| Disease ID | Disease name | Source of annotation with ITGA7 | OMIM link | Number of associated genes | genes |
|---|---|---|---|---|---|
| 613204 | MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY | ClinVar, OMIM | link to OMIM | 1 | ITGA7 |
Download the gene annotation in CSV format
| KEGG pathway | KEGG ID | KEGG IC |
|---|---|---|
| ECM-receptor interaction | hsa04512 | 6.09 |
| Focal adhesion | hsa04510 | 4.92 |
| Hypertrophic cardiomyopathy (HCM) | hsa05410 | 6.21 |
| Arrhythmogenic right ventricular cardiomyopathy (ARVC) | hsa05412 | 6.32 |
| PI3K-Akt signaling pathway | hsa04151 | 4.21 |
| Dilated cardiomyopathy | hsa05414 | 6.08 |
| Regulation of actin cytoskeleton | hsa04810 | 4.9 |
| REACTOME pathway | REACTOME ID | REACTOME IC |
|---|---|---|
| ECM proteoglycans | R-HSA-3000178 | 6.75 |
| Integrin cell surface interactions | R-HSA-216083 | 6.57 |
| Extracellular matrix organization | R-HSA-1474244 | 4.91 |
| Laminin interactions | R-HSA-3000157 | 8.08 |
| GO term | GO ID | GO IC |
|---|---|---|
| cation binding | GO:0043169 | 1.4 |
| metal ion binding | GO:0046872 | 1.41 |
| binding | GO:0005488 | 0.18 |
| protein binding | GO:0005515 | 0.46 |
| ion binding | GO:0043167 | 1.36 |