Homo sapiens (human): 790955
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Entry
790955 CDS
T01001
Symbol
UQCC3, C11orf83, CCDS41658.1, MC3DN9, UNQ655
Name
(RefSeq) ubiquinol-cytochrome-c reductase complex assembly factor 3
KO
K23165
ubiquinol-cytochrome-c reductase complex assembly factor 3
Organism
hsa
Homo sapiens (human)
Disease
H02086
Mitochondrial complex III deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
790955 (UQCC3)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitochondrial respiratory chain complex assembly factors
Complex-III assembly factors
790955 (UQCC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
UQCC3
Motif
Other DBs
NCBI-GeneID:
790955
NCBI-ProteinID:
NP_001078841
OMIM:
616097
HGNC:
34399
Ensembl:
ENSP00000367189.3
UniProt:
Q6UW78
LinkDB
All DBs
Position
11:62671673..62673686
Genome browser
AA seq
93 aa
AA seq
DB search
MDSLRKMLISVAMLGAGAGVGYALLVIVTPGERRKQEMLKEMPLQDPRSREEAARTQQLL
LATLQEAATTQENVAWRKNWMVGGEGGAGGRSP
NT seq
282 nt
NT seq
+upstream
nt +downstream
nt
atggattccttgcggaaaatgctgatctcagtcgcaatgctgggcgcaggggctggcgtg
ggctacgcgctcctcgttatcgtgaccccgggagagcggcggaagcaggaaatgctaaag
gagatgccactgcaggacccaaggagcagggaggaggcggccaggacccagcagctattg
ctggccactctgcaggaggcagcgaccacgcaggagaacgtggcctggaggaagaactgg
atggttggcggcgaaggcggcgccggcgggaggtcaccgtga
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