| Type | Description |
|---|---|
| Definition | optic atrophy 3 |
| Date | Results | Publications |
|---|---|---|
| 2017-07-15 12:41:00 | Opa3(L122P) mice displayed craniofacial abnormalities, including undergrowth of the lower mandible, accompanied in some individuals by cranial asymmetry and incisor malocclusion | 27106103 |
| 2013-03-30 11:29:00 | Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome. | 22869679 |
| 2011-09-03 10:41:00 | Mutant Opa3 protein retains its mitochondrial localization and induces disrupted mitochondrial morphology. Opa3 accumulates in the lens. The results may reflect a slow turnover of Opa3 protein in vivo and may be important in normal lens physiology. | 21613372 |
| 2010-01-21 00:00:00 | to investigate the OPA3 function we have generated a novel ENU-induced mutant mouse carrying a missense mutation in the OPA3 gene. In the heterozygous state, the mice appear uncompromised. In the homozygous state mice display some of the features of MGA. | 18222992 |
| Type | IDs |
|---|---|
| Synonymous | D630048P19Rik, Gm1425, Gm472 |
| Gene |
UniProtKB-ID:
OPA3_MOUSE
UniprotKB:
Q505D7
UniParc:
UPI0000193F3E
EMBL:
BC094601,
AK164755,
AK133480,
AK170977,
AK052774,
BC132309,
AK154960,
BC132311
Ensembl:
ENSMUSG00000052214
KO:
mmu:403187
|
| Nucleutide sequences |
EMBL-CDS:
BAE32955.1,
BAE42155.1,
BAE37900.1,
AAI32312.1,
BAE21678.1,
BAC35141.1,
AAI32310.1,
AAH94601.1
Ensembl_TRS:
ENSMUST00000063976
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000069965
RefSeq:
NP_997408.2
|
| Others |
UniRef100:
UniRef100_Q505D7
UniRef90:
UniRef90_Q505D7
UniRef50:
UniRef50_Q9H6K4
UniGene:
Mm.239583
CCDS:
CCDS20894.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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