ARK2C
E3 ubiquitin-protein ligase ARK2C
Also known as: ARK2C_HUMAN, ARKL2, lncAMPC, RNF111L2, RNF165
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZSG1
- Gene
- ARK2C
- Ensembl
- ENSG00000141622
- Chromosome
- 18
- Canonical length
- 346 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in motor neuron axon guidance and positive regulation of BMP signaling pathway. Predicted to act upstream of or within several processes, including forelimb morphogenesis; nervous system development; and protein polyubiquitination. Predicted to be part of protein-containing complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
346 residues, UniProt reviewed canonical sequence.
>Q6ZSG1|ARK2C
1 MVLVHVGYLV LPVFGSVRNR GAPFQRSQHP HATSCRHFHL GPPQPQQLAP DFPLAHPVQS
61 QPGLSAHMAP AHQHSGALHQ SLTPLPTLQF QDVTGPSFLP QALHQQYLLQ QQLLEAQHRR
121 LVSHPRRSQE RVSVHPHRLH PSFDFGQLQT PQPRYLAEGT DWDLSVDAGL SPAQFQVRPI
181 PQHYQHYLAT PRMHHFPRNS SSTQMVVHEI RNYPYPQLHF LALQGLNPSR HTSAVRESYE
241 ELLQLEDRLG NVTRGAVQNT IERFTFPHKY KKRRPQDGKG KKDEGEESDT DEKCTICLSM
301 LEDGEDVRRL PCMHLFHQLC VDQWLAMSKK CPICRVDIET QLGADSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARK2C 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)
- 0.6
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 22 nTPM
- retina: 17 nTPM
- cerebral cortex: 5.1 nTPM
- liver: 4.7 nTPM
- pituitary gland: 3.7 nTPM
- thyroid gland: 3.7 nTPM
Single-cell type
- retinal amacrine cells: 178 nCPM
- retinal horizontal cells: 122 nCPM
- cone photoreceptor cells: 93 nCPM
- lactotrophs: 84 nCPM
- brain excitatory neurons: 79 nCPM
- ependymal cells: 76 nCPM
Immune cell
- NK-cell: 1.1 nTPM
- plasmacytoid DC: 0.4 nTPM
- MAIT T-cell: 0.3 nTPM
- eosinophil: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
Brain region
- cerebellum: 32 nTPM
- cerebral cortex: 29 nTPM
- hippocampal formation: 26 nTPM
- amygdala: 22 nTPM
- basal ganglia: 21 nTPM
- white matter: 19 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)
- 0.32
- gnomAD pLI
- 0.97
- DepMap mean gene effect
- 0.06
- 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
- forelimb morphogenesis
- innervation
- motor neuron axon guidance
- muscle structure development
- positive regulation of BMP signaling pathway
- protein catabolic process
- protein polyubiquitination
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, RING-type
- Zinc finger, RING-CH-type
- Zinc finger, RING/FYVE/PHD-type
- Ring finger domain
- E3 ubiquitin-protein ligase MBR1/2-like
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ARK2C as an antibody target. Whether an autoantibody or antibody against ARK2C could matter depends on whether native ARK2C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARK2C 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 ARK2C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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