1
- Zinc finger, C3HC4 type (RING finger)
- E3 Ubiquitin ligase MUL1-like
- E3 Ubiquitin ligase
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MUL1 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 MUL1 as an antibody target. Whether an autoantibody or antibody against MUL1 could matter depends on whether native MUL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MUL1 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 MUL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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