Gene Gene information from NCBI Gene database.
Entrez ID 125476
Gene name INO80 complex subunit C
Gene symbol INO80C
Synonyms (NCBI Gene)
C18orf37IES6hIes6
Chromosome 18
Chromosome location 18q12.2
miRNA miRNA information provided by mirtarbase database.
93
miRTarBase ID miRNA Experiments Reference
MIRT002689 hsa-miR-124-3p Proteomics;Microarray 18668037
MIRT002689 hsa-miR-124-3p Microarray 15685193
MIRT657182 hsa-miR-494-3p HITS-CLIP 23824327
MIRT657181 hsa-miR-6509-3p HITS-CLIP 23824327
MIRT657180 hsa-miR-4436b-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
GO ID Ontology Definition Evidence Reference
GO:0000723 Process Telomere maintenance IEA
GO:0000723 Process Telomere maintenance ISO
GO:0001650 Component Fibrillar center IDA
GO:0005515 Function Protein binding IPI 26496610, 32814053, 33961781, 35271311
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6PI98
Protein name INO80 complex subunit C (IES6 homolog) (hIes6)
Protein function Proposed core component of the chromatin remodeling INO80 complex which is involved in transcriptional regulation, DNA replication and probably DNA repair.
PDB 7ZI4
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08265 YL1_C 142 170 YL1 nuclear protein C-terminal domain Domain
Sequence
MAAQIPIVATTSTPGIVRNSKKRPASPSHNGSSGGGYGASKKKKASASSFAQGISMEAMS
ENKMVPSEFSTGPVEKAAKPLPFKDPNFVHSGHGGAVAGKKNRTWKNLKQILASERALPW
QLNDPNYFSIDAPPSFKPAKKYSDVSGLLANYTDPQSKLRFSTIEEFSYIRRLPSDVVTG
YLALRKATSIVP
Sequence length 192
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  ATP-dependent chromatin remodeling   UCH proteinases
DNA Damage Recognition in GG-NER
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EOSINOPHILIC ESOPHAGITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Anxiety Anxiety Disorder BEFREE 31391069
★☆☆☆☆
Found in Text Mining only
Anxiety Disorders Anxiety Disorder BEFREE 31391069
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 28954733 Associate
★☆☆☆☆
Found in Text Mining only
Depressive disorder Mental Depression BEFREE 31391069
★☆☆☆☆
Found in Text Mining only
Leukemia Myeloid Acute Myeloid leukemia Pubtator 31537905 Associate
★☆☆☆☆
Found in Text Mining only
Leukemia, Myelocytic, Acute Leukemia BEFREE 31537905
★☆☆☆☆
Found in Text Mining only
Mental Depression Mental Depression BEFREE 31391069
★☆☆☆☆
Found in Text Mining only
Post-Traumatic Stress Disorder Stress Disorder BEFREE 31391069
★☆☆☆☆
Found in Text Mining only
Respiratory Distress Syndrome, Adult Respiratory Distress Syndrome BEFREE 31391069
★☆☆☆☆
Found in Text Mining only