Rattus norvegicus (rat): 114630 Help Entry 114630            CDS       T01003                                  Symbol Atp5mc3 Name (RefSeq) ATP synthase F(0) complex subunit C3, mitochondrial precursor   KO K02128   F-type H+-transporting ATPase subunit c Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     114630 (Atp5mc3)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     114630 (Atp5mc3)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     114630 (Atp5mc3)   09164 Neurodegenerative disease    05010 Alzheimer disease     114630 (Atp5mc3)    05012 Parkinson disease     114630 (Atp5mc3)    05014 Amyotrophic lateral sclerosis     114630 (Atp5mc3)    05016 Huntington disease     114630 (Atp5mc3)    05020 Prion disease     114630 (Atp5mc3)    05022 Pathways of neurodegeneration - multiple diseases     114630 (Atp5mc3)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     114630 (Atp5mc3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_C Motif Other DBs NCBI-GeneID:  114630 NCBI-ProteinID:  NP_001348329 RGD:  620052 Ensembl:  ENSRNOG00000001596 LinkDB All DBs Position 3:complement(58810535..58813185) Genome browser AA seq 141 aa AA seqDB search MFACAKLARTPALIRAGSRVAYRPISASVLSRPETRTGEGSTVFNGAQNGVCQLIRREFQ TSVISRDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYARNPSLKQQLFSYAILGF ALSEAMGLFCLMVAFLILFAM NT seq 426 nt NT seq  +upstreamnt  +downstreamnt atgttcgcctgcgccaagctcgcccgcacccctgctctgatccgagctggatccagagtt gcatatagaccaatttctgcatcagtattatctcgaccagagactaggactggagagggc tctacggtatttaatggggcccagaatggtgtgtgccagctgatccgaagggagttccag accagtgtaatcagcagagatattgatactgctgccaaattcattggtgcaggtgctgcc acagtaggagttgctggttctggtgctggtattggaacagtctttggcagtcttatcatt ggctatgccagaaacccttcactgaagcagcagctgttctcatacgctatcctgggattt gccttgtctgaagctatgggtctcttttgtttgatggttgcgttcttgatcttgtttgcc atgtaa

Rattus norvegicus (rat): 116550 Help Entry 116550            CDS       T01003                                  Symbol Atp5f1c Name (RefSeq) ATP synthase subunit gamma, mitochondrial   KO K02136   F-type H+-transporting ATPase subunit gamma Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     116550 (Atp5f1c)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     116550 (Atp5f1c)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     116550 (Atp5f1c)   09164 Neurodegenerative disease    05010 Alzheimer disease     116550 (Atp5f1c)    05012 Parkinson disease     116550 (Atp5f1c)    05014 Amyotrophic lateral sclerosis     116550 (Atp5f1c)    05016 Huntington disease     116550 (Atp5f1c)    05020 Prion disease     116550 (Atp5f1c)    05022 Pathways of neurodegeneration - multiple diseases     116550 (Atp5f1c)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     116550 (Atp5f1c) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt ACT_4 Motif Other DBs NCBI-GeneID:  116550 NCBI-ProteinID:  NP_446277 RGD:  620011 Ensembl:  ENSRNOG00000019223 UniProt:  Q6PCU0 LinkDB All DBs Position 17:68423927..68446169 Genome browser AA seq 298 aa AA seqDB search MFSRASIVGLSACSLQPQWIQVRNMATLKDITRRLKSIKNIQKITKSMKMVAAAKYARAE RELKPARVYGTGSLALYEKAEIKGPEDKKKHLIIGVSSDRGLCGAIHSSVAKQMKNDMAA LTAAGKEVMIVGIGEKIKSILYRTHSDQFLVSFKDVGRKPPTFGDASVIALELLNSGYEF DEGSIIFNQFKSVISYKTEEKPIFSFSTVVAAENMSIYDDIDADVLQNYQEYNLANIIYY SLKESTTSEQSARMTAMDNASKNASDMIDKLTLTFNRTRQAVITKELIEIISGAAALD NT seq 897 nt NT seq  +upstreamnt  +downstreamnt atgttctcgcgggcgagtattgtcgggctgtcggcctgctccttgcagccgcaatggatc caagttcgaaacatggcaaccctgaaagacattaccaggagactgaagtccatcaaaaac atccagaagattaccaagtctatgaagatggtggcagcagcgaagtacgcccgggctgag cgggagctgaagccagctcgagtgtatgggacaggctccttggctctgtatgagaaggct gagattaagggacctgaggacaagaagaagcacctcattattggtgtgtcctcggatcga ggcctttgtggtgctattcattcctccgtggctaaacaaatgaagaatgacatggctgcc ctcacagcagctgggaaagaagttatgattgttggaattggtgaaaaaatcaagagcata ctttataggactcactctgatcagtttttggtgtccttcaaagacgtggggcggaagccc cctacttttggagatgcatcggtcattgccttggagttgttaaattcgggatatgaattt gatgaaggctctattatctttaatcagttcaagtctgttatctcctacaagacagaagag aagcccatcttctctttcagtaccgtcgtggctgctgagaacatgagcatttatgatgac attgatgctgacgtgctgcagaattaccaggaatacaatctggccaacatcatctactac tccctgaaggagtccaccaccagtgagcagagtgccaggatgaccgccatggacaacgcc agcaagaacgcctctgatatgattgataaattgacgctgactttcaaccgcacccgccag gccgtcatcacgaaggagctgatagagatcatctccggggctgctgctctggattaa

