GO:0008053 | mitochondrial fusion |
Smith-Magenis syndrome chromosome region, candidate 7-like (human) |
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Synonym
AI452372, Smcr7l, A230016E22
Refseq ID | NM_178719 |
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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 |