Homo sapiens (human): 4724
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Entry
4724 CDS
T01001
Symbol
NDUFS4, AQDQ, CI-18, CI-18_kDa, CI-AQDQ, MC1DN1
Name
(RefSeq) NADH:ubiquinone oxidoreductase subunit S4
KO
K03937
NADH dehydrogenase (ubiquinone) Fe-S protein 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_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
4724 (NDUFS4)
09150 Organismal Systems
09156 Nervous system
04723 Retrograde endocannabinoid signaling
4724 (NDUFS4)
09159 Environmental adaptation
04714 Thermogenesis
4724 (NDUFS4)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
4724 (NDUFS4)
09164 Neurodegenerative disease
05010 Alzheimer disease
4724 (NDUFS4)
05012 Parkinson disease
4724 (NDUFS4)
05014 Amyotrophic lateral sclerosis
4724 (NDUFS4)
05016 Huntington disease
4724 (NDUFS4)
05020 Prion disease
4724 (NDUFS4)
05022 Pathways of neurodegeneration - multiple diseases
4724 (NDUFS4)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
4724 (NDUFS4)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
4724 (NDUFS4)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
NDUS4
CSN8_PSD8_EIF3K
Motif
Other DBs
NCBI-GeneID:
4724
NCBI-ProteinID:
NP_002486
OMIM:
602694
HGNC:
7711
Ensembl:
ENSG00000164258
UniProt:
O43181
A0A0S2Z433
Structure
PDB
PDBj
LinkDB
All DBs
Position
5:53560639..53683338
Genome browser
AA seq
175 aa
AA seq
DB search
MAAVSMSVVLRQTLWRRRAVAVAALSVSRVPTRSLRTSTWRLAQDQTQDTQLITVDEKLD
ITTLTGVPEEHIKTRKVRIFVPARNNMQSGVNNTKKWKMEFDTRERWENPLMGWASTADP
LSNMVLTFSTKEDAVSFAEKNGWSYDIEERKVPKPKSKSYGANFSWNKRTRVSTK
NT seq
528 nt
NT seq
+upstream
nt +downstream
nt
atggcggcggtgtcaatgtcagtggtactgaggcagacgttgtggcggagaagggcagtg
gctgtagctgccctttccgtttccagggttccgaccaggtcgttgaggacttccacatgg
agattggcacaggaccagactcaagacacacaactcataacagttgatgaaaaattggat
atcactactttaactggagttccagaagagcatataaaaactagaaaagtcaggatcttt
gttcctgctcgcaataacatgcagtctggagtaaacaacacaaagaaatggaagatggag
tttgataccagagagcgatgggaaaatcctttgatgggttgggcatcaacggctgatccc
ttatccaacatggttctaaccttcagtactaaagaagatgcagtttcctttgcagaaaaa
aatggatggagctatgacattgaagagaggaaggttccaaaacccaagtccaagtcttat
ggtgcaaacttttcttggaacaaaagaacaagagtatccacaaaatag
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integrated database retrieval system