KEGG   Homo sapiens (human): 518Help
Entry
518               CDS       H.sapiens                              

Gene name ATP5G3
Definition ATP synthase, H+ transporting, mitochondrial F0 complex, subunit C3
(subunit 9)
Orthology K02128  F-type H+-transporting ATPase subunit c [EC:3.6.3.14]
Pathway hsa00190  Oxidative phosphorylation
hsa01100  Metabolic pathways
hsa05010  Alzheimer's disease
hsa05012  Parkinson's disease
hsa05016  Huntington's disease
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_C
PROSITE: ATPASE_C
Motif
Other DBs NCBI-GI: 50659074
NCBI-GeneID: 518
OMIM: 602736
HGNC: 843
HPRD: 04112
Ensembl: ENSG00000154518
UniProt: P48201
Position 2q31.1
AA seq 142 aa AA seqDB search
MFACAKLACTPSLIRAGSRVAYRPISASVLSRPEASRTGEGSTVFNGAQNGVSQLIQREF
QTSAISRDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYARNPSLKQQLFSYAILG
FALSEAMGLFCLMVAFLILFAM
NT seq 429 nt NT seq  +upstreamnt  +downstreamnt
atgttcgcctgcgccaagctcgcctgcaccccctctctgatccgagctggatccagagtt
gcatacagaccaatttctgcatcagtgttatctcgaccagaggctagtaggactggagag
ggctctacggtatttaatggggcccagaatggtgtgtctcagctaatccaaagggagttt
cagaccagtgcaatcagcagagacattgatactgctgccaaatttattggtgcaggtgct
gcaacagtaggagtggctggttctggtgctggtattggaacagtctttggcagccttatc
attggttatgccagaaacccttcgctgaagcagcagctgttctcatatgctatcctggga
tttgccttgtctgaagctatgggtctcttttgtttgatggttgctttcttgattttgttt
gccatgtaa

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