Homo sapiens (human): 4729
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Entry
4729 CDS
T01001
Symbol
NDUFV2, CI-24k, MC1DN7
Name
(RefSeq) NADH:ubiquinone oxidoreductase core subunit V2
KO
K03943
NADH dehydrogenase (ubiquinone) flavoprotein 2 [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
4729 (NDUFV2)
09150 Organismal Systems
09156 Nervous system
04723 Retrograde endocannabinoid signaling
4729 (NDUFV2)
09159 Environmental adaptation
04714 Thermogenesis
4729 (NDUFV2)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
4729 (NDUFV2)
09164 Neurodegenerative disease
05010 Alzheimer disease
4729 (NDUFV2)
05012 Parkinson disease
4729 (NDUFV2)
05014 Amyotrophic lateral sclerosis
4729 (NDUFV2)
05016 Huntington disease
4729 (NDUFV2)
05020 Prion disease
4729 (NDUFV2)
05022 Pathways of neurodegeneration - multiple diseases
4729 (NDUFV2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
4729 (NDUFV2)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
4729 (NDUFV2)
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)
4729 (NDUFV2)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
2Fe-2S_thioredx
Androglobin_II
Motif
Other DBs
NCBI-GeneID:
4729
NCBI-ProteinID:
NP_066552
OMIM:
600532
HGNC:
7717
Ensembl:
ENSG00000178127
Pharos:
P19404
(Tclin)
UniProt:
P19404
Structure
PDB
LinkDB
All DBs
Position
18:9102699..9134341
Genome browser
AA seq
249 aa
AA seq
DB search
MFFSAALRARAAGLTAHWGRHVRNLHKTVMQNGAGGALFVHRDTPENNPDTPFDFTPENY
KRIEAIVKNYPEGHKAAAVLPVLDLAQRQNGWLPISAMNKVAEVLQVPPMRVYEVATFYT
MYNRKPVGKYHIQVCTTTPCMLRNSDSILEAIQKKLGIKVGETTPDKLFTLIEVECLGAC
VNAPMVQINDNYYEDLTAKDIEEIIDELKAGKIPKPGPRSGRFSCEPAGGLTSLTEPPKG
PGFGVQAGL
NT seq
750 nt
NT seq
+upstream
nt +downstream
nt
atgttcttctccgcggcgctccgggcccgggcggctggcctcaccgcccactggggaaga
catgtaaggaatttgcataagacagttatgcaaaatggagctggaggagctttatttgtg
cacagagatactcctgagaataaccctgatactccatttgatttcacaccagaaaactat
aagaggatagaggcaattgtaaaaaactatccagaaggccataaagcagcagctgttctt
ccagtcctggatttagcccaaaggcagaatgggtggttgcccatctctgctatgaacaag
gttgcagaagttttacaagtacctccaatgagagtatatgaagtagcaactttttataca
atgtataatcgaaagccagttggaaagtatcacattcaggtctgcactactacaccctgc
atgcttcgaaactctgacagcatactggaggccattcagaaaaagcttggaataaaggtt
ggggagactacacctgacaaacttttcactcttatagaagtggaatgtttaggggcctgt
gtgaacgcaccaatggttcaaataaatgacaattactatgaggatttgacagctaaggat
attgaagaaattattgatgagctcaaggctggcaaaatcccaaaaccagggccaaggagt
ggacgcttctcttgtgagccagctggaggtcttacctctttgactgaaccacccaaggga
cctggatttggtgtacaagcaggcctttaa
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integrated database retrieval system