Homo sapiens (human): 513 Help Entry 513               CDS       T01001                                  Symbol ATP5F1D, ATP5D, MC5DN5 Name (RefSeq) ATP synthase F1 subunit delta   KO K02134   F-type H+-transporting ATPase subunit delta 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     513 (ATP5F1D)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     513 (ATP5F1D)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     513 (ATP5F1D)   09164 Neurodegenerative disease    05010 Alzheimer disease     513 (ATP5F1D)    05012 Parkinson disease     513 (ATP5F1D)    05014 Amyotrophic lateral sclerosis     513 (ATP5F1D)    05016 Huntington disease     513 (ATP5F1D)    05020 Prion disease     513 (ATP5F1D)    05022 Pathways of neurodegeneration - multiple diseases     513 (ATP5F1D)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     513 (ATP5F1D) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATPD_C_metazoa ATP-synt_DE_N Motif Other DBs NCBI-GeneID:  513 NCBI-ProteinID:  NP_001001975 OMIM:  603150 HGNC:  837 Ensembl:  ENSG00000099624 UniProt:  P30049 Structure PDBPDBj LinkDB All DBs Position 19:1241751..1244825 Genome browser AA seq 168 aa AA seqDB search MLPAALLRRPGLGRLVRHARAYAEAAAAPAAASGPNQMSFTFASPTQVFFNGANVRQVDV PTLTGAFGILAAHVPTLQVLRPGLVVVHAEDGTTSKYFVSSGSIAVNADSSVQLLAEEAV TLDMLDLGAAKANLEKAQAELVGTADEATRAEIQIRIEANEALVKALE NT seq 507 nt NT seq  +upstreamnt  +downstreamnt atgctgcccgccgcgctgctccgccgcccgggacttggccgcctcgtccgccacgcccgt gcctatgccgaggccgccgccgccccggctgccgcctctggccccaaccagatgtccttc accttcgcctctcccacgcaggtgttcttcaacggtgccaacgtccggcaggtggacgtg cccacgctgaccggagccttcggcatcctggcggcccacgtgcccacgctgcaggtcctg cggccggggctggtcgtggtgcatgcagaggacggcaccacctccaaatactttgtgagc agcggttccatcgcagtgaacgccgactcttcggtgcagttgttggccgaagaggccgtg acgctggacatgttggacctgggggcagccaaggcaaacttggagaaggcccaggcggag ctggtggggacagctgacgaggccacgcgggcagagatccagatccgaatcgaggccaac gaggccctggtgaaggccctggagtag

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