| Gene Symbol |
OPA3
|
| Entrez Gene |
80207
|
| Alt Symbol |
MGA3
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
|
| Other Description |
Optic atrophy 3 (Iraqi-Jewish 'optic atrophy plus')|optic atrophy 3 protein
|
| Swissprots |
Q8N784 Q9H6K4 Q6P384
|
| Accessions |
CAK32367 EAW57367 Q9H6K4 AK025840 BAB15255 AK098798 BAC05415 AK296429 BAG59089 AM392686 CAL37564 BC005059 AAH05059 BC047316 AAH47316 BC064146 AAH64146 BU617706 CA944687 DB034102 EU832556 ACE86958 XM_005259278 XP_005259335 XM_006723403 XP_006723466 XM_011527348 XP_011525650 NM_001017989 NP_001017989 NM_025136 NP_079412
|
| Function |
May play some role in mitochondrial processes.
|
| Subcellular Location |
Mitochondrion {ECO:0000305}.
|
| Tissue Specificity |
Ubiquitous. Most prominent expression in skeletal muscle and kidney. {ECO:0000269|PubMed:11668429}.
|
