Homo sapiens (human): 7381
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Entry
7381 CDS
T01001
Symbol
UQCRB, MC3DN3, QCR7, QP-C, QPC, UQBC, UQBP, UQCR6, UQPC
Name
(RefSeq) ubiquinol-cytochrome c reductase binding protein
KO
K00417
ubiquinol-cytochrome c reductase subunit 7
Organism
hsa
Homo sapiens (human)
Pathway
hsa00190
Oxidative phosphorylation
hsa01100
Metabolic pathways
hsa04260
Cardiac muscle contraction
hsa04714
Thermogenesis
hsa04932
Non-alcoholic fatty liver disease
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05208
Chemical carcinogenesis - reactive oxygen species
hsa05415
Diabetic cardiomyopathy
Module
hsa_M00152
Cytochrome bc1 complex
Network
nt06252
Mitochondrial ROS formation (cancer)
nt06461
Huntington disease
nt06463
Parkinson disease
nt06466
Pathways of neurodegeneration
nt06529
Thermogenesis
Element
N00990
Electron transfer in Complex III
N00991
Mutation-caused aberrant Htt to electron transfer in Complex III
N01046
Maneb to electron transfer in Complex III
N01395
Cadmium to electron transfer in complex III
N01691
mitochondrial complex - UCP1 in Thermogenesis
Disease
H02086
Mitochondrial complex III deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
7381 (UQCRB)
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
7381 (UQCRB)
09159 Environmental adaptation
04714 Thermogenesis
7381 (UQCRB)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
7381 (UQCRB)
09164 Neurodegenerative disease
05010 Alzheimer disease
7381 (UQCRB)
05012 Parkinson disease
7381 (UQCRB)
05014 Amyotrophic lateral sclerosis
7381 (UQCRB)
05016 Huntington disease
7381 (UQCRB)
05020 Prion disease
7381 (UQCRB)
05022 Pathways of neurodegeneration - multiple diseases
7381 (UQCRB)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
7381 (UQCRB)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
7381 (UQCRB)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
UCR_14kD
Motif
Other DBs
NCBI-GeneID:
7381
NCBI-ProteinID:
NP_006285
OMIM:
191330
HGNC:
12582
Ensembl:
ENSG00000156467
UniProt:
P14927
Structure
PDB
LinkDB
All DBs
Position
8:complement(96222947..96235545)
Genome browser
AA seq
111 aa
AA seq
DB search
MAGKQAVSASGKWLDGIRKWYYNAAGFNKLGLMRDDTIYEDEDVKEAIRRLPENLYNDRM
FRIKRALDLNLKHQILPKEQWTKYEEENFYLEPYLKEVIRERKEREEWAKK
NT seq
336 nt
NT seq
+upstream
nt +downstream
nt
atggctggtaagcaggccgtttcagcatcaggcaagtggctggatggtattcgaaaatgg
tattacaatgctgcaggattcaataaactggggttaatgcgagatgatacaatatacgag
gatgaagatgtaaaagaagccataagaagacttcctgagaacctttataatgacaggatg
tttcgcattaagagggcactggacctgaacttgaagcatcagatcttgcctaaagagcag
tggaccaaatatgaagaggaaaatttctaccttgaaccgtatctgaaagaggttattcgg
gaaagaaaagaaagagaagaatgggcaaagaagtaa
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