Microcebus murinus (gray mouse lemur): 105885820 Help Entry 105885820         CDS       T07238                                  Symbol SLC25A31 Name (RefSeq) ADP/ATP translocase 4   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism mmur  Microcebus murinus (gray mouse lemur) Pathway mmur04020   Calcium signaling pathway mmur04022   cGMP-PKG signaling pathway mmur04217   Necroptosis mmur04218   Cellular senescence mmur04613   Neutrophil extracellular trap formation mmur05010   Alzheimer disease mmur05012   Parkinson disease mmur05016   Huntington disease mmur05017   Spinocerebellar ataxia mmur05020   Prion disease mmur05022   Pathways of neurodegeneration - multiple diseases mmur05164   Influenza A mmur05166   Human T-cell leukemia virus 1 infection mmur05208   Chemical carcinogenesis - reactive oxygen species mmur05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:mmur00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     105885820 (SLC25A31)    04022 cGMP-PKG signaling pathway     105885820 (SLC25A31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     105885820 (SLC25A31)    04218 Cellular senescence     105885820 (SLC25A31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     105885820 (SLC25A31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     105885820 (SLC25A31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     105885820 (SLC25A31)    05164 Influenza A     105885820 (SLC25A31)   09164 Neurodegenerative disease    05010 Alzheimer disease     105885820 (SLC25A31)    05012 Parkinson disease     105885820 (SLC25A31)    05016 Huntington disease     105885820 (SLC25A31)    05017 Spinocerebellar ataxia     105885820 (SLC25A31)    05020 Prion disease     105885820 (SLC25A31)    05022 Pathways of neurodegeneration - multiple diseases     105885820 (SLC25A31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     105885820 (SLC25A31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:mmur03029]     105885820 (SLC25A31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:mmur02000]     105885820 (SLC25A31) Mitochondrial biogenesis [BR:mmur03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     105885820 (SLC25A31) Transporters [BR:mmur02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    105885820 (SLC25A31) SSDB OrthologParalogGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  105885820 NCBI-ProteinID:  XP_012646522 Ensembl:  ENSMICG00000035863 UniProt:  A0A8B7I6J4 LinkDB All DBs Position 14:complement(69993725..70046475) Genome browser AA seq 319 aa AA seqDB search MQREPGKKKSEKRLFDAVSFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQISPE AQYKGMVDCLVRIPREQGFFSYWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVNKEKQ FWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIMKIAKSD GIIGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLISFFIAQVVTTCSGILS YPFDTVRRRMMMQSGEAERQYKGTLDCFAKIYQHEGIGAFFRGAFSNILRGTGGALVLