Mustela nigripes (black-footed ferret): 132014518 Help Entry 132014518         CDS       T09425                                  Symbol SLC25A31 Name (RefSeq) ADP/ATP translocase 4 isoform X1   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism mnp  Mustela nigripes (black-footed ferret) Pathway mnp04020   Calcium signaling pathway mnp04022   cGMP-PKG signaling pathway mnp04217   Necroptosis mnp04218   Cellular senescence mnp04613   Neutrophil extracellular trap formation mnp05010   Alzheimer disease mnp05012   Parkinson disease mnp05016   Huntington disease mnp05017   Spinocerebellar ataxia mnp05020   Prion disease mnp05022   Pathways of neurodegeneration - multiple diseases mnp05164   Influenza A mnp05166   Human T-cell leukemia virus 1 infection mnp05208   Chemical carcinogenesis - reactive oxygen species mnp05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:mnp00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     132014518 (SLC25A31)    04022 cGMP-PKG signaling pathway     132014518 (SLC25A31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     132014518 (SLC25A31)    04218 Cellular senescence     132014518 (SLC25A31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     132014518 (SLC25A31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     132014518 (SLC25A31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     132014518 (SLC25A31)    05164 Influenza A     132014518 (SLC25A31)   09164 Neurodegenerative disease    05010 Alzheimer disease     132014518 (SLC25A31)    05012 Parkinson disease     132014518 (SLC25A31)    05016 Huntington disease     132014518 (SLC25A31)    05017 Spinocerebellar ataxia     132014518 (SLC25A31)    05020 Prion disease     132014518 (SLC25A31)    05022 Pathways of neurodegeneration - multiple diseases     132014518 (SLC25A31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     132014518 (SLC25A31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:mnp03029]     132014518 (SLC25A31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:mnp02000]     132014518 (SLC25A31) Mitochondrial biogenesis [BR:mnp03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     132014518 (SLC25A31) Transporters [BR:mnp02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    132014518 (SLC25A31) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  132014518 NCBI-ProteinID:  XP_059251485 LinkDB All DBs Position 1:188109778..188134377 Genome browser AA seq 320 aa AA seqDB search MQREPPKTKQEKKSEKRLFDPASFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQ ISAETQYKGMVDCLVRIPREQGFFSFWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVN KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGADIGKGPEERQFKGLGDCIIKI AKSDGIVGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLVSFFIAQVVTTCS GILSYPFDTVRRRMMMQSGEVERQYKGTLDCFVKIYQHEGISAFFRGAFSNILRGTGGAL VLVLYDKIKEFLNIDIGGSS NT seq 963 nt NT seq  +upstreamnt  +downstreamnt atgcagcgtgaacctccgaagacgaagcaagagaagaagtcggaaaagcggctctttgac cccgcgtccttcgggaaggacctgctggcaggcggggtcgcagcggctgtgtccaagacc gcggtggcccccatcgagcgggtgaagctgctgctgcaggtgcaggcgtcttccaagcag atcagtgccgagacgcagtacaaaggcatggtggactgcctggtgcggattccccgagag caaggtttcttcagtttttggcgtggcaatttggccaatgttatccgatattttccaaca caagctcttaactttgcgtttaaggacaaatacaaacaacttttcatgtctggagttaat aaagaaaagcagttctggaggtggtttttggcaaacctggcttctggtggagctgctgga gcaacatccttatgtgtagtttatccgctagactttgcccgaacccgattaggtgctgat attggaaaaggtcctgaagagcgacaattcaagggtttaggtgactgtattataaaaata gcaaaatcagacggaattgttggtttgtaccaagggtttggtgtttctgttcagggtatc attgtgtaccgagcctcctattttggagcatatgacacagttaagggcttattaccaaaa ccaaaggaaaccccatttcttgtctcctttttcattgctcaagttgtgaccacatgctct ggaattctttcttatccctttgacacagttagaagacgcatgatgatgcagagtggtgag gtggaacggcaatacaaaggaacattagactgctttgtgaagatataccaacatgaggga atcagtgcattttttcgtggtgccttctccaatatccttcgtggtacagggggtgctttg gtattggtactatatgataaaattaaagaattccttaatattgatattggaggtagttca taa

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