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Homo sapiens (human): 4694
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Entry
4694 CDS
T01001
Symbol
NDUFA1, CI-MWFE, MC1DN12, MWFE, ZNF183
Name
(RefSeq) NADH:ubiquinone oxidoreductase subunit A1
KO
K03945
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex subunit 1
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_M00146
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex
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
4694 (NDUFA1)
09150 Organismal Systems
09156 Nervous system
04723 Retrograde endocannabinoid signaling
4694 (NDUFA1)
09159 Environmental adaptation
04714 Thermogenesis
4694 (NDUFA1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
4694 (NDUFA1)
09164 Neurodegenerative disease
05010 Alzheimer disease
4694 (NDUFA1)
05012 Parkinson disease
4694 (NDUFA1)
05014 Amyotrophic lateral sclerosis
4694 (NDUFA1)
05016 Huntington disease
4694 (NDUFA1)
05020 Prion disease
4694 (NDUFA1)
05022 Pathways of neurodegeneration - multiple diseases
4694 (NDUFA1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
4694 (NDUFA1)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
4694 (NDUFA1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MWFE
Motif
Other DBs
NCBI-GeneID:
4694
NCBI-ProteinID:
NP_004532
OMIM:
300078
HGNC:
7683
Ensembl:
ENSG00000125356
UniProt:
O15239
Q6IBB5
Structure
PDB
LinkDB
All DBs
Position
X:119871832..119876662
Genome browser
AA seq
70 aa
AA seq
DB search
MWFEILPGLSVMGVCLLIPGLATAYIHRFTNGGKEKRVAHFGYHWSLMERDRRISGVDRY
YVSKGLENID
NT seq
213 nt
NT seq
+upstream
nt +downstream
nt
atgtggttcgagattctccccggactctccgtcatgggcgtgtgcttgttgattccagga
ctggctactgcgtacatccacaggttcactaacgggggcaaggaaaaaagggttgctcat
tttgggtatcactggagtctgatggaaagagataggcgcatctctggagttgatcgttac
tatgtgtcaaagggtttggagaacattgattaa
DBGET
integrated database retrieval system