INO80C
INO80 complex subunit C
Also known as: C18orf37, FLJ38183, hIes6, IES6, IN80C_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6PI98
- Gene
- INO80C
- Ensembl
- ENSG00000153391
- Chromosome
- 18
- Canonical length
- 192 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Nucleoli fibrillar center,Cytosol
OverviewNCBI Gene
Involved in several processes, including chromatin remodeling; regulation of chromosome organization; and regulation of nucleobase-containing compound metabolic process. Located in cytosol; fibrillar center; and nucleoplasm. Part of Ino80 complex and MLL1 complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
192 residues, UniProt reviewed canonical sequence.
>Q6PI98|INO80C
1 MAAQIPIVAT TSTPGIVRNS KKRPASPSHN GSSGGGYGAS KKKKASASSF AQGISMEAMS
61 ENKMVPSEFS TGPVEKAAKP LPFKDPNFVH SGHGGAVAGK KNRTWKNLKQ ILASERALPW
121 QLNDPNYFSI DAPPSFKPAK KYSDVSGLLA NYTDPQSKLR FSTIEEFSYI RRLPSDVVTG
181 YLALRKATSI VPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against INO80C 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)
- 0.61
- Highest tissue expression
- 86 nTPM
Expression across tissuesHPA
Tissue
- testis: 86 nTPM
- esophagus: 45 nTPM
- bone marrow: 44 nTPM
- skeletal muscle: 40 nTPM
- choroid plexus: 39 nTPM
- skin: 38 nTPM
Single-cell type
- late primary spermatocytes: 89 nCPM
- early spermatids: 32 nCPM
- gastric chief cells: 28 nCPM
- esophageal apical cells: 20 nCPM
- suprabasal keratinocytes: 14 nCPM
- late spermatids: 13 nCPM
Immune cell
- eosinophil: 36 nTPM
- plasmacytoid DC: 34 nTPM
- memory B-cell: 25 nTPM
- neutrophil: 23 nTPM
- myeloid DC: 22 nTPM
- T-reg: 22 nTPM
Brain region
- hypothalamus: 50 nTPM
- choroid plexus: 49 nTPM
- cerebellum: 35 nTPM
- pons: 35 nTPM
- basal ganglia: 35 nTPM
- cerebral cortex: 33 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)
- 1.42
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.1
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chromatin remodeling
- DNA recombination
- DNA repair
- positive regulation of DNA repair
- positive regulation of DNA-templated transcription
- positive regulation of telomere maintenance in response to DNA damage
- regulation of cell cycle
- regulation of chromosome organization
- regulation of DNA repair
- regulation of DNA replication
- regulation of DNA strand elongation
- regulation of embryonic development
- telomere maintenance
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Vps72/YL1, C-terminal
- YL1 nuclear protein C-terminal domain
- INO80 complex, subunit Ies6
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of INO80C 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 INO80C as an antibody target. Whether an autoantibody or antibody against INO80C could matter depends on whether native INO80C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
INO80C 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 INO80C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...