| Gene Symbol |
C12orf65
|
| Entrez Gene |
91574
|
| Alt Symbol |
COXPD7, SPG55
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
chromosome 12 open reading frame 65
|
| Other Description |
probable peptide chain release factor C12orf65, mitochondrial
|
| Swissprots |
Q8WUC6 Q9H3J6
|
| Accessions |
EAW98395 EAW98396 Q9H3J6 AF061733 AAG43144 AK025908 AK095982 BAC04665 AK126043 BC018145 AAH18145 BC020885 AAH20885 BC062329 AAH62329 BI850864 BU507560 HQ448204 ADQ32685 XM_005253630 XP_005253687 XM_011538980 XP_011537282 XM_011538981 XP_011537283 XM_011538982 XP_011537284 NM_001143905 NP_001137377 NM_001194995 NP_001181924 NM_152269 NP_689482
|
| Function |
May act as a codon-independent translation release factor that has lost all stop codon specificity and directs the termination of translation in mitochondrion. May help rescuing stalled mitoribosomes during translation (By similarity). {ECO:0000250}.
|
| Subcellular Location |
Mitochondrion {ECO:0000269|PubMed:20186120}.
|