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Homo sapiens (human): 374291
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Entry
374291 CDS
T01001
Symbol
NDUFS7, CI-20, CI-20KD, MC1DN3, MY017, PSST
Name
(RefSeq) NADH:ubiquinone oxidoreductase core subunit S7
KO
K03940
NADH dehydrogenase (ubiquinone) Fe-S protein 7 [EC:
7.1.1.2
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa00190
Oxidative phosphorylation
hsa01100
Metabolic pathways
hsa04714
Thermogenesis
hsa04723
Retrograde endocannabinoid signaling
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_M00143
NADH dehydrogenase (ubiquinone) Fe-S protein/flavoprotein complex, mitochondria
Network
nt06460
Alzheimer disease
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06529
Thermogenesis
Element
N00995
Electron transfer in Complex I
N00997
Mutation-caused aberrant Abeta to electron transfer in Complex I
N01042
Mutation-caused aberrant SNCA to electron transfer in Complex I
N01043
Mutation-inactivated PINK1 to electron transfer in Complex I
N01044
MPP+ to electron transfer in Complex I
N01045
Rotenone to electron transfer in Complex I
N01136
Mutation-caused aberrant TDP43 to electron transfer in Complex I
N01691
mitochondrial complex - UCP1 in Thermogenesis
Disease
H00473
Mitochondrial complex I deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
374291 (NDUFS7)
09150 Organismal Systems
09156 Nervous system
04723 Retrograde endocannabinoid signaling
374291 (NDUFS7)
09159 Environmental adaptation
04714 Thermogenesis
374291 (NDUFS7)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
374291 (NDUFS7)
09164 Neurodegenerative disease
05010 Alzheimer disease
374291 (NDUFS7)
05012 Parkinson disease
374291 (NDUFS7)
05014 Amyotrophic lateral sclerosis
374291 (NDUFS7)
05016 Huntington disease
374291 (NDUFS7)
05020 Prion disease
374291 (NDUFS7)
05022 Pathways of neurodegeneration - multiple diseases
374291 (NDUFS7)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
374291 (NDUFS7)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
374291 (NDUFS7)
Enzymes [BR:
hsa01000
]
7. Translocases
7.1 Catalysing the translocation of protons
7.1.1 Linked to oxidoreductase reactions
7.1.1.2 NADH:ubiquinone reductase (H+-translocating)
374291 (NDUFS7)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Oxidored_q6
Secapin
Motif
Other DBs
NCBI-GeneID:
374291
NCBI-ProteinID:
NP_077718
OMIM:
601825
HGNC:
7714
Ensembl:
ENSG00000115286
Pharos:
O75251
(Tclin)
UniProt:
O75251
Q7LD69
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:1383907..1395584
Genome browser
AA seq
213 aa
AA seq
DB search
MAVLSAPGLRGFRILGLRSSVGPAVQARGVHQSVATDGPSSTQPALPKARAVAPKPSSRG
EYVVAKLDDLVNWARRSSLWPMTFGLACCAVEMMHMAAPRYDMDRFGVVFRASPRQSDVM
IVAGTLTNKMAPALRKVYDQMPEPRYVVSMGSCANGGGYYHYSYSVVRGCDRIVPVDIYI
PGCPPTAEALLYGILQLQRKIKRERRLQIWYRR
NT seq
642 nt
NT seq
+upstream
nt +downstream
nt
atggcggtgctgtcagctcctggcctgcgcggcttccggatccttggtctgcgctccagc
gtgggcccggctgtgcaggcacgaggtgtccatcagagcgtggccaccgatggcccaagc
agcacccagcctgccctgccaaaggccagagccgtggctcccaaacccagcagccggggc
gagtatgtggtggccaagctggatgacctcgtcaactgggcccgccggagttctctgtgg
cccatgaccttcggcctggcctgctgcgccgtggagatgatgcacatggcagcaccccgc
tacgacatggaccgctttggcgtggtcttccgcgccagcccgcgccagtccgacgtcatg
atcgtggccggcacactcaccaacaagatggccccagcgcttcgcaaggtctacgaccag
atgccggagccgcgctacgtggtctccatggggagctgcgccaacggaggaggctactac
cactattcctactcggtggtgaggggctgcgaccgcatcgtgcccgtggacatctacatc
ccaggctgcccacctacggccgaggccctgctctacggcatcctgcagctgcagaggaag
atcaagcgggagcggaggctgcagatctggtaccgcaggtag
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