KEGG   Homo sapiens (human): 517Help
Entry
517               CDS       T01001                                 

Gene name
ATP5G2, ATP5A
Definition
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9)
Orthology
K02128  
F-type H+-transporting ATPase subunit c
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
Pfam: 
Motif
Other DBs
NCBI-GI: 
NCBI-GeneID: 
OMIM: 
HGNC: 
HPRD: 
Ensembl: 
Vega: 
UniProt: 
Position
12q13.13
AA seq 157 aa AA seqDB search
MPELILSPATAPHPLKMFACSKFVSTPSLVKSTSQLLSRPLSAVVLKRPEILTDESLSSL
AVSCPLTSLVSSRSFQTSAISRDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYAR
NPSLKQQLFSYAILGFALSEAMGLFCLMVAFLILFAM
NT seq 474 nt NT seq  +upstreamnt  +downstreamnt
atgcctgagctgatcctctctcctgccacagctcctcaccccctgaaaatgttcgcctgc
tccaagtttgtctccactccctccttggtcaagagcacctcacagctgctgagccgtccg
ctatctgcagtggtgctgaaacgaccggagatactgacagatgagagcctcagcagcttg
gcagtctcatgtccccttacctcacttgtctctagccgcagcttccaaaccagcgccatt
tcaagggacatcgacacagcagccaagttcattggagctggggctgccacagttggggtg
gctggttctggggctgggattggaactgtgtttgggagcctcatcattggttatgccagg
aacccttctctgaagcaacagctcttctcctacgccattctgggctttgccctctcggag
gccatggggctcttttgtctgatggtagcctttctcatcctctttgccatgtga

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