ARMC8
Armadillo repeat-containing protein 8
Also known as: ARMC8_HUMAN, DKFZP434A043, GID5, HSPC056, VID28
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IUR7
- Gene
- ARMC8
- Ensembl
- ENSG00000114098
- Chromosome
- 3
- Canonical length
- 673 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Cytosol
OverviewNCBI Gene
Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Located in cytosol and nucleoplasm. Part of ubiquitin ligase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
673 residues, UniProt reviewed canonical sequence.
>Q8IUR7|ARMC8
1 MACLLETPIR MSVLSEVTAS SRHYVDRLFD PDPQKVLQGV IDMKNAVIGN NKQKANLIVL
61 GAVPRLLYLL QQETSSTELK TECAVVLGSL AMGTENNVKS LLDCHIIPAL LQGLLSPDLK
121 FIEACLRCLR TIFTSPVTPE ELLYTDATVI PHLMALLSRS RYTQEYICQI FSHCCKGPDH
181 QTILFNHGAV QNIAHLLTSL SYKVRMQALK CFSVLAFENP QVSMTLVNVL VDGELLPQIF
241 VKMLQRDKPI EMQLTSAKCL TYMCRAGAIR TDDNCIVLKT LPCLVRMCSK ERLLEERVEG
301 AETLAYLIEP DVELQRIASI TDHLIAMLAD YFKYPSSVSA ITDIKRLDHD LKHAHELRQA
361 AFKLYASLGA NDEDIRKKII ETENMMDRIV TGLSESSVKV RLAAVRCLHS LSRSVQQLRT
421 SFQDHAVWKP LMKVLQNAPD EILVVASSML CNLLLEFSPS KEPILESGAV ELLCGLTQSE
481 NPALRVNGIW ALMNMAFQAE QKIKADILRS LSTEQLFRLL SDSDLNVLMK TLGLLRNLLS
541 TRPHIDKIMS THGKQIMQAV TLILEGEHNI EVKEQTLCIL ANIADGTTAK DLIMTNDDIL
601 QKIKYYMGHS HVKLQLAAMF CISNLIWNEE EGSQERQDKL RDMGIVDILH KLSQSPDSNL
661 CDKAKMALQQ YLALocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARMC8 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)
- 0.24
- Highest tissue expression
- 57 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 57 nTPM
- skeletal muscle: 37 nTPM
- cerebellum: 36 nTPM
- tongue: 32 nTPM
- retina: 24 nTPM
- blood vessel: 24 nTPM
Single-cell type
- neutrophil progenitors: 322 nCPM
- myonuclei: 257 nCPM
- neutrophils: 256 nCPM
- choroid plexus epithelial cells: 224 nCPM
- megakaryocyte-erythroid progenitors: 204 nCPM
- oligodendrocyte progenitor cells: 198 nCPM
Immune cell
- basophil: 80 nTPM
- eosinophil: 75 nTPM
- T-reg: 51 nTPM
- memory B-cell: 49 nTPM
- NK-cell: 49 nTPM
- non-classical monocyte: 46 nTPM
Brain region
- cerebellum: 97 nTPM
- choroid plexus: 65 nTPM
- white matter: 49 nTPM
- pons: 48 nTPM
- hypothalamus: 46 nTPM
- basal ganglia: 45 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)
- 0.17
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.88
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 13% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Armadillo
- Armadillo-like helical
- Armadillo-type fold
- Armadillo/beta-catenin-like repeat
- Armadillo-type fold containing protein ARMC8/Vid28
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARMC8 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 ARMC8 as an antibody target. Whether an autoantibody or antibody against ARMC8 could matter depends on whether native ARMC8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARMC8 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 ARMC8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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