Oryctolagus cuniculus (rabbit): 100009414 Help Entry 100009414         CDS       T03373                                  Symbol SLC25A4, SLC25A5 Name (RefSeq) solute carrier family 25 member 4   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04020   Calcium signaling pathway ocu04022   cGMP-PKG signaling pathway ocu04217   Necroptosis ocu04218   Cellular senescence ocu04613   Neutrophil extracellular trap formation ocu05010   Alzheimer disease ocu05012   Parkinson disease ocu05016   Huntington disease ocu05017   Spinocerebellar ataxia ocu05020   Prion disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05164   Influenza A ocu05166   Human T-cell leukemia virus 1 infection ocu05208   Chemical carcinogenesis - reactive oxygen species ocu05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     100009414 (SLC25A4)    04022 cGMP-PKG signaling pathway     100009414 (SLC25A4)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     100009414 (SLC25A4)    04218 Cellular senescence     100009414 (SLC25A4)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     100009414 (SLC25A4)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     100009414 (SLC25A4)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     100009414 (SLC25A4)    05164 Influenza A     100009414 (SLC25A4)   09164 Neurodegenerative disease    05010 Alzheimer disease     100009414 (SLC25A4)    05012 Parkinson disease     100009414 (SLC25A4)    05016 Huntington disease     100009414 (SLC25A4)    05017 Spinocerebellar ataxia     100009414 (SLC25A4)    05020 Prion disease     100009414 (SLC25A4)    05022 Pathways of neurodegeneration - multiple diseases     100009414 (SLC25A4)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     100009414 (SLC25A4)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:ocu03029]     100009414 (SLC25A4)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:ocu02000]     100009414 (SLC25A4) Mitochondrial biogenesis [BR:ocu03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     100009414 (SLC25A4) Transporters [BR:ocu02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    100009414 (SLC25A4) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  100009414 NCBI-ProteinID:  NP_001076155 Ensembl:  ENSOCUG00000002594 UniProt:  O46373 LinkDB All DBs Position 2:62604009..62607533 Genome browser AA seq 298 aa AA seqDB search MSDQALSFLKDFLAGGVAAAVSKTAVAPIERVKLLLQVQHASKQISAEKQYKGIIDCVVR IPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDRHKQFWRYFAGNLASG GAAGATSLCFVYPLDFARTRLAADVGKGAAQREFSGLGNCLTKIFKSDGLRGLYQGFNVS VQGIIIYRAAYFGVYDTAKGMLPDPKNVHIIVSWMIAQTVTAVAGLVSYPFDTVRRRMMM QSGRKGADIMYTGTVDCWKKIAKDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYV NT seq 897 nt NT seq  +upstreamnt  +downstreamnt atgagtgatcaggctttgagcttcctcaaggacttcctggcaggtggcgtcgccgctgcc gtctccaagactgcggtcgcccccatcgagagggtcaaactgctgctgcaggtccagcat gccagcaaacagatcagcgctgagaagcagtacaaagggatcattgattgtgtggtgagg atccccaaggagcagggctttctctccttctggaggggtaacctggccaacgtgatccgg tacttccccacccaagctctcaacttcgccttcaaggacaagtacaagcagatcttcttg gggggcgtggatcggcataagcagttctggcgctacttcgctggtaacctggcctccggt ggggcagctggggccacctccctctgctttgtctacccgctggactttgccaggaccagg ttggctgccgacgtgggcaagggtgccgcccagcgtgagttcagtggtctgggcaactgt ctcaccaagatcttcaagtctgatggcctgaggggtctctaccagggtttcaatgtctct gtgcaaggcatcattatctacagagctgcctacttcggagtctatgatactgccaagggg atgttgcctgaccccaagaacgtgcacattatcgtgagctggatgatcgcccagaccgtg acggcagtggccgggctggtgtcctacccctttgacactgttcgtcgtaggatgatgatg cagtctggccggaaaggggctgacattatgtacacggggacagttgactgctggaagaag attgcaaaagatgaaggagccaaggctttcttcaaaggtgcctggtccaatgtgttgaga ggcatgggtggcgcttttgtattggtgttgtatgatgagatcaaaaaatatgtctaa

Oryctolagus cuniculus (rabbit): 100337764 Help Entry 100337764         CDS       T03373                                  Symbol SLC25A5 Name (RefSeq) solute carrier family 25 member 5   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04020   Calcium signaling pathway ocu04022   cGMP-PKG signaling pathway ocu04217   Necroptosis ocu04218   Cellular senescence ocu04613   Neutrophil extracellular trap formation ocu05010   Alzheimer disease ocu05012   Parkinson disease ocu05016   Huntington disease ocu05017   Spinocerebellar ataxia ocu05020   Prion disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05164   Influenza A ocu05166   Human T-cell leukemia virus 1 infection ocu05208   Chemical carcinogenesis - reactive oxygen species ocu05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     100337764 (SLC25A5)    