KEGG   Homo sapiens (human): 51079
Entry
51079             CDS       T01001                                 
Symbol
NDUFA13, B16.6, CDA016, CGI-39, GRIM-19, GRIM19, MC1DN28
Name
(RefSeq) NADH:ubiquinone oxidoreductase subunit A13
  KO
K11353  NADH dehydrogenase (ubiquinone) 1 alpha subcomplex subunit 13
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
    51079 (NDUFA13)
 09150 Organismal Systems
  09156 Nervous system
   04723 Retrograde endocannabinoid signaling
    51079 (NDUFA13)
  09159 Environmental adaptation
   04714 Thermogenesis
    51079 (NDUFA13)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    51079 (NDUFA13)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    51079 (NDUFA13)
   05012 Parkinson disease
    51079 (NDUFA13)
   05014 Amyotrophic lateral sclerosis
    51079 (NDUFA13)
   05016 Huntington disease
    51079 (NDUFA13)
   05020 Prion disease
    51079 (NDUFA13)
   05022 Pathways of neurodegeneration - multiple diseases
    51079 (NDUFA13)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    51079 (NDUFA13)
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    51079 (NDUFA13)
SSDB
Motif
Pfam: GRIM-19 COX14 CSTF_C
Other DBs
NCBI-GeneID: 51079
NCBI-ProteinID: NP_057049
OMIM: 609435
HGNC: 17194
Ensembl: ENSG00000186010
UniProt: Q9P0J0
Structure
LinkDB
Position
19:19516225..19528198
AA seq 144 aa
MAASKVKQDMPPPGGYGPIDYKRNLPRRGLSGYSMLAIGIGTLIYGHWSIMKWNRERRRL
QIEDFEARIALLPLLQAETDRRTLQMLRENLEEEAIIMKDVPDWKVGESVFHTTRWVPPL
IGELYGLRTTEEALHASHGFMWYT
NT seq 435 nt   +upstreamnt  +downstreamnt
atggcggcgtcaaaggtgaagcaggacatgcctccgccggggggctatgggcccatcgac
tacaaacggaacttgccgcgtcgaggactgtcgggctacagcatgctggccatagggatt
ggaaccctgatctacgggcactggagcataatgaagtggaaccgtgagcgcaggcgccta
caaatcgaggacttcgaggctcgcatcgcgctgttgccactgttacaggcagaaaccgac
cggaggaccttgcagatgcttcgggagaacctggaggaggaggccatcatcatgaaggac
gtgcccgactggaaggtgggggagtctgtgttccacacaacccgctgggtgccccccttg
atcggggagctgtacgggctgcgcaccacagaggaggctctccatgccagccacggcttc
atgtggtacacgtag

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