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Gene Gene information from NCBI Gene database.
Entrez ID 93973
Gene name Actin related protein 8
Gene symbol ACTR8
Synonyms (NCBI Gene)
ARP8INO80NhArp8
Chromosome 3
Chromosome location 3p21.1
miRNA miRNA information provided by mirtarbase database.
184 Show/Hide all (184)
miRTarBase ID miRNA Experiments Reference
MIRT002578 hsa-miR-124-3p Microarray 15685193
MIRT002578 hsa-miR-124-3p Microarray;Other 15685193
MIRT029896 hsa-miR-26b-5p Microarray 19088304
MIRT441268 hsa-miR-218-5p HITS-CLIP 23212916
MIRT441268 hsa-miR-218-5p HITS-CLIP 23212916
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
38 Show/Hide all (38)
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000723 Process Telomere maintenance IEA
GO:0000723 Process Telomere maintenance ISO
GO:0005515 Function Protein binding IPI 16230350, 18163988, 18922472, 26496610, 33961781
GO:0005524 Function ATP binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619716 14672 ENSG00000113812
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H981
Protein name Actin-related protein 8 (hArp8) (INO80 complex subunit N)
Protein function Plays an important role in the functional organization of mitotic chromosomes. Exhibits low basal ATPase activity, and unable to polymerize.; Proposed core component of the chromatin remodeling INO80 complex which is involved in transc
PDB 4FO0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00022 Actin 43 → 621 Actin Family
Sequence
Sequence length 624
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
KEGG Pathway Reactome Pathway
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.).
5
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 Reference Evidence Score
Familial pancreatic carcinoma Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Hepatocellular carcinoma Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Lung cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Ovarian cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations