12 genes in 10 celllines
General information | |
CEG ID: | CEGH0528 |
CEG_gene ID | Gene name(s) | Function | Condition | UniProt | Organism | Cellline |
---|---|---|---|---|---|---|
CEGH0528_DEG20102365 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | human |
CEGH0528_DEG20110716 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | human |
CEGH0528_DEG20121121 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | KBM7 |
CEGH0528_DEG20131193 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | HAP1 |
CEGH0528_DEG20141019 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | KBM7 |
CEGH0528_DEG20160909 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | Jiyoye |
CEGH0528_DEG20180671 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | A375 |
CEGH0528_DEG20191041 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | DLD1 |
CEGH0528_DEG20201255 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | GBM |
CEGH0528_DEG20211178 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | HCT116 |
CEGH0528_DEG20230933 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | HELA |
CEGH0528_DEG20241138 | OPA1 | optic atrophy 1 (autosomal dominant) | Rich medium | O60313 | Homo sapiens | REP1 |