INO80D (INO80 complex subunit D)

2011-06-01  

Identity

HGNC
LOCATION
2q33.3
LOCUSID
ALIAS
-
FUSION GENES

Other Information

Locus ID:

NCBI: 54891
HGNC: 25997
Ensembl: ENSG00000114933

Variants:

dbSNP: 54891
ClinVar: 54891
TCGA: ENSG00000114933
COSMIC: INO80D

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000114933ENST00000403263Q53TQ3
ENSG00000114933ENST00000414320C9JLV2
ENSG00000114933ENST00000424117C9JLZ4

Expression (GTEx)

0
5
10
15

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

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
251220532014Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness.7
297504212018Genome-wide analysis of lncRNAs in 3'-untranslated regions: CR933609 acts as a decoy to protect the INO80D gene.1

Citation

Dessen P

INO80D (INO80 complex subunit D)

Atlas Genet Cytogenet Oncol Haematol. 2011-06-01

Online version: http://atlasgeneticsoncology.org/gene/52248/ino80d