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INO80 INO80 complex ATPase subunit [ Homo sapiens (human) ]

Gene ID: 54617, updated on 25-Nov-2021

Summary

Official Symbol
INO80provided by HGNC
Official Full Name
INO80 complex ATPase subunitprovided by HGNC
Primary source
HGNC:HGNC:26956
See related
Ensembl:ENSG00000128908 MIM:610169
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
INOC1; INO80A
Summary
This gene encodes a subunit of the chromatin remodeling complex, which is classified into subfamilies depending on sequence features apart from the conserved ATPase domain. This protein is the catalytic ATPase subunit of the INO80 chromatin remodeling complex, which is characterized by a DNA-binding domain. This protein is proposed to bind DNA and be recruited by the YY1 transcription factor to activate certain genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
Expression
Ubiquitous expression in bone marrow (RPKM 5.6), testis (RPKM 5.5) and 25 other tissues See more
Orthologs
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Genomic context

See INO80 in Genome Data Viewer
Location:
15q15.1
Exon count:
37
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (40978880..41117778, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (41271078..41408478, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370789 Neighboring gene iron-sulfur cluster assembly 1 pseudogene 4 Neighboring gene ChaC glutathione specific gamma-glutamylcyclotransferase 1 Neighboring gene uncharacterized LOC112268144 Neighboring gene uncharacterized LOC105376713 Neighboring gene INO80 antisense RNA 1 Neighboring gene CYCS pseudogene 2 Neighboring gene CIBAR1 pseudogene 1 Neighboring gene RNA, 7SL, cytoplasmic 497, pseudogene Neighboring gene exonuclease 3'-5' domain containing 1

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Homology

Clone Names

  • KIAA1259

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables ATP binding IEA
Inferred from Electronic Annotation
more info
 
enables ATP hydrolysis activity IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
enables ATP-dependent activity, acting on DNA IDA
Inferred from Direct Assay
more info
PubMed 
enables DNA binding IDA
Inferred from Direct Assay
more info
PubMed 
enables actin binding IEA
Inferred from Electronic Annotation
more info
 
enables alpha-tubulin binding IMP
Inferred from Mutant Phenotype
more info
PubMed 
enables histone binding IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Process Evidence Code Pubs
involved_in DNA repair IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
involved_in UV-damage excision repair IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in cell division IEA
Inferred from Electronic Annotation
more info
 
involved_in cellular response to UV IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in cellular response to ionizing radiation IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in chromatin remodeling IDA
Inferred from Direct Assay
more info
PubMed 
involved_in chromatin remodeling ISS
Inferred from Sequence or Structural Similarity
more info
 
involved_in double-strand break repair IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in double-strand break repair via homologous recombination IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in mitotic sister chromatid segregation IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in nucleosome mobilization IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
involved_in nucleosome mobilization IDA
Inferred from Direct Assay
more info
PubMed 
involved_in positive regulation of cell growth IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in positive regulation of nuclear cell cycle DNA replication IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in positive regulation of transcription by RNA polymerase II IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in positive regulation of transcription, DNA-templated IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in regulation of DNA replication IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in regulation of DNA strand elongation IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in regulation of G1/S transition of mitotic cell cycle IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in regulation of cell cycle IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in regulation of chromosome organization IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in regulation of transcription from RNA polymerase II promoter in response to stress IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
involved_in spindle assembly IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in transcription, DNA-templated IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
part_of Ino80 complex IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
part_of Ino80 complex IDA
Inferred from Direct Assay
more info
PubMed 
located_in cytosol IDA
Inferred from Direct Assay
more info
 
located_in microtubule IEA
Inferred from Electronic Annotation
more info
 
located_in nuclear body IDA
Inferred from Direct Assay
more info
 
located_in nucleoplasm IDA
Inferred from Direct Assay
more info
 
located_in nucleoplasm TAS
Traceable Author Statement
more info
 
located_in nucleus IDA
Inferred from Direct Assay
more info
PubMed 
located_in spindle IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
chromatin-remodeling ATPase INO80
Names
DNA helicase INO80
DNA helicase-related INO80 complex homolog 1
DNA helicase-related protein INO80
INO80 complex subunit A
homolog of yeast INO80
putative DNA helicase INO80 complex homolog 1
NP_060023.1
XP_011519987.1
XP_011519988.1

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_017163.2 RefSeqGene

    Range
    6499..143899
    Download
    GenBank, FASTA, Sequence Viewer (Graphics), LRG_1233

mRNA and Protein(s)

  1. NM_017553.3NP_060023.1  chromatin-remodeling ATPase INO80

    See identical proteins and their annotated locations for NP_060023.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) represents the longer transcript and encodes the functional protein.
    Source sequence(s)
    AB033085, AC020661, AL137280, BC046115, CB155560, DB458576
    Consensus CDS
    CCDS10071.1
    UniProtKB/Swiss-Prot
    Q9ULG1
    UniProtKB/TrEMBL
    A0A024R9R7
    Related
    ENSP00000497609.1, ENST00000648947.1
    Conserved Domains (3) summary
    pfam00176
    Location:521822
    SNF2_N; SNF2 family N-terminal domain
    pfam13892
    Location:273402
    DBINO; DNA-binding domain
    cl26465
    Location:10941252
    SNF2_N; SNF2 family N-terminal domain

RNA

  1. NR_104038.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks an alternate internal exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AC020661, AC021753
    Related
    ENST00000558357.6

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    40978880..41117778 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_011521686.3XP_011519988.1  chromatin-remodeling ATPase INO80 isoform X2

    Conserved Domains (3) summary
    PLN03142
    Location:16181
    PLN03142; Probable chromatin-remodeling complex ATPase chain; Provisional
    cd18793
    Location:440575
    SF2_C_SNF; C-terminal helicase domain of the SNF family helicases
    cl28899
    Location:996
    DEAD-like_helicase_N; N-terminal helicase domain of the DEAD-box helicase superfamily
  2. XM_011521685.3XP_011519987.1  chromatin-remodeling ATPase INO80 isoform X1

    Conserved Domains (4) summary
    COG0553
    Location:348866
    HepA; Superfamily II DNA or RNA helicase, SNF2 family [Transcription, Replication, recombination and repair]
    cd18793
    Location:10901171
    SF2_C_SNF; C-terminal helicase domain of the SNF family helicases
    cd18002
    Location:518746
    DEXQc_INO80; DEAQ-box helicase domain of INO80
    pfam13892
    Location:273402
    DBINO; DNA-binding domain

RNA

  1. XR_001751322.2 RNA Sequence

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_032196.3: Suppressed sequence

    Description
    NM_032196.3: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
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