Disease ID | Disease name | Source of annotation with NDUFB11 | OMIM link | Number of associated genes | genes |
---|---|---|---|---|---|
PS309801 | LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES | ClinVar, OMIM | link to OMIM | 3 | COX7B, NDUFB11, HCCS |
Download the gene annotation in CSV format
KEGG pathway | KEGG ID | KEGG IC |
---|---|---|
Oxidative phosphorylation | hsa00190 | 5.69 |
Metabolic pathways | hsa01100 | 2.49 |
Non-alcoholic fatty liver disease (NAFLD) | hsa04932 | 5.51 |
Huntington's disease | hsa05016 | 5.17 |
Alzheimer's disease | hsa05010 | 5.34 |
Parkinson's disease | hsa05012 | 5.59 |
REACTOME pathway | REACTOME ID | REACTOME IC |
---|---|---|
Metabolism | R-HSA-1430728 | 2.34 |
Respiratory electron transport | R-HSA-611105 | 6.44 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | R-HSA-163200 | 6.12 |
The citric acid (TCA) cycle and respiratory electron transport | R-HSA-1428517 | 5.71 |
GO term | GO ID | GO IC |
---|---|---|
binding | GO:0005488 | 0.18 |
protein binding | GO:0005515 | 0.46 |