Homo sapiens (human): 80207
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Entry
80207 CDS
T01001
Symbol
OPA3, MGA3
Name
(RefSeq) outer mitochondrial membrane lipid metabolism regulator OPA3
KO
K23166
optic atrophy 3 protein
Organism
hsa
Homo sapiens (human)
Disease
H00754
3-Methylglutaconic aciduria
H01020
Optic atrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
80207 (OPA3)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitochondrial dynamics
Fission and Fusion factors
80207 (OPA3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
OPA3
DUF2730
Cep57_MT_bd
RM2_Med14
DUF6779
Motif
Other DBs
NCBI-GeneID:
80207
NCBI-ProteinID:
NP_079412
OMIM:
606580
HGNC:
8142
Ensembl:
ENSG00000125741
UniProt:
Q9H6K4
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All DBs
Position
19:complement(45527427..45584802)
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AA seq
179 aa
AA seq
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MVVGAFPMAKLLYLGIRQVSKPLANRIKEAARRSEFFKTYICLPPAQLYHWVEMRTKMRI
MGFRGTVIKPLNEEAAAELGAELLGEATIFIVGGGCLVLEYWRHQAQQRHKEEEQRAAWN
ALRDEVGHLALALEALQAQVQAAPPQGALEELRTELQEVRAQLCNPGRSASHAVPASKK
NT seq
540 nt
NT seq
+upstream
nt +downstream
nt
atggtggtgggcgcgttccctatggcgaagctgctatacttgggcatccggcaggtcagc
aagccgcttgccaaccgtattaaggaggccgcccgccgaagcgagttcttcaagacctat
atctgcctcccgccggctcaactgtatcactgggtggagatgcggaccaagatgcgcatc
atgggcttccggggcacggtcatcaagccgctgaacgaggaggcggcagctgagctgggc
gcagagctgctgggcgaagccaccatcttcatcgtgggcggcggctgcctagtgctggag
tactggcgccaccaggcgcagcagcgccacaaggaggaggagcagcgtgctgcctggaac
gcgctgcgggacgaggtgggccacctggcgctggcgctggaagcgctgcaggcgcaggtg
caggcggcgccgccacagggcgccctggaggaactgcgcacagagctgcaagaggtgcgc
gcccagctctgcaatcccggccggtccgcttcccacgcagtgcctgcgtccaagaaatag
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integrated database retrieval system