Rattus norvegicus (rat): 171082 Help Entry 171082            CDS       T01003                                  Symbol Atp5mc2 Name (RefSeq) ATP synthase F(0) complex subunit C2, mitochondrial precursor   KO K02128   F-type H+-transporting ATPase subunit c Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     171082 (Atp5mc2)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     171082 (Atp5mc2)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     171082 (Atp5mc2)   09164 Neurodegenerative disease    05010 Alzheimer disease     171082 (Atp5mc2)    05012 Parkinson disease     171082 (Atp5mc2)    05014 Amyotrophic lateral sclerosis     171082 (Atp5mc2)    05016 Huntington disease     171082 (Atp5mc2)    05020 Prion disease     171082 (Atp5mc2)    05022 Pathways of neurodegeneration - multiple diseases     171082 (Atp5mc2)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     171082 (Atp5mc2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_C Motif Other DBs NCBI-GeneID:  171082 NCBI-ProteinID:  NP_598240 RGD:  620051 Ensembl:  ENSRNOG00000015320 UniProt:  Q06646 LinkDB All DBs Position 7:complement(133791341..133799713) Genome browser AA seq 141 aa AA seqDB search MYACSKFVSTRSLIRSTSQLLSRPLSAVELKRPQMPTDEGLSCLAVRRPLTSLIPSRSFQ TSAISRDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYARNPSLKQQLFSYAILGF ALSEAMGLFCLMVAFLILFAM NT seq 426 nt NT seq  +upstreamnt  +downstreamnt atgtatgcctgctccaagttcgtctctacccgctccctgatcaggagcacctctcagctg ctgagccgtccgctctctgcagtggagttaaagcgaccacagatgcccacagatgagggc ctcagctgcttggcagtccggcggcctctgacctcgcttatccctagccgcagcttccaa accagcgccatttcaagggacattgacacagctgccaagttcattggagctggggctgct acagttggggtggccggttctggagcaggaattgggactgtttttgggagtctcatcatt ggctatgccaggaacccctctctgaagcagcaactcttctcctatgcgattctgggcttc gccctctctgaggccatggggctcttttgcctaatggtggccttcctcatcctcttcgcc atgtga

Rattus norvegicus (rat): 171374 Help Entry 171374            CDS       T01003                                  Symbol Atp5f1b Name (RefSeq) ATP synthase subunit beta, mitochondrial precursor   KO K02133   F-type H+-transporting ATPase subunit beta [EC:7.1.2.2] Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     171374 (Atp5f1b)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     171374 (Atp5f1b)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     171374 (Atp5f1b)   09164 Neurodegenerative disease    05010 Alzheimer disease     171374 (Atp5f1b)    05012 Parkinson disease     171374 (Atp5f1b)    05014 Amyotrophic lateral sclerosis     171374 (Atp5f1b)    05016 Huntington disease     171374 (Atp5f1b)    05020 Prion disease     171374 (Atp5f1b)    05022 Pathways of neurodegeneration - multiple diseases     171374 (Atp5f1b)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     171374 (Atp5f1b) Enzymes [BR:rno01000]  7. Translocases   7.1  Catalysing the translocation of hydrons    7.1.2  Linked to the hydrolysis of a nucleoside triphosphate     7.1.2.2  H+-transporting two-sector ATPase      171374 (Atp5f1b) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_ab ATP-synt_ab_N ATPase_2 NB-ARC RsgA_GTPase ATPase NACHT AAA_16 AAA_19 ABC_tran DUF5832 DUF2075 Motif Other DBs NCBI-GeneID:  171374 NCBI-ProteinID:  NP_599191 RGD:  621368 Ensembl:  ENSRNOG00000002840 UniProt:  P10719 Structure PDB LinkDB All DBs Position 7:515454..521858 Genome browser AA seq 529 aa AA seqDB search MLSLVGRVASASASGALRGLNPLAALPQAHLLLRTAPAGVHPARDYAAQSSAAPKAGTAT GQIVAVIGAVVDVQFDEGLPPILNALEVQGRESRLVLEVAQHLGESTVRTIAMDGTEGLV RGQKVLDSGAPIKIPVGPETLGRIMNVIGEPIDERGPIKTKQFAPIHAEAPEFIEMSVEQ EILVTGIKVVDLLAPYAKGGKIGLFGGAGVGKTVLIMELINNVAKAHGGYSVFAGVGERT REGNDLYHEMIESGVINLKDATSKVALVYGQMNEPPGARARVALTGLTVAEYFRDQEGQD VLLFIDNIFRFTQAGSEVSALLGRIPSAVGYQPTLATDMGTMQERITTTKKGSITSVQAI YVPADDLTDPAPATTFAHLDATTVLSRAIAELGIYPAVDPLDSTSRIMDPNIVGSEHYDV ARGVQKILQDYKSLQDIIAILGMDELSEEDKLTVSRARKIQRFLSQPFQVAEVFTGHMGK LVPLKETIKGFQQILAGDYDHLPEQAFYMVGPIEEAVAKADKLAEEHGS NT seq 1590 nt NT seq  +upstreamnt  +downstreamnt atgttgagtcttgtggggcgtgtggcctcggcctcggcctccggggccttacggggactc aaccctttggcggcgctgccacaggcgcatcttctactacgaaccgctcccgccggggtc catcctgccagagactatgcggcgcagtcgtctgcggccccgaaggcaggcaccgccacc gggcaaattgtggcagtcatcggcgccgttgtggatgtccagttcgatgagggattacca cctatcctaaatgccttggaagtgcaaggcagggagagcagactggttttggaggtagcc cagcatttaggggagagcaccgtcagaactattgctatggatggcactgaaggcttggtt agaggccagaaagtactggattcgggggcaccaatcaaaattcctgttggtcctgagacc ttgggcagaatcatgaatgtcattggagaacctattgatgagagaggtcctatcaaaacc aaacaattcgctcctattcatgctgaggctcctgaattcatagagatgagtgttgaacag gaaattctggtgactggtataaaggttgtggatctgctggccccatacgccaagggtggg aaaatcggactcttcggaggtgctggtgttggaaagacagtactgatcatggagctaatc aacaatgttgctaaagcccatggtggttattctgtatttgctggtgttggtgagaggacc cgtgagggcaatgatttataccatgaaatgattgagtctggtgttatcaacctaaaagat gccacttccaaggtagcgttggtatatgggcagatgaatgaaccgcctggtgctcgtgcc cgggtagctctgactggtctgactgttgctgaatacttcagagaccaggaaggccaagat gtcctgctgtttattgacaacatcttccgcttcacccaggctggctcagaggtatctgcc ttattgggcaggatcccgtctgctgtaggctaccagcctaccctagccactgacatgggt acaatgcaggaaagaatcaccaccaccaagaagggctcgatcacctcagtgcaggctatc tatgtgccagctgatgacctgactgaccctgcccctgcaactacctttgcccatttggat gctactactgtgctgtcccgtgctattgctgagttgggcatctatccagctgtggatcca ctggactccacctctcgaattatggatcccaacatcgttggcagtgagcattatgatgtt gctcgtggggtgcaaaagatcctgcaggactacaaatctctccaggacatcattgccatc ttgggtatggatgaactttctgaggaagataaattgactgtgtccagggcaaggaagata cagcgcttcttgtcacagccattccaggttgctgaggtcttcacaggtcacatgggaaag ctggtgcccctgaaggagaccattaaaggattccagcagatcttagcaggtgactatgac catctcccggaacaagccttctacatggtgggacccattgaagaagctgtggcaaaggct gacaagctggcagaggagcatgggtcgtga

Rattus norvegicus (rat): 171375 Help Entry 171375            CDS       T01003                                  Symbol Atp5pb Name (RefSeq) ATP synthase F(0) complex subunit B1, mitochondrial precursor   KO K02127   F-type H+-transporting ATPase subunit b Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     171375 (Atp5pb)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     171375 (Atp5pb)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     171375 (Atp5pb)   09164 Neurodegenerative disease    05010 Alzheimer disease     171375 (Atp5pb)    05012 Parkinson disease     171375 (Atp5pb)    05014 Amyotrophic lateral sclerosis     171375 (Atp5pb)    05016 Huntington disease     171375 (Atp5pb)    05020 Prion disease     171375 (Atp5pb)    05022 Pathways of neurodegeneration - multiple diseases     171375 (Atp5pb)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     171375 (Atp5pb) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mt_ATP-synt_B TraQ DUF5752 DUF4423 DUF2105 Lambda_Kil Motif Other DBs NCBI-GeneID:  171375 NCBI-ProteinID:  NP_599192 RGD:  620041 Ensembl:  ENSRNOG00000046299 Vega:  OTTRNOG00000000721 UniProt:  P19511 LinkDB All DBs Position 2:complement(193424138..193435418) Genome browser AA seq 256 aa AA seqDB search MLSRVVLSAAATAAPCLKNAAVLGPGVLQATRVFHTGQPRLAPLPPLPEYGGKVRLGLIP EEFFQFLYPKTGVTGPYVLGTGLSLYFLSKEIYVITPETFSTISVVGLIVYVIKKYGASI GEFIDKLNEEKIAQLEEIKQSSMKQIQDAINREKAQQALVQKRHYLFDVQRNNIALALEV TYRERLHKAYKEVKNRLDYHISVQDMMRRKEGEHMINWVEKHVIQSISAQQEKETIAKCI GDLKMLAKKAQAQPIM NT seq 771 nt NT seq  +upstreamnt  +downstreamnt atgctgtcccgggtggtactttctgccgccgccacagcggccccgtgtctgaagaacgcg gccgtcctgggtccaggggttttacaggcaacaagggtctttcacacaggacagcctcgc cttgcccctctaccacctcttcctgaatatggaggaaaagtacgtcttgggctgattcct gaggaatttttccagttcctttaccctaagactggtgtaacaggaccctacgtgcttgga actgggcttagcttgtactttctatccaaagaaatatatgtgattaccccagagaccttc tctaccatatcagtagtagggttgattgtctatgtgattaagaaatatggcgcctctatt ggagaatttattgacaaacttaatgaggaaaaaattgctcaactagaagaaataaagcag tcaagcatgaagcaaatccaggatgcaatcaacagggagaaggcacagcaggcactggtt cagaagcgccactacctcttcgatgttcagaggaataacattgccctggccttggaggtc acttaccgggaacgactacataaagcatataaggaggtaaagaatcgcctggactaccat atttctgtacaggacatgatgcgtcgcaaggagggagagcacatgataaactgggtggag aagcatgtgatacagagcatttctgcacagcaggaaaaggagaccattgccaagtgcatc ggagatctaaagatgcttgcaaagaaggctcaagctcagccaattatgtga

Rattus norvegicus (rat): 192241 Help Entry 192241            CDS       T01003                                  Symbol Atp5po Name (RefSeq) ATP synthase subunit O, mitochondrial precursor   KO K02137   F-type H+-transporting ATPase subunit O Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     192241 (Atp5po)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     192241 (Atp5po)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     192241 (Atp5po)   09164 Neurodegenerative disease    05010 Alzheimer disease     192241 (Atp5po)    05012 Parkinson disease     192241 (Atp5po)    05014 Amyotrophic lateral sclerosis     192241 (Atp5po)    05016 Huntington disease     192241 (Atp5po)    05020 Prion disease     192241 (Atp5po)    05022 Pathways of neurodegeneration - multiple diseases     192241 (Atp5po)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     192241 (Atp5po) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  OSCP Motif Other DBs NCBI-GeneID:  192241 NCBI-ProteinID:  NP_620238 RGD:  621379 Ensembl:  ENSRNOG00000001991 UniProt:  Q06647 LinkDB All DBs Position 11:complement(31165218..31171530) Genome browser AA seq 213 aa AA seqDB search MAAPATSVLSRQVRSFSTSVVRPFSKLVRPPVQVYGIEGRYATALYSAASKQKRLDQVEK ELLRVGQLLKDPKVSLAVLNPYIKRSIKVKSLKDITTKEKFSPLTANLMNLLAENGRLGN TQGVISAFSTIMSVHRGEVPCTVTTAFPLDEAVLSELKTVLNSFLSKGQILNLEVKTDPS IMGGMIVRIGEKYVDMSAKSKIQKLSKAMRDLL NT seq 642 nt NT seq  +upstreamnt  +downstreamnt atggccgcaccagcaacatccgtgctgtcccgacaggtgcggagtttcagcacatctgtg gtcaggcccttttcgaagcttgtaaggccccctgtccaggtctacggcatcgaaggccgc tatgcaaccgccctgtactctgctgcgtctaagcagaaaaggctggaccaggtggaaaag gagttgctgcgagtggggcaactcttgaaggaccccaaggtgtcccttgctgttctgaac ccctacattaagcgctccatcaaagtgaaaagcctgaaggacatcactacaaaggaaaaa ttctctccgctgacggccaacctcatgaatttacttgctgaaaatggtcgcctaggcaac acccagggcgtcatctctgccttctccaccatcatgagtgtccaccgtggagaagtgccg tgcacagtgaccacagcgtttcctttagatgaagctgttctctctgagttaaagacagtg ctgaatagcttcctgagtaaaggccagatactgaacctggaggtcaagactgacccatca atcatgggtgggatgattgtccgaattggagagaaatacgttgatatgtctgcaaagagc aagattcagaagctcagcaaggccatgcgggatctgctctga

Rattus norvegicus (rat): 245958 Help Entry 245958            CDS       T01003                                  Symbol Atp5f1e Name (RefSeq) ATP synthase subunit epsilon, mitochondrial   KO K02135   F-type H+-transporting ATPase subunit epsilon Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     245958 (Atp5f1e)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     245958 (Atp5f1e)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     245958 (Atp5f1e)   09164 Neurodegenerative disease    05010 Alzheimer disease     245958 (Atp5f1e)    05012 Parkinson disease     245958 (Atp5f1e)    05014 Amyotrophic lateral sclerosis     245958 (Atp5f1e)    05016 Huntington disease     245958 (Atp5f1e)    05020 Prion disease     245958 (Atp5f1e)    05022 Pathways of neurodegeneration - multiple diseases     245958 (Atp5f1e)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     245958 (Atp5f1e) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_Eps Motif Other DBs NCBI-GeneID:  245958 NCBI-ProteinID:  NP_620799 RGD:  621374 Ensembl:  ENSRNOG00000049912 UniProt:  P29418 LinkDB All DBs Position 3:complement(163259072..163261974) Genome browser AA seq 51 aa AA seqDB search MVAYWRQAGLSYIRFSQICAKAVRDALKTEFKANAEKTSGTSIKTVKIKKE NT seq 156 nt NT seq  +upstreamnt  +downstreamnt atggtggcgtactggcgacaggctggactcagctacatccggttctcccagatctgtgca aaagcagtgagggatgccctgaagactgagttcaaagcgaacgctgagaagacttcgggc accagcataaaaacagtgaaaataaagaaggagtag

Rattus norvegicus (rat): 245965 Help Entry 245965            CDS       T01003                                  Symbol Atp5f1d Name (RefSeq) ATP synthase subunit delta, mitochondrial precursor   KO K02134   F-type H+-transporting ATPase subunit delta Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     245965 (Atp5f1d)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     245965 (Atp5f1d)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     245965 (Atp5f1d)   09164 Neurodegenerative disease    05010 Alzheimer disease     245965 (Atp5f1d)    05012 Parkinson disease     245965 (Atp5f1d)    05014 Amyotrophic lateral sclerosis     245965 (Atp5f1d)    05016 Huntington disease     245965 (Atp5f1d)    05020 Prion disease     245965 (Atp5f1d)    05022 Pathways of neurodegeneration - multiple diseases     245965 (Atp5f1d)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     245965 (Atp5f1d) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_DE_N Motif Other DBs NCBI-GeneID:  245965 NCBI-ProteinID:  NP_620806 RGD:  621372 Ensembl:  ENSRNOG00000014625 UniProt:  P35434 LinkDB All DBs Position 7:complement(9560604..9565919) Genome browser AA seq 168 aa AA seqDB search MLPAALLRHPGLRRLVLQARTYAQAAASPAPAAGPGQMSFTFASPTQVFFDGANVRQVDV PTLTGAFGILASHVPTLQVLRPGLVVVHAEDGTTTKYFVSSGSVTVNADSSVQLLAEEVV TLDMLDLGAARANLEKAQSELSGAADEAARAEIQIRIEANEALVKALE NT seq 507 nt NT seq  +upstreamnt  +downstreamnt atgctgcccgccgcattgcttcgtcacccaggtctgcgccgtctggtgctccaggcgcgt acgtacgcccaggccgccgcctcacctgcccccgccgctgggcctggacagatgtccttc accttcgcctccccgacgcaggtgttctttgatggtgccaatgtccggcaagtggatgtg cctacgctgactggagcctttggcatcctggcatcccatgtccccacactacaggtccta cggcctgggctggtagtggttcatgcggaagatggcaccacaactaagtattttgtgagc agcggctccgtcactgtgaatgcggactcctctgtgcaattactagctgaagaagtcgtg acactggacatgctggacctcggggcagcccgggcaaacctggagaaggcgcagtcagag ctgtcaggggcagcagatgaggcagcacgggctgagatccaaatccggatcgaggccaat gaagccctggtgaaggccctggagtag

Rattus norvegicus (rat): 26196 Help Entry 26196             CDS       T01003                                  Symbol ATP8 Name (RefSeq) ATP synthase F0 subunit 8   KO K02125   F-type H+-transporting ATPase subunit 8 Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     26196 (ATP8)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     26196 (ATP8)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     26196 (ATP8)   09164 Neurodegenerative disease    05010 Alzheimer disease     26196 (ATP8)    05012 Parkinson disease     26196 (ATP8)    05014 Amyotrophic lateral sclerosis     26196 (ATP8)    05016 Huntington disease     26196 (ATP8)    05020 Prion disease     26196 (ATP8)    05022 Pathways of neurodegeneration - multiple diseases     26196 (ATP8)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     26196 (ATP8)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:rno03029]     26196 (ATP8) Mitochondrial biogenesis [BR:rno03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial DNA-encoded proteins    F-type ATPase     26196 (ATP8) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_8 Motif Other DBs NCBI-GeneID:  26196 NCBI-ProteinID:  YP_665633 RGD:  621240 UniProt:  P11608 Q8HIC8 LinkDB All DBs Position MT:7758..7961 Genome browser AA seq 67 aa AA seqDB search MPQLDTSTWFITIISSMATLFILFQLKISSQTFPAPPSPKTMATEKTNNPWESKWTKTYL PLSLPPQ NT seq 204 nt NT seq  +upstreamnt  +downstreamnt atgccacaactagacacatccacatgatttattacaatcatctcctcaatagccacacta tttattttatttcaattaaaaatttcttcccaaacctttcctgcacctccctcccccaaa actatagccacagaaaaaacgaataacccttgagaatcaaaatgaacgaaaacctatttg cctctttcattacccccacaataa

Rattus norvegicus (rat): 26197 Help Entry 26197             CDS       T01003                                  Symbol ATP6 Name (RefSeq) ATP synthase F0 subunit 6   KO K02126   F-type H+-transporting ATPase subunit a Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     26197 (ATP6)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     26197 (ATP6)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     26197 (ATP6)   09164 Neurodegenerative disease    05010 Alzheimer disease     26197 (ATP6)    05012 Parkinson disease     26197 (ATP6)    05014 Amyotrophic lateral sclerosis     26197 (ATP6)    05016 Huntington disease     26197 (ATP6)    05020 Prion disease     26197 (ATP6)    05022 Pathways of neurodegeneration - multiple diseases     26197 (ATP6)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     26197 (ATP6)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:rno03029]     26197 (ATP6) Mitochondrial biogenesis [BR:rno03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial DNA-encoded proteins    F-type ATPase     26197 (ATP6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_A Motif Other DBs NCBI-GeneID:  26197 NCBI-ProteinID:  YP_665634 RGD:  621239 UniProt:  P05504 Q8HIC7 Structure PDB LinkDB All DBs Position MT:7919..8599 Genome browser AA seq 226 aa AA seqDB search MNENLFASFITPTMMGLPIVVTIIMFPSILFPSSERLISNRLHSFQHWLIKLIIKQMMLI HTPKGRTWALMIVSLIMFIGSTNLLGLLPHTFTPTTQLSMNLSMAIPLWAGAVILGFRHK LKNSLAHFLPQGTPISLIPMLIIIETISLFIQPMALAVRLTANITAGHLLMHLIGGATLV LMDISPPTATITFIILLLLTVLEFAVALIQAYVFTLLVSLYLHDNT NT seq 681 nt NT seq  +upstreamnt  +downstreamnt atgaacgaaaacctatttgcctctttcattacccccacaataataggtctaccaattgtt gtaaccattattatgttcccatcaattctattcccatcatcagaacgcctaatcagcaac cgactacactcatttcaacactgactaatcaaacttatcatcaaacaaataatgttaatc cacacaccaaaaggacgaacctgagccctaataattgtatccctaattatatttattggc tcaaccaaccttctagggcttcttccccatacatttacccctaccactcagctatctata aacctaagcatagccatccccctatgagcaggagccgtaattctaggcttccgacacaaa ctaaaaaattctttagcccacttcttaccgcaaggaacccccatctccctaattcccata ctaattatcatcgaaactatcagcctatttattcaaccgatagcactagcagtacgacta acagcaaacattacagcaggccatctattaatgcatctaatcggaggagctactctagta cttatagacatcagcccaccaaccgctacaattacatttattattctacttctacttaca gtacttgaatttgccgtagccttaattcaagcctatgtattcacccttctagtaagcctg tacctacatgataacacataa

Rattus norvegicus (rat): 29754 Help Entry 29754             CDS       T01003                                  Symbol Atp5mc1 Name (RefSeq) ATP synthase F(0) complex subunit C1, mitochondrial precursor   KO K02128   F-type H+-transporting ATPase subunit c Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     29754 (Atp5mc1)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     29754 (Atp5mc1)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     29754 (Atp5mc1)   09164 Neurodegenerative disease    05010 Alzheimer disease     29754 (Atp5mc1)    05012 Parkinson disease     29754 (Atp5mc1)    05014 Amyotrophic lateral sclerosis     29754 (Atp5mc1)    05016 Huntington disease     29754 (Atp5mc1)    05020 Prion disease     29754 (Atp5mc1)    05022 Pathways of neurodegeneration - multiple diseases     29754 (Atp5mc1)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     29754 (Atp5mc1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_C Motif Other DBs NCBI-GeneID:  29754 NCBI-ProteinID:  NP_059007 RGD:  61933 Ensembl:  ENSRNOG00000007235 UniProt:  Q06645 LinkDB All DBs Position 10:complement(81024056..81026780) Genome browser AA seq 136 aa AA seqDB search MQTTKALLISPVLIRSCTRGLIRPVSASLLSRPEAPSKKPSCCSSPLQVARREFQTSVIS RDIDTAAKFIGAGAATVGVAGSGAGIGTVFGSLIIGYARNPSLKQQLFSYAILGFALSEA MGLFCLMVAFLILFAM NT seq 411 nt NT seq  +upstreamnt  +downstreamnt atgcagaccacgaaggcactgctcatttctccagttctgatccgctcctgtaccaggggt ctaatcaggcctgtgtctgcctccctcctgagtagaccagaggctccatctaaaaagcct tcctgctgcagctcccctctccaggtggccagacgggaattccagaccagtgttatttcc cgggacattgacacagcagccaagtttattggtgctggggccgccacagttggtgtggct ggatcaggggctggcattggcacagtgtttggtagcttgattattggctatgccaggaac ccgtctctcaagcagcagctcttctcctatgccatcctgggctttgccctgtctgaggcc atggggctcttctgtttgatggtcgccttcctcatcctcttcgccatgtga

Rattus norvegicus (rat): 641434 Help Entry 641434            CDS       T01003                                  Symbol Atp5pd Name (RefSeq) ATP synthase subunit d, mitochondrial   KO K02138   F-type H+-transporting ATPase subunit d Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     641434 (Atp5pd)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     641434 (Atp5pd)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     641434 (Atp5pd)   09164 Neurodegenerative disease    05010 Alzheimer disease     641434 (Atp5pd)    05012 Parkinson disease     641434 (Atp5pd)    05014 Amyotrophic lateral sclerosis     641434 (Atp5pd)    05016 Huntington disease     641434 (Atp5pd)    05020 Prion disease     641434 (Atp5pd)    05022 Pathways of neurodegeneration - multiple diseases     641434 (Atp5pd)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     641434 (Atp5pd) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mt_ATP-synt_D RE_Eco47II Motif Other DBs NCBI-GeneID:  641434 NCBI-ProteinID:  NP_062256 RGD:  620083 Ensembl:  ENSRNOG00000003626 UniProt:  P31399 LinkDB All DBs Position 10:complement(100657700..100662960) Genome browser AA seq 161 aa AA seqDB search MAGRKLALKTIDWVSFVEIMPQNQKAIGNALKSWNETFHTRLASLSEKPPAIDWAYYRAN VDKPGLVDDFKNKYNALKIPVPEDKYTALVDAEEKEDVKNCAQFVTGSQARVREYEKQLE KIKNMIPFDQMTIDDLNEVFPETKLDKRKYPYWPHQPIENL NT seq 486 nt NT seq  +upstreamnt  +downstreamnt atggctgggcgcaaacttgctctaaaaaccatcgattgggtatcttttgtggagatcatg ccccaaaaccagaaggcaattggaaacgctctgaagtcctggaatgagaccttccacacc aggttggctagtctgtctgagaaaccaccagcgattgactgggcttactacagggccaat gtggacaagcctggcttggtggatgattttaaaaacaagtataatgctctgaagatccct gtgcctgaggataaatacacagccctagtggacgccgaggagaaggaggatgtgaagaac tgtgcccagttcgtgactggatctcaggctagggtccgggaatatgagaagcagctggag aaaataaagaacatgattccctttgaccagatgacgattgatgacttgaatgaggtcttc cctgaaaccaagctggacaagaggaagtacccatactggccccatcagcccatcgagaac ctgtga

Rattus norvegicus (rat): 65262 Help Entry 65262             CDS       T01003                                  Symbol Atp5f1a Name (RefSeq) ATP synthase subunit alpha, mitochondrial precursor   KO K02132   F-type H+-transporting ATPase subunit alpha Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     65262 (Atp5f1a)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     65262 (Atp5f1a)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     65262 (Atp5f1a)   09164 Neurodegenerative disease    05010 Alzheimer disease     65262 (Atp5f1a)    05012 Parkinson disease     65262 (Atp5f1a)    05014 Amyotrophic lateral sclerosis     65262 (Atp5f1a)    05016 Huntington disease     65262 (Atp5f1a)    05020 Prion disease     65262 (Atp5f1a)    05022 Pathways of neurodegeneration - multiple diseases     65262 (Atp5f1a)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     65262 (Atp5f1a) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_ab ATP-synt_ab_C ATP-synt_ab_N DUF4142 Motif Other DBs NCBI-GeneID:  65262 NCBI-ProteinID:  NP_075581 RGD:  619993 Ensembl:  ENSRNOG00000017032 UniProt:  P15999 Structure PDB LinkDB All DBs Position 18:71292406..71300342 Genome browser AA seq 553 aa AA seqDB search MLSVRIAAAVARALPRRAGLVSKNALGSSFVGTRNLHASNTRLQKTGTAEMSSILEERIL GADTSVDLEETGRVLSIGDGIARVHGLRNVQAEEMVEFSSGLKGMSLNLEPDNVGVVVFG NDKLIKEGDIVKRTGAIVDVPVGDELLGRVVDALGNAIDGKGPVGSKIRRRVGLKAPGII PRISVREPMQTGIKAVDSLVPIGRGQRELIIGDRQTGKTSIAIDTIINQKRFNDGTDEKK KLYCIYVAIGQKRSTVAQLVKRLTDADAMKYTIVVSATASDAAPLQYLAPYSGCSMGEYF RDNGKHALIIYDDLSKQAVAYRQMSLLLRRPPGREAYPGDVFYLHSRLLERAAKMNDSFG GGSLTALPVIETQAGDVSAYIPTNVISITDGQIFLETELFYKGIRPAINVGLSVSRVGSA AQTRAMKQVAGTMKLELAQYREVAAFAQFGSDLDAATQQLLSRGVRLTELLKQGQYSPMA IEEQVAVIYAGVRGYLDKLEPSKITKFESAFLSHVVSQHQSLLGNIRSDGKISEQSDAKL KEIVTNFLAGFEP NT seq 1662 nt NT seq  +upstreamnt  +downstreamnt atgctgtccgtgcgcatcgccgcggccgtggcccgtgccctccctcgacgggcgggactg gtctccaaaaatgccttggggtcatcttttgttggtacaagaaatctccatgcctctaac actcgacttcagaagactggcactgccgagatgtcctccattctcgaggagcggatcctt ggagctgatacttctgttgaccttgaagagactggccgtgtcttaagcattggtgatggt attgcccgagtgcatggactgaggaacgttcaagctgaggagatggtagagttttcttcc ggcttaaagggtatgtccctgaacttggaacccgacaatgttggagttgtcgtgtttggg aatgacaagctaattaaagaaggtgatatcgtgaagagaacaggagccatcgtggacgtt ccagttggcgatgaactgttgggccgtgtagttgatgccctgggaaatgccattgatggg aagggtccagttggttccaagattcgcagacgagtgggcctgaaagcccctggaattatc ccccgaatctctgtgcgggaaccaatgcagacgggcatcaaggctgtggatagcctggtg ccgattggccgaggtcagcgtgagctgattattggagacagacagaccgggaaaacctcg attgctattgacacaatcatcaaccagaagcgtttcaatgatgggactgacgagaagaag aaactgtactgcatctacgttgctattggtcagaaacggtccaccgttgctcagttggtg aagagactgacagacgcagatgccatgaagtacaccattgtggtgtcagccactgcctct gatgctgccccgcttcagtacttggctccttactccggctgctccatgggagagtatttc cgagataatggcaagcacgctctgatcatctatgacgacttatccaagcaggctgttgct taccgccagatgtctctgctgctccgccgacccccgggtcgagaggcctatcccggtgat gtgttttacctacactctcgcctgctggagagagcagccaagatgaacgattcctttggt ggtggctctttgactgccttaccagtcattgaaacacaggctggtgatgtgtccgcctac attccaacaaacgttatttccatcaccgatggacagatcttcttggaaacagaattgttc tataaaggcatccgccctgccattaatgtgggcttgtctgtgtcccgtgtcggatctgcc gcccagaccagagccatgaagcaggtggcaggcaccatgaagctggagttggcccagtac cgggaggtcgctgcttttgcccagtttggttctgatctggatgctgccactcagcagctc ttgagccgtggcgtgcgcctgaccgagctgctaaagcaaggacagtactctcccatggct attgaagaacaggtggctgtcatctatgcaggcgtccggggttatcttgataaactggag cccagtaagatcacaaagttcgagagtgctttcttgtctcatgttgtgagccagcaccag agcctcttgggcaatatcaggtctgatgggaaaatctcagaacagtcggatgcaaagctg aaggaaatcgtaacaaacttcttggctgggtttgaaccttaa

Rattus norvegicus (rat): 94271 Help Entry 94271             CDS       T01003                                  Symbol Atp5pf Name (RefSeq) ATP synthase-coupling factor 6, mitochondrial precursor   KO K02131   F-type H+-transporting ATPase subunit 6 Organism rno  Rattus norvegicus (rat) Pathway rno00190   Oxidative phosphorylation rno01100   Metabolic pathways rno04714   Thermogenesis rno05010   Alzheimer disease rno05012   Parkinson disease rno05014   Amyotrophic lateral sclerosis rno05016   Huntington disease rno05020   Prion disease rno05022   Pathways of neurodegeneration - multiple diseases rno05208   Chemical carcinogenesis - reactive oxygen species rno05415   Diabetic cardiomyopathy Module rno_M00158   F-type ATPase, eukaryotes Brite KEGG Orthology (KO) [BR:rno00001]  09100 Metabolism   09102 Energy metabolism    00190 Oxidative phosphorylation     94271 (Atp5pf)  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     94271 (Atp5pf)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     94271 (Atp5pf)   09164 Neurodegenerative disease    05010 Alzheimer disease     94271 (Atp5pf)    05012 Parkinson disease     94271 (Atp5pf)    05014 Amyotrophic lateral sclerosis     94271 (Atp5pf)    05016 Huntington disease     94271 (Atp5pf)    05020 Prion disease     94271 (Atp5pf)    05022 Pathways of neurodegeneration - multiple diseases     94271 (Atp5pf)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     94271 (Atp5pf) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ATP-synt_F6 RICH Motif Other DBs NCBI-GeneID:  94271 NCBI-ProteinID:  NP_446054 RGD:  621376 Ensembl:  ENSRNOG00000001551 UniProt:  P21571 LinkDB All DBs Position 11:complement(23881594..23889581) Genome browser AA seq 108 aa AA seqDB search MTVQRIFRLSSVLRSAVSVHLRRNIGVTAVAFNKELDPVQKLFLDKIREYKAKRLASGGP VDTGPEYQQEVDRELFKLKQMYGKGEMDKFPTFNFEDPKFEVLDKPQS NT seq 327 nt NT seq  +upstreamnt  +downstreamnt atgactgttcagaggatcttcaggctctcctctgtccttcggtcagcagtctctgtgcat ttgaggaggaacattggtgttacagctgtggcgtttaataaggaacttgatcctgtacag aaactcttcttggacaagataagagagtacaaagcaaagcgactggcgtctggaggacct gttgatactggcccagaatatcagcaagaggtggacagagagctttttaagcttaaacaa atgtatggtaaaggagagatggataagtttcctaccttcaattttgaggatcccaaattt gaagtcctcgacaaaccccagtcctga

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