Camelus dromedarius (Arabian camel): 105087057 Help Entry 105087057         CDS       T04642                                  Symbol SLC25A31 Name (RefSeq) ADP/ATP translocase 4   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism cdk  Camelus dromedarius (Arabian camel) Pathway cdk04020   Calcium signaling pathway cdk04022   cGMP-PKG signaling pathway cdk04217   Necroptosis cdk04218   Cellular senescence cdk04613   Neutrophil extracellular trap formation cdk05010   Alzheimer disease cdk05012   Parkinson disease cdk05016   Huntington disease cdk05017   Spinocerebellar ataxia cdk05020   Prion disease cdk05022   Pathways of neurodegeneration - multiple diseases cdk05164   Influenza A cdk05166   Human T-cell leukemia virus 1 infection cdk05208   Chemical carcinogenesis - reactive oxygen species cdk05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:cdk00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     105087057 (SLC25A31)    04022 cGMP-PKG signaling pathway     105087057 (SLC25A31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     105087057 (SLC25A31)    04218 Cellular senescence     105087057 (SLC25A31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     105087057 (SLC25A31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     105087057 (SLC25A31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     105087057 (SLC25A31)    05164 Influenza A     105087057 (SLC25A31)   09164 Neurodegenerative disease    05010 Alzheimer disease     105087057 (SLC25A31)    05012 Parkinson disease     105087057 (SLC25A31)    05016 Huntington disease     105087057 (SLC25A31)    05017 Spinocerebellar ataxia     105087057 (SLC25A31)    05020 Prion disease     105087057 (SLC25A31)    05022 Pathways of neurodegeneration - multiple diseases     105087057 (SLC25A31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     105087057 (SLC25A31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:cdk03029]     105087057 (SLC25A31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:cdk02000]     105087057 (SLC25A31) Mitochondrial biogenesis [BR:cdk03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     105087057 (SLC25A31) Transporters [BR:cdk02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    105087057 (SLC25A31) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  105087057 NCBI-ProteinID:  XP_010975965 LinkDB All DBs Position 2:complement(31250081..31273685) Genome browser AA seq 323 aa AA seqDB search MQRDLQKKKQEKKAEKRLFDAGSFGKDLLAGGVAAAVSKTTVAPIERVKLLLQVQASSKQ ISPEAQYKGMIDCLVRIPREQGFLSYWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVN KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIMKI AKSDGIVGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLVSFFIAQVVTTCS GILSYPFDTVRRRMMMQSGEAERQYKGTLDCFVKIYQHEGVSAFFRGAFSNILRGTGGAL VLVLYDKIKEFLNIDIRGSSSGD NT seq 972 nt NT seq  +upstreamnt  +downstreamnt atgcagcgtgatcttcagaagaagaagcaggagaagaaggcggaaaagcggctctttgac gccgggtccttcgggaaggacctgctggcaggcggggtggcggcggctgtgtccaagacg acggtggcgcccatcgagcgggtgaagctgctgctgcaggtgcaggcgtcgtccaagcag atcagccccgaggcgcagtacaaaggcatgatcgactgcctggtgcggattcctcgtgag caaggtttcctcagttattggcgtggcaacttggcaaatgtcatccggtattttccaaca caagctctaaactttgcttttaaagacaaatacaaacaacttttcatgtccggagttaat aaagaaaaacagttctggaggtggtttttggcaaacctggcttctggtggagctgctggg gcaacatccttatgtgtagtatatccgctagattttgctcgaacccgattaggtgttgat attggaaaaggtcctgaagagcgacaattcaagggtttaggtgactgtattatgaaaata gcaaaatcagatggaattgttggtctataccaagggtttggtgtttcagttcagggcatc attgtgtacagagcctcttattttggagcttatgacacagttaagggcttattaccaaaa ccaaaggaaactccatttcttgtctcctttttcattgctcaagttgtgactacatgctcc ggaatactctcttatccctttgatacagttagaagacgtatgatgatgcagagtggtgag gctgaacggcaatataaaggaactttagactgctttgtgaagatataccaacatgaagga gtcagtgcattttttcgtggtgccttctccaatatccttcgtggtacagggggtgctttg gtgttggtattatatgataaaattaaagaattccttaatattgatattagaggtagttca tcaggagattaa

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