Homo sapiens (human): 514 Help Entry 514               CDS       T01001                                  Symbol ATP5F1E, ATP5E, ATPE, MC5DN3 Name (RefSeq) ATP synthase F1 subunit epsilon   KO K02135   F-type H+-transporting ATPase subunit epsilon 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 Network nt06529  Thermogenesis   Element N01691   mitochondrial complex - UCP1 in Thermogenesis Disease H01369   ATP synthase deficiency Brite KEGG Orthology (KO) [BR:hsa00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     514 (ATP5F1E)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     514 (ATP5F1E)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     514 (ATP5F1E)   09164 Neurodegenerative disease    05010 Alzheimer disease     514 (ATP5F1E)    05012 Parkinson disease     514 (ATP5F1E)    05014 Amyotrophic lateral sclerosis     514 (ATP5F1E)    05016 Huntington disease     514 (ATP5F1E)    05020 Prion disease     514 (ATP5F1E)    05022 Pathways of neurodegeneration - multiple diseases     514 (ATP5F1E)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     514 (ATP5F1E) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_Eps Motif Other DBs NCBI-GeneID:  514 NCBI-ProteinID:  NP_008817 OMIM:  606153 HGNC:  838 Ensembl:  ENSG00000124172 Pharos:  P56381(Tbio) UniProt:  P56381 Structure PDBPDBj LinkDB All DBs Position 20:complement(59025475..59032335) Genome browser AA seq 51 aa AA seqDB search MVAYWRQAGLSYIRYSQICAKAVRDALKTEFKANAEKTSGSNVKIVKVKKE NT seq 156 nt NT seq  +upstreamnt  +downstreamnt atggtggcctactggagacaggctggactcagctacatccgatactcccagatctgtgca aaagcagtgagagatgcactgaagacagaattcaaagcaaatgctgagaagacttctggc agcaacgtaaaaattgtgaaagtaaagaaggaataa

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