Homo sapiens (human): 509 Help Entry 509               CDS       T01001                                  Symbol ATP5F1C, ATP5C, ATP5C1, ATP5CL1 Name (RefSeq) ATP synthase F1 subunit gamma   KO K02136   F-type H+-transporting ATPase subunit gamma Organism hsa  Homo sapiens (human) Pathway hsa00190   Oxidative phosphorylation hsa01100   Metabolic pathways hsa04714   Thermogenesis hsa05010   Alzheimer disease hsa05012   Parkinson disease hsa05014   Amyotrophic lateral sclerosis hsa05016   Huntington disease hsa05020   Prion disease hsa05022   Pathways of neurodegeneration - multiple diseases hsa05208   Chemical carcinogenesis - reactive oxygen species hsa05415   Diabetic cardiomyopathy Module hsa_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:hsa00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     509 (ATP5F1C)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     509 (ATP5F1C)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     509 (ATP5F1C)   09164 Neurodegenerative disease    05010 Alzheimer disease     509 (ATP5F1C)    05012 Parkinson disease     509 (ATP5F1C)    05014 Amyotrophic lateral sclerosis     509 (ATP5F1C)    05016 Huntington disease     509 (ATP5F1C)    05020 Prion disease     509 (ATP5F1C)    05022 Pathways of neurodegeneration - multiple diseases     509 (ATP5F1C)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     509 (ATP5F1C) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt ACT_4 Motif Other DBs NCBI-GeneID:  509 NCBI-ProteinID:  NP_001001973 OMIM:  108729 HGNC:  833 Ensembl:  ENSG00000165629 Pharos:  P36542(Tbio) UniProt:  P36542 Q8TAS0 Structure PDBPDBj LinkDB All DBs Position 10:7788177..7807801 Genome browser AA seq 298 aa AA seqDB search MFSRAGVAGLSAWTLQPQWIQVRNMATLKDITRRLKSIKNIQKITKSMKMVAAAKYARAE RELKPARIYGLGSLALYEKADIKGPEDKKKHLLIGVSSDRGLCGAIHSSIAKQMKSEVAT LTAAGKEVMLVGIGDKIRGILYRTHSDQFLVAFKEVGRKPPTFGDASVIALELLNSGYEF DEGSIIFNKFRSVISYKTEEKPIFSLNTVASADSMSIYDDIDADVLQNYQEYNLANIIYY SLKESTTSEQSARMTAMDNASKNASEMIDKLTLTFNRTRQAVITKELIEIISGAAALD NT seq 897 nt NT seq  +upstreamnt  +downstreamnt atgttctctcgcgcgggtgtcgctgggctgtcggcctggaccttgcagccgcaatggatt caagttcgaaatatggcaactttgaaagatatcaccaggagactaaagtccatcaaaaac atccagaaaattaccaagtctatgaaaatggtagcggcagcaaaatatgcccgagctgag agagagctgaaaccagctcgaatatatggattgggatctttagctctgtatgaaaaagct gatatcaaggggcctgaagacaagaagaaacacctccttattggtgtgtcctcagatcga ggactgtgtggtgctattcattcctccattgctaaacagatgaaaagcgaggttgctaca ctaacagcagctgggaaagaagttatgcttgttggaattggtgacaaaatcagaggcata ctttataggactcattctgaccagtttctggtggcattcaaagaagtgggaagaaagccc cccacttttggagatgcgtcagtcattgcccttgaattactaaattctggatatgaattt gatgaaggctccatcatctttaataaattcaggtctgtcatctcctataagacagaagaa aagcccatcttttcccttaataccgttgcaagtgctgacagcatgagtatctatgacgat attgatgctgacgtgctgcaaaattaccaagaatacaatctggccaacatcatctactac tctctgaaggagtccaccactagtgagcagagtgccaggatgacagccatggacaatgcc agcaagaatgcttctgagatgattgacaaattgacattgacattcaaccgtacccgccaa gctgtcatcacaaaagagttgattgaaattatctctggtgctgcagctctggattaa

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