KEGG   Homo sapiens (human): 4508Help
Entry
4508              CDS       H.sapiens                              

Gene name ATP6
Definition ATP synthase F0 subunit 6
Orthology K02126  F-type H+-transporting ATPase subunit a [EC:3.6.3.14]
Pathway hsa00190  Oxidative phosphorylation
hsa01100  Metabolic pathways
hsa05010  Alzheimer's disease
hsa05012  Parkinson's disease
hsa05016  Huntington's disease
Disease H00068  Leber optic atrophy
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 OrthologParalogGene clusterGFIT
Motif Pfam: ATP-synt_A
PROSITE: ATPASE_A
Motif
Other DBs NCBI-GI: 251831112
NCBI-GeneID: 4508
OMIM: 516060
HGNC: 7414
UniProt: P00846 Q0ZFE3
Position MT
AA seq 226 aa AA seqDB search
MNENLFASFIAPTILGLPAAVLIILFPPLLIPTSKYLINNRLITTQQWLIKLTSKQMMTM
HNTKGRTWSLMLVSLIIFIATTNLLGLLPHSFTPTTQLSMNLAMAIPLWAGTVIMGFRSK
IKNALAHFLPQGTPTPLIPMLVIIETISLLIQPMALAVRLTANITAGHLLMHLIGSATLA
MSTINLPSTLIIFTILILLTILEIAVALIQAYVFTLLVSLYLHDNT
NT seq 681 nt NT seq  +upstreamnt  +downstreamnt
atgaacgaaaatctgttcgcttcattcattgcccccacaatcctaggcctacccgccgca
gtactgatcattctatttccccctctattgatccccacctccaaatatctcatcaacaac
cgactaatcaccacccaacaatgactaatcaaactaacctcaaaacaaatgataaccata
cacaacactaaaggacgaacctgatctcttatactagtatccttaatcatttttattgcc
acaactaacctcctcggactcctgcctcactcatttacaccaaccacccaactatctata
aacctagccatggccatccccttatgagcgggcacagtgattataggctttcgctctaag
attaaaaatgccctagcccacttcttaccacaaggcacacctacaccccttatccccata
ctagttattatcgaaaccatcagcctactcattcaaccaatagccctggccgtacgccta
accgctaacattactgcaggccacctactcatgcacctaattggaagcgccaccctagca
atatcaaccattaaccttccctctacacttatcatcttcacaattctaattctactgact
atcctagaaatcgctgtcgccttaatccaagcctacgttttcacacttctagtaagcctc
tacctgcacgacaacacataa

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