KEGG   Homo sapiens (human): 516Help
Entry
516               CDS       H.sapiens                              

Gene name ATP5G1
Definition ATP synthase, H+ transporting, mitochondrial F0 complex, subunit C1
(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: 50659069
NCBI-GeneID: 516
OMIM: 603192
HGNC: 841
HPRD: 04428
Ensembl: ENSG00000159199
UniProt: P05496 Q6FIH7
Position 17q21.32
AA seq 136 aa AA seqDB search
MQTAGALFISPALIRCCTRGLIRPVSASFLNSPVNSSKQPSYSNFPLQVARREFQTSVVS
RDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYARNPSLKQQLFSYAILGFALSEA
MGLFCLMVAFLILFAM
NT seq 411 nt NT seq  +upstreamnt  +downstreamnt
atgcagaccgccggggcattattcatttctccagctctgatccgctgttgtaccaggggt
ctaatcaggcctgtgtctgcctccttcttgaatagcccagtgaattcatctaaacagcct
tcctacagcaacttcccactccaggtggccagacgggagttccagaccagtgttgtctcc
cgggacattgacacagcagccaagtttattggtgctggggcagccacagttggtgtggct
ggttcaggggctggcattggaaccgtgtttggcagcttgatcattggctatgccaggaac
ccgtctctcaagcagcagctcttctcctatgccattcttggctttgccctgtctgaggcc
atggggcttttctgtttgatggtcgccttcctcatcctcttcgccatgtga

DBGET integrated database retrieval system