KEGG   Homo sapiens (human): 10476Help
Entry
10476             CDS       T01001                                 
Gene name
ATP5H, ATPQ
Definition
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d (EC:3.6.1.14)
Orthology
K02138  
F-type H+-transporting ATPase subunit d [EC:3.6.3.14]
Organism
hsa  Homo sapiens (human)
Pathway
Oxidative phosphorylation
Metabolic pathways
Alzheimer's disease
Parkinson's disease
Huntington's disease
Module
F-type ATPase, eukaryotes
Class
Metabolism; Energy metabolism; Oxidative phosphorylation [PATH:hsa00190]
Human Diseases; Neurodegenerative diseases; Alzheimer's disease [PATH:hsa05010]
Human Diseases; Neurodegenerative diseases; Parkinson's disease [PATH:hsa05012]
Human Diseases; Neurodegenerative diseases; Huntington's disease [PATH:hsa05016]
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif Motif
Other DBs
NCBI-GI: 
NCBI-GeneID: 
HGNC: 
HPRD: 
Ensembl: 
Vega: 
UniProt: 
Position
17q25
AA seq 137 aa AA seqDB search
MAGRKLALKTIDWVAFAEIIPQNQKAIASSLKSWNETLTSRLAALPENPPAIDWAYYKAN
VAKAGLVDDFEKKVKSCAEWVSLSKARIVEYEKEMEKMKNLIPFDQMTIEDLNEAFPETK
LDKKKYPYWPHQPIENL
NT seq 414 nt NT seq  +upstreamnt  +downstreamnt
atggctgggcgaaaacttgctctaaaaaccattgactgggtagcttttgcagagatcata
ccccagaaccaaaaggccattgctagttccctgaaatcctggaatgagaccctcacctcc
aggttggctgctttacctgagaatccaccagctatcgactgggcttactacaaggccaat
gtggccaaggctggcttggtggatgactttgagaagaaggtgaaatcttgtgctgagtgg
gtgtctctctcaaaggccaggattgtagaatatgagaaagagatggagaagatgaagaac
ttaattccatttgatcagatgaccattgaggacttgaatgaagctttcccagaaaccaaa
ttagacaagaaaaagtatccctattggcctcaccaaccaattgagaatttataa
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