KEGG   Homo sapiens (human): 29796
Entry
29796             CDS       T01001                                 
Symbol
UQCR10, HSPC051, HSPC119, HSPC151, QCR9, UCCR7.2, UCRC
Name
(RefSeq) ubiquinol-cytochrome c reductase, complex III subunit X
  KO
K00419  ubiquinol-cytochrome c reductase subunit 9
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
  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
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    29796 (UQCR10)
 09150 Organismal Systems
  09153 Circulatory system
   04260 Cardiac muscle contraction
    29796 (UQCR10)
  09159 Environmental adaptation
   04714 Thermogenesis
    29796 (UQCR10)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    29796 (UQCR10)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    29796 (UQCR10)
   05012 Parkinson disease
    29796 (UQCR10)
   05014 Amyotrophic lateral sclerosis
    29796 (UQCR10)
   05016 Huntington disease
    29796 (UQCR10)
   05020 Prion disease
    29796 (UQCR10)
   05022 Pathways of neurodegeneration - multiple diseases
    29796 (UQCR10)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    29796 (UQCR10)
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    29796 (UQCR10)
SSDB
Motif
Pfam: UCR_UQCRX_QCR9
Other DBs
NCBI-GeneID: 29796
NCBI-ProteinID: NP_037519
OMIM: 610843
HGNC: 30863
Ensembl: ENSG00000184076
UniProt: Q9UDW1
Structure
LinkDB
Position
22:29767369..29770413
AA seq 63 aa
MAAATLTSKLYSLLFRRTSTFALTIIVGVMFFERAFDQGADAIYDHINEGKLWKHIKHKY
ENK
NT seq 192 nt   +upstreamnt  +downstreamnt
atggcggccgcgacgttgacttcgaaattgtactccctgctgttccgcaggacctccacc
ttcgccctcaccatcatcgtgggcgtcatgttcttcgagcgcgccttcgatcaaggcgcg
gacgctatctacgaccacatcaacgaggggaagctgtggaaacacatcaagcacaagtat
gagaacaagtag

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