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Homo sapiens (human): 4710
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Entry
4710 CDS
T01001
Symbol
NDUFB4, B15, CI-B15
Name
(RefSeq) NADH:ubiquinone oxidoreductase subunit B4
KO
K03960
NADH dehydrogenase (ubiquinone) 1 beta subcomplex subunit 4
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_M00147
NADH dehydrogenase (ubiquinone) 1 beta subcomplex
Network
nt06460
Alzheimer disease
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
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
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
4710 (NDUFB4)
09150 Organismal Systems
09156 Nervous system
04723 Retrograde endocannabinoid signaling
4710 (NDUFB4)
09159 Environmental adaptation
04714 Thermogenesis
4710 (NDUFB4)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
4710 (NDUFB4)
09164 Neurodegenerative disease
05010 Alzheimer disease
4710 (NDUFB4)
05012 Parkinson disease
4710 (NDUFB4)
05014 Amyotrophic lateral sclerosis
4710 (NDUFB4)
05016 Huntington disease
4710 (NDUFB4)
05020 Prion disease
4710 (NDUFB4)
05022 Pathways of neurodegeneration - multiple diseases
4710 (NDUFB4)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
4710 (NDUFB4)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
4710 (NDUFB4)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
NDUF_B4
Motif
Other DBs
NCBI-GeneID:
4710
NCBI-ProteinID:
NP_004538
OMIM:
603840
HGNC:
7699
Ensembl:
ENSG00000065518
UniProt:
O95168
Structure
PDB
LinkDB
All DBs
Position
3:120596336..120602507
Genome browser
AA seq
129 aa
AA seq
DB search
MSFPKYKPSSLRTLPETLDPAEYNISPETRRAQAERLAIRAQLKREYLLQYNDPNRRGLI
ENPALLRWAYARTINVYPNFRPTPKNSLMGALCGFGPLIFIYYIIKTERDRKEKLIQEGK
LDRTFHLSY
NT seq
390 nt
NT seq
+upstream
nt +downstream
nt
atgtcgttcccaaagtataagccgtcgagcctgcgcactctgcctgagaccctcgaccca
gccgaatacaacatatctccggaaacccggcgggcgcaagccgagcggttggccataaga
gcccagctgaaacgagagtacctgcttcagtacaacgatcccaaccgccgagggctcatc
gaaaatcctgccttgcttcgttgggcctatgcaagaacaataaatgtctatcctaatttc
agacccactcctaaaaactcactcatgggagctctgtgtggatttgggcccctcatcttc
atttattatattatcaaaactgagagggataggaaagaaaaacttatccaggaaggaaaa
ttggatcgaacatttcacctctcatattaa
DBGET
integrated database retrieval system