| GO:0008053 | mitochondrial fusion |
Smith-Magenis syndrome chromosome region, candidate 7-like (human) |
詳細情報を見る |
同義遺伝子名
AI452372, Smcr7l, A230016E22
| Refseq ID | NM_178719 |
|---|---|
| Gene ID | 239555 |
| Unigene ID | Mm.307163 |
| Probe set ID | - |
| Ensembl ID | ENSMUSG00000022412 |
| - |
Biological Process
Cellular Component
| GO:0016021 | integral to membrane |
| GO:0016020 | membrane |
| GO:0005741 | mitochondrial outer membrane |
| GO:0005739 | mitochondrion |





