Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 54891
HGNC: 25997
Ensembl: ENSG00000114933
Variants:
dbSNP: 54891
ClinVar: 54891
TCGA: ENSG00000114933
COSMIC: INO80D
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000114933 | ENST00000403263 | Q53TQ3 |
| ENSG00000114933 | ENST00000414320 | C9JLV2 |
| ENSG00000114933 | ENST00000424117 | C9JLZ4 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 29750421 | 2018 | Genome-wide analysis of lncRNAs in 3'-untranslated regions: CR933609 acts as a decoy to protect the INO80D gene. | 6 |
| 29750421 | 2018 | Genome-wide analysis of lncRNAs in 3'-untranslated regions: CR933609 acts as a decoy to protect the INO80D gene. | 6 |
| 25122053 | 2014 | Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness. | 10 |
| 25122053 | 2014 | Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness. | 10 |
Citation
Dessen P
INO80D (INO80 complex subunit D)
Atlas Genet Cytogenet Oncol Haematol. 2011-06-01
Online version: http://atlasgeneticsoncology.org/gene/52248/ino80d
