INO80B (INO80 complex subunit B)

2007-04-01  

Identity

HGNC
LOCATION
2p13.1
LOCUSID
ALIAS
HMGA1L4,HMGIYL4,IES2,PAP-1BP,PAPA-1,PAPA1,ZNHIT4,hIes2
FUSION GENES

Other Information

Locus ID:

NCBI: 83444
MIM: 616456
HGNC: 13324
Ensembl: ENSG00000115274

Variants:

dbSNP: 83444
ClinVar: 83444
TCGA: ENSG00000115274
COSMIC: INO80B

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000115274ENST00000233331Q9C086
ENSG00000115274ENST00000409493B8ZZH7
ENSG00000115274ENST00000409917B8ZZ93
ENSG00000115274ENST00000431187C9JKY0
ENSG00000115274ENST00000455562H7C171

Expression (GTEx)

0
50
100
150

Pathways

PathwaySourceExternal ID
Metabolism of proteinsREACTOMER-HSA-392499
Post-translational protein modificationREACTOMER-HSA-597592
DNA RepairREACTOMER-HSA-73894
Nucleotide Excision RepairREACTOMER-HSA-5696398
Global Genome Nucleotide Excision Repair (GG-NER)REACTOMER-HSA-5696399
DNA Damage Recognition in GG-NERREACTOMER-HSA-5696394
DeubiquitinationREACTOMER-HSA-5688426
UCH proteinasesREACTOMER-HSA-5689603

References

Pubmed IDYearTitleCitations
251433932015Susceptibility allele-specific loss of miR-1324-mediated silencing of the INO80B chromatin-assembly complex gene in pre-eclampsia.1

Citation

Dessen P

INO80B (INO80 complex subunit B)

Atlas Genet Cytogenet Oncol Haematol. 2007-04-01

Online version: http://atlasgeneticsoncology.org/gene/47220/ino80b