GENE：COX7B2
GeneInfo:
| GeneAttribute | GeneDescription |
|---|---|
| GeneSymbol | COX7B2 |
| FullNmae | cytochrome c oxidase subunit 7B2 |
| LocusType | gene with protein product |
| Status | Approved |
| HGNC_id | HGNC:24381 |
| EnsembleID | ENSG00000170516 |
| Uniprot | Q8TF08 |
Protein Structure:
Gene Description in Publicaton:
| GeneSymbol | CellDeathType | PMID | Description | GeneType |
|---|---|---|---|---|
| COX7B2 | immunogenic | 38538696 | The 18 RCD signatures collected from previous studies. Supplementary Table of Figures.xlsx (https://github.com/zwxiangya/RCDscore) | retulator signature |
Go Annotation:
| GeneSymbol | Go id |
|---|---|
| COX7B2 | GO:0005739,GO:0005746,GO:0006123,GO:0007283,GO:0045277 |
KEGG Annotation:
| GeneSymbol | GeneID | Pathway | Pathway Name |
|---|---|---|---|
| COX7B2 | hsa:170712 | path:hsa00190 | Oxidative phosphorylation - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa01100 | Metabolic pathways - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa04260 | Cardiac muscle contraction - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa04714 | Thermogenesis - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa04932 | Non-alcoholic fatty liver disease - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa05010 | Alzheimer disease - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa05012 | Parkinson disease - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa05014 | Amyotrophic lateral sclerosis - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa05016 | Huntington disease - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa05020 | Prion disease - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa05022 | Pathways of neurodegeneration - multiple diseases - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa05208 | Chemical carcinogenesis - reactive oxygen species - Homo sapiens (human) |
| COX7B2 | hsa:170712 | path:hsa05415 | Diabetic cardiomyopathy - Homo sapiens (human) |