| 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}. |
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) , ELISA Kit - MBS9317976 from MyBioSource
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Optic Atrophy 3 (OPA3), ELISA Kit - MBS9312262 from MyBioSource
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Human OPA3 ELISA Kit - E027735 from Biobool
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anti-OPA3 antibody - ARG56390 from Arigo Biolaboratories
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