MARCHF8
E3 ubiquitin-protein ligase MARCHF8
Also known as: c-MIR, CMIR, MARCH-VIII, MARCH8, MARH8_HUMAN, MIR, RNF178
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5T0T0
- Gene
- MARCHF8
- Ensembl
- ENSG00000165406
- Chromosome
- 10
- Canonical length
- 291 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
MARCH8 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH8 induces the internalization of several membrane glycoproteins (Goto et al., 2003 [PubMed 12582153]; Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010]
Canonical amino-acid sequenceUniProt
291 residues, UniProt reviewed canonical sequence.
>Q5T0T0|MARCHF8
1 MSMPLHQISA IPSQDAISAR VYRSKTKEKE REEQNEKTLG HFMSHSSNIS KAGSPPSASA
61 PAPVSSFSRT SITPSSQDIC RICHCEGDDE SPLITPCHCT GSLHFVHQAC LQQWIKSSDT
121 RCCELCKYEF IMETKLKPLR KWEKLQMTSS ERRKIMCSVT FHVIAITCVV WSLYVLIDRT
181 AEEIKQGQAT GILEWPFWTK LVVVAIGFTG GLLFMYVQCK VYVQLWKRLK AYNRVIYVQN
241 CPETSKKNIF EKSPLTEPNF ENKHGYGICH SDTNSSCCTE PEDTGAEIIH VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MARCHF8 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)
- 0.51
- Highest tissue expression
- 53 nTPM
Expression across tissuesHPA
Tissue
- testis: 53 nTPM
- bone marrow: 46 nTPM
- pancreas: 25 nTPM
- cerebellum: 21 nTPM
- small intestine: 21 nTPM
- colon: 20 nTPM
Single-cell type
- early spermatids: 393 nCPM
- cone photoreceptor cells: 292 nCPM
- late spermatids: 165 nCPM
- b-cells: 123 nCPM
- choroid plexus epithelial cells: 112 nCPM
- oligodendrocytes: 108 nCPM
Immune cell
- neutrophil: 14 nTPM
- basophil: 14 nTPM
- eosinophil: 11 nTPM
- NK-cell: 8.5 nTPM
- naive B-cell: 5.4 nTPM
- MAIT T-cell: 4.5 nTPM
Brain region
- white matter: 72 nTPM
- medulla oblongata: 59 nTPM
- cerebellum: 58 nTPM
- basal ganglia: 56 nTPM
- pons: 53 nTPM
- thalamus: 52 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)
- 1.31
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.08
- 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
- adaptive immune response
- antigen processing and presentation of peptide antigen via MHC class II
- immune response
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein polyubiquitination
Molecular functions
- MHC protein binding
- ubiquitin protein ligase activity
- ubiquitin-protein transferase activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MARCHF8 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 MARCHF8 as an antibody target. Whether an autoantibody or antibody against MARCHF8 could matter depends on whether native MARCHF8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MARCHF8 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 MARCHF8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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