Mustela putorius furo (domestic ferret): 101689099 Help Entry 101689099         CDS       T07239                                  Symbol SLC25A31 Name (RefSeq) ADP/ATP translocase 4   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism mpuf  Mustela putorius furo (domestic ferret) Pathway mpuf04020   Calcium signaling pathway mpuf04022   cGMP-PKG signaling pathway mpuf04217   Necroptosis mpuf04218   Cellular senescence mpuf04613   Neutrophil extracellular trap formation mpuf05010   Alzheimer disease mpuf05012   Parkinson disease mpuf05016   Huntington disease mpuf05017   Spinocerebellar ataxia mpuf05020   Prion disease mpuf05022   Pathways of neurodegeneration - multiple diseases mpuf05164   Influenza A mpuf05166   Human T-cell leukemia virus 1 infection mpuf05208   Chemical carcinogenesis - reactive oxygen species mpuf05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:mpuf00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     101689099 (SLC25A31)    04022 cGMP-PKG signaling pathway     101689099 (SLC25A31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     101689099 (SLC25A31)    04218 Cellular senescence     101689099 (SLC25A31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     101689099 (SLC25A31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101689099 (SLC25A31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     101689099 (SLC25A31)    05164 Influenza A     101689099 (SLC25A31)   09164 Neurodegenerative disease    05010 Alzheimer disease     101689099 (SLC25A31)    05012 Parkinson disease     101689099 (SLC25A31)    05016 Huntington disease     101689099 (SLC25A31)    05017 Spinocerebellar ataxia     101689099 (SLC25A31)    05020 Prion disease     101689099 (SLC25A31)    05022 Pathways of neurodegeneration - multiple diseases     101689099 (SLC25A31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101689099 (SLC25A31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:mpuf03029]     101689099 (SLC25A31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:mpuf02000]     101689099 (SLC25A31) Mitochondrial biogenesis [BR:mpuf03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     101689099 (SLC25A31) Transporters [BR:mpuf02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    101689099 (SLC25A31) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  101689099 NCBI-ProteinID:  XP_004747994 Ensembl:  ENSMPUG00000017378 UniProt:  M3Z106 LinkDB All DBs Position Unknown AA seq 323 aa AA seqDB search MQREPPKTKQEKKSEKRLFDPASFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQ ISAETQYKGMVDCLVRIPREQGFFSFWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVN KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGADIGKGPEERQFKGLGDCIIKI AKSDGIVGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLVSFFIAQVVTTCS GILSYPFDTVRRRMMMQSGEVERQYKGTLDCFVKIYQHEGISAFFRGAFSNILRGTGGAL VLVLYDKIKEFLNIDIGGSSSGD NT seq 972 nt NT seq  +upstreamnt  +downstreamnt atgcagcgtgaacctccgaagacgaagcaagagaagaagtcggaaaagcggctctttgac cccgcgtccttcgggaaggacctgctggcaggcggggtcgcagcggctgtgtccaagacc gcggtggcccccatcgagcgggtgaagctgctgctgcaggtgcaggcgtcttccaagcag atcagtgccgagacgcagtacaaaggcatggtggactgcctggtgcggattccccgagag caaggtttcttcagtttttggcgtggcaatttggccaatgttatccgatattttccaaca caagctcttaactttgcgtttaaggacaaatacaaacaacttttcatgtctggagttaat aaagaaaagcagttctggaggtggtttttggcaaacctggcttctggtggagctgctgga gcaacatccttatgtgtagtttatccgctagactttgcccgaacccgattaggtgctgat attggaaaaggtcctgaagagcgacaattcaagggtttaggtgactgtattataaaaata gcaaaatcagacggaattgttggtttgtaccaagggtttggtgtttcagttcagggtatc attgtgtaccgagcctcctattttggagcatatgacacagttaagggcttattaccaaaa ccaaaggaaaccccatttcttgtctcctttttcattgctcaagttgtgaccacatgctct ggaattctttcttatccctttgacacagttagaagacgcatgatgatgcagagtggtgag gtggaacggcaatacaaaggaacattagactgctttgtgaagatataccaacatgaggga atcagtgcattttttcgtggtgccttctccaatatccttcgtggtacagggggtgctttg gtattggtactatatgataaaattaaagaattccttaatattgatattggaggtagttca tcaggagattaa

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