Gene Gene information from NCBI Gene database.
Entrez ID 54891
Gene name INO80 complex subunit D
Gene symbol INO80D
Synonyms (NCBI Gene)
-
Chromosome 2
Chromosome location 2q33.3
miRNA miRNA information provided by mirtarbase database.
1524
miRTarBase ID miRNA Experiments Reference
MIRT027306 hsa-miR-101-3p Sequencing 20371350
MIRT028742 hsa-miR-27a-3p Sequencing 20371350
MIRT051164 hsa-miR-16-5p CLASH 23622248
MIRT045886 hsa-miR-128-3p CLASH 23622248
MIRT044540 hsa-miR-320a CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
23
GO ID Ontology Definition Evidence Reference
GO:0000723 Process Telomere maintenance IEA
GO:0000723 Process Telomere maintenance ISO
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619207 25997 ENSG00000114933
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q53TQ3
Protein name INO80 complex subunit D
Protein function Putative regulatory component of the chromatin remodeling INO80 complex which is involved in transcriptional regulation, DNA replication and probably DNA repair.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13891 zf-C3Hc3H 18 79 Potential DNA-binding domain Domain
PF13891 zf-C3Hc3H 447 511 Potential DNA-binding domain Domain
Sequence
MYEGKHIHFSEVDNKPLCSYSPKLCKQRRLNGYAFCIRHVLEDKTAPFKQCEYVAKYNSQ
RCTNPIPKSEDRRYCNSHL
QVLGFIPKKERKKKNDPIDEVKVRHQMDTMAFSLTVPTLAL
KMPNGLDGMSLSPPGARVPLHYLETELEDPFAFNEEDDDLKKGATVRKKLQSKLAQNRQR
QRETEILKVRQEHFSPPPAPSQQQPPQQHSHLSPLSTSLKPPAPPQGSVCKSPQPQNTSL
PMQGVAPTTHTIAQARQLSHKRPLPLLPSSRAPTVDPPRTDRILMKATAFSPHFSCISRL
QRLVKLCTQKHQLDTDLFPHLGLDWSEESGEEPEDSEQASPYQVAWSIRETLRYQRHASD
DDDAESRSSRVTQLCTYFQQKYKHLCRLERAESRQKKCRHTFRKALLQAASKEPECTGQL
IQELRRAACSRTSISRTKLREVEPAACSGTVKGEQCANKALPFTRHCFQHILLNHSQQLF
SSCTAKFADGQQCSVPVFDITHQTPLCEEHA
KKMDNFLRGDNSRKVQHQQQRKPRKKTKP
PALTKKHKKKRRRGPRRPQKPIPPAVPQGNLSMPASVSLPVEASHIRSPSTPELSADELP
DDIANEITDIPHDLELNQEDFSDVLPRLPDDLQDFDFFEGKNGDLLPTTEEAEELERALQ
AVTSLECLSTIGVLAQSDGVPVQELSDRGIGVFSTGTGASGIQSLSREVNTDLGELLNGR
IVHDNFSSLELDENLLRSATLSNPPTPLAGQIQGQFSAPANVGLTSATLISQSALGERAF
PGQFHGLHDGSHASQRPHPAQLLSKADDLITSRQQYSSDHSHSSPHGSHYDSEHVPSPYS
DHITSPHTTSYSGDNMAATFSAEMPIMAQHLLPTQLEVPLGGVVNPRTHWGNLPVNLGDP
SPFSNLLGADGHLLSTSLSTPPTTSNSETTQPAFATVTPSSSSVLPGLPQTSFSGMGPSA
ELMASTSPKQQLPQFSAAFGHQLSSHSGIPKDLQPSHSSIAPPTGFTVTGATATSTNNAS
SPFPSPN
Sequence length 1027
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 categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Malignant tumor of esophagus Uncertain significance rs770510485 RCV005932202
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Stimulate 30670769
Carcinoma Renal Cell Associate 24899691
Polycystic Ovary Syndrome Associate 39585802