04022 cGMP-PKG signaling pathway     100337764 (SLC25A5)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     100337764 (SLC25A5)    04218 Cellular senescence     100337764 (SLC25A5)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     100337764 (SLC25A5)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     100337764 (SLC25A5)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     100337764 (SLC25A5)    05164 Influenza A     100337764 (SLC25A5)   09164 Neurodegenerative disease    05010 Alzheimer disease     100337764 (SLC25A5)    05012 Parkinson disease     100337764 (SLC25A5)    05016 Huntington disease     100337764 (SLC25A5)    05017 Spinocerebellar ataxia     100337764 (SLC25A5)    05020 Prion disease     100337764 (SLC25A5)    05022 Pathways of neurodegeneration - multiple diseases     100337764 (SLC25A5)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     100337764 (SLC25A5)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:ocu03029]     100337764 (SLC25A5)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:ocu02000]     100337764 (SLC25A5) Mitochondrial biogenesis [BR:ocu03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     100337764 (SLC25A5) Transporters [BR:ocu02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    100337764 (SLC25A5) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  100337764 NCBI-ProteinID:  XP_002720308 Ensembl:  ENSOCUG00000013268 UniProt:  G1T524 LinkDB All DBs Position X:68185693..68188505 Genome browser AA seq 298 aa AA seqDB search MTDAAVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFRGLGDCLVKIYKSDGIRGLYQGFNVS VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM QSGRKGTDIMYTGTLDCWRKIARDEGGKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT NT seq 897 nt NT seq  +upstreamnt  +downstreamnt atgacagatgccgctgtgtccttcgccaaggactttctggcaggtggagtggctgcggcc atctccaagaccgcggtagcgcccatcgagagggtcaagctgctgctgcaggtgcagcat gccagcaagcaaatcactgccgataagcaatacaagggcattatagactgcgtggttcgt atccccaaggagcagggagtcctgtccttctggcgtggtaacctggccaatgtcatcaga tacttccccacccaggctctcaactttgccttcaaagataaatacaagcagatctttctg ggtggcgtggacaagaggacccagttttggcgctactttgcaggaaatctggcatcaggt ggtgctgctggagccacatccttgtgtttcgtgtaccctcttgattttgcccgtacccgt ctagcagctgacgtgggcaaagctggagctgaaagggaattcagaggcctcggcgactgc ctggttaagatctacaaatctgatgggattaggggcctgtaccaaggctttaatgtgtct gtacagggcattatcatctaccgggctgcctacttcggtatctatgacaccgcaaaagga atgcttccagatcccaagaacacacacatcttcatcagctggatgattgcgcagtctgtc actgctgttgctgggttgacttcctatccatttgacactgttcgtcggcgcatgatgatg cagtcggggcgtaaaggaactgatatcatgtacacaggcacacttgactgctggaggaag attgctcgtgatgaaggaggcaaagcgtttttcaagggtgcatggtccaacgtcctcaga ggcatgggtggtgcttttgtgcttgtcttgtatgatgaaatcaagaagttcacataa

Oryctolagus cuniculus (rabbit): 100346477 Help Entry 100346477         CDS       T03373                                  Symbol SLC25A31 Name (RefSeq) solute carrier family 25 member 31   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04020   Calcium signaling pathway ocu04022   cGMP-PKG signaling pathway ocu04217   Necroptosis ocu04218   Cellular senescence ocu04613   Neutrophil extracellular trap formation ocu05010   Alzheimer disease ocu05012   Parkinson disease ocu05016   Huntington disease ocu05017   Spinocerebellar ataxia ocu05020   Prion disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05164   Influenza A ocu05166   Human T-cell leukemia virus 1 infection ocu05208   Chemical carcinogenesis - reactive oxygen species ocu05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     100346477 (SLC25A31)    04022 cGMP-PKG signaling pathway     100346477 (SLC25A31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     100346477 (SLC25A31)    04218 Cellular senescence     100346477 (SLC25A31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     100346477 (SLC25A31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     100346477 (SLC25A31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     100346477 (SLC25A31)    05164 Influenza A     100346477 (SLC25A31)   09164 Neurodegenerative disease    05010 Alzheimer disease     100346477 (SLC25A31)    05012 Parkinson disease     100346477 (SLC25A31)    05016 Huntington disease     100346477 (SLC25A31)    05017 Spinocerebellar ataxia     100346477 (SLC25A31)    05020 Prion disease     100346477 (SLC25A31)    05022 Pathways of neurodegeneration - multiple diseases     100346477 (SLC25A31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     100346477 (SLC25A31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:ocu03029]     100346477 (SLC25A31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:ocu02000]     100346477 (SLC25A31) Mitochondrial biogenesis [BR:ocu03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     100346477 (SLC25A31) Transporters [BR:ocu02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    100346477 (SLC25A31) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  100346477 NCBI-ProteinID:  XP_002717308 Ensembl:  ENSOCUG00000015617 LinkDB All DBs Position 15:103560352..103588642 Genome browser AA seq 322 aa AA seqDB search MQREPAKKKPEKKAEKRLFDAASFGRDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQ ISPETRYKGMVDCLVRIPREQGFFSYWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVN KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIMKI AKSDGIVGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLISFFIAQVVTTCS GILSYPFDTVRRRMMMQSGEAERQYKGTLDCFVKIYQHEGINAFFRGAFSNILRGTGGAL VLVLYDKIKEFLKIDIGGGSSD NT seq 969 nt NT seq  +upstreamnt  +downstreamnt atgcagcgtgagcctgccaagaagaagccggagaagaaggctgagaagcggctgtttgac gccgcatccttcggaagggacctgctggccggcggggtcgcggcggctgtgtccaagacg gcagtggcgcccatcgagcgggtgaagctcctcctgcaggtgcaggcgtcgtccaagcag atcagccccgagacgcgctacaagggcatggtggactgcctggtgcggattccccgcgag cagggtttctttagttattggcgaggcaatttggcaaatgttatccggtactttccaaca caagctctaaattttgcttttaaagacaaatacaaacaacttttcatgtctggagttaat aaagaaaaacagttctggaggtggtttttggcaaacctggcttctggtggagctgccgga gcaacatctttgtgtgtggtttatcctctagattttgcccgaactcggttaggtgttgac attggaaaaggtcctgaagagcgacaattcaagggtctaggtgactgcattatgaaaata gcaaaatcagatggcatagttggtttataccaagggtttggtgtttcagttcagggaatc attgtgtaccgagcctcttactttggagcttatgacacagttaagggcttattaccaaaa ccaaaagaaactccatttcttatctcctttttcattgctcaagttgtgactacatgctct ggaatactctcttacccctttgatacagtgagaagacgcatgatgatgcagagtggtgaa gctgaacggcagtataaaggaaccttagactgctttgtgaagatataccaacatgaggga atcaatgcattttttcgtggtgccttctccaatatccttcgtggtacagggggtgctttg gtgttggtgttatatgataaaattaaagaattccttaaaattgatattggaggtggttca tcagattaa

Oryctolagus cuniculus (rabbit): 100349768 Help Entry 100349768         CDS       T03373                                  Name (RefSeq) ADP/ATP translocase 1   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04020   Calcium signaling pathway ocu04022   cGMP-PKG signaling pathway ocu04217   Necroptosis ocu04218   Cellular senescence ocu04613   Neutrophil extracellular trap formation ocu05010   Alzheimer disease ocu05012   Parkinson disease ocu05016   Huntington disease ocu05017   Spinocerebellar ataxia ocu05020   Prion disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05164   Influenza A ocu05166   Human T-cell leukemia virus 1 infection ocu05208   Chemical carcinogenesis - reactive oxygen species ocu05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     100349768    04022 cGMP-PKG signaling pathway     100349768  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     100349768    04218 Cellular senescence     100349768  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     100349768  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     100349768   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     100349768    05164 Influenza A     100349768   09164 Neurodegenerative disease    05010 Alzheimer disease     100349768    05012 Parkinson disease     100349768    05016 Huntington disease     100349768    05017 Spinocerebellar ataxia     100349768    05020 Prion disease     100349768    05022 Pathways of neurodegeneration - multiple diseases     100349768   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     100349768  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:ocu03029]     100349768   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:ocu02000]     100349768 Mitochondrial biogenesis [BR:ocu03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     100349768 Transporters [BR:ocu02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    100349768 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  100349768 NCBI-ProteinID:  XP_002715967 Ensembl:  ENSOCUG00000024057 UniProt:  O46373 LinkDB All DBs Position 13:complement(91740807..91742138) Genome browser AA seq 298 aa AA seqDB search MSDQALSFLKDFLAGGVAAAVSKTAVAPIERVKLLLQVQHASKQISAEKQYKGIIDCVVR IPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDRHKQFWRYFAGNLASG GAAGATSLCFVYPLDFARTRLAADVGKGAAQREFSGLGNCLTKIFKSDGLRGLYQGFNVS VQGIIIYRAAYFGVYDTAKGMLPDPKNVHIIVSWMIAQTVTAVAGLVSYPFDTVRRRMMM QSGRKGADIMYTGTVDCWKKIAKDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYV NT seq 897 nt NT seq  +upstreamnt  +downstreamnt atgagtgatcaggctttgagcttcctcaaggacttcctggcaggtggcgtcgccgctgcc gtctccaagactgcggtcgcccccatcgagagggtcaaactgctgctgcaggtccagcat gccagcaaacagatcagcgctgagaagcagtacaaagggatcattgattgtgtggtgagg atccccaaggagcagggctttctctccttctggaggggtaacctggccaacgtgatccgg tacttccccacccaagctctcaacttcgccttcaaggacaagtacaagcagatcttcttg gggggcgtggatcggcataagcagttctggcgctacttcgctggtaacctggcctccggt ggggcagctggggccacctccctctgctttgtctacccgctggactttgccaggaccagg ttggctgccgacgtgggcaagggtgccgcccagcgtgagttcagtggtctgggcaactgt ctcaccaagatcttcaagtctgatggcctgaggggtctctaccagggtttcaatgtctct gtgcaaggcatcattatctacagagctgcctacttcggagtctatgatactgccaagggg atgttgcctgaccccaagaacgtgcacattatcgtgagctggatgatcgcccagactgtg acggcagtggccgggctggtgtcctacccctttgacactgttcgtcgtaggatgatgatg cagtctggccggaaaggggctgacattatgtacacggggacagttgactgctggaagaag attgcaaaagatgaaggagccaaggctttcttcaaaggtgcctggtccaatgtgttgaga ggcatgggtggcgcttttgtattggtgttgtatgatgagatcaaaaaatatgtctaa

Oryctolagus cuniculus (rabbit): 100356326 Help Entry 100356326         CDS       T03373                                  Name (RefSeq) ADP/ATP translocase 2   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism ocu  Oryctolagus cuniculus (rabbit) Pathway ocu04020   Calcium signaling pathway ocu04022   cGMP-PKG signaling pathway ocu04217   Necroptosis ocu04218   Cellular senescence ocu04613   Neutrophil extracellular trap formation ocu05010   Alzheimer disease ocu05012   Parkinson disease ocu05016   Huntington disease ocu05017   Spinocerebellar ataxia ocu05020   Prion disease ocu05022   Pathways of neurodegeneration - multiple diseases ocu05164   Influenza A ocu05166   Human T-cell leukemia virus 1 infection ocu05208   Chemical carcinogenesis - reactive oxygen species ocu05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:ocu00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     100356326    04022 cGMP-PKG signaling pathway     100356326  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     100356326    04218 Cellular senescence     100356326  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     100356326  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     100356326   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     100356326    05164 Influenza A     100356326   09164 Neurodegenerative disease    05010 Alzheimer disease     100356326    05012 Parkinson disease     100356326    05016 Huntington disease     100356326    05017 Spinocerebellar ataxia     100356326    05020 Prion disease     100356326    05022 Pathways of neurodegeneration - multiple diseases     100356326   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     100356326  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:ocu03029]     100356326   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:ocu02000]     100356326 Mitochondrial biogenesis [BR:ocu03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     100356326 Transporters [BR:ocu02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    100356326 BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  100356326 NCBI-ProteinID:  XP_002720265 UniProt:  G1T524 LinkDB All DBs Position X:61082200..61083410 Genome browser AA seq 298 aa AA seqDB search MTDAAVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFRGLGDCLVKIYKSDGIRGLYQGFNVS VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM QSGRKGTDIMYTGTLDCWRKIARDEGGKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT NT seq 897 nt NT seq  +upstreamnt  +downstreamnt atgacagatgccgctgtgtccttcgccaaggactttctggcaggtggagtggctgcggcc atctccaagaccgcggtagcgcccatcgagagggtcaagctgctgctgcaggtgcagcat gccagcaagcaaatcactgccgataagcaatacaagggcattatagactgcgtggttcgt atccccaaggagcagggagtcctgtccttctggcgtggtaacctggccaatgtcatcaga tacttccccacccaggctctcaactttgccttcaaagataaatacaagcagatctttctg ggtggcgtggacaagaggacccagttttggcgctactttgcaggaaatctggcatcaggt ggtgctgctggagccacatccttgtgttttgtgtaccctcttgattttgcccgtacccgt ctagcagctgacgtgggcaaagctggagctgaaagggaattcagaggcctcggcgactgc ctggttaagatctacaaatctgatgggattaggggcctgtaccaaggctttaatgtgtct gtacagggcattatcatctaccgggctgcctacttcggtatctatgacaccgcaaaagga atgcttccagatcccaagaacacgcacatcttcatcagctggatgatcgcgcagtctgtc actgctgttgctgggttgacttcctatccatttgacactgttcgtcggcgcatgatgatg cagtccgggcgtaaaggaactgatatcatgtacacaggcacacttgactgctggaggaag attgctcgtgatgaaggaggcaaagcgtttttcaagggtgcatggtctaacgtcctcaga ggcatgggtggtgcttttgtgcttgtcttgtatgatgaaatcaagaagttcacataa

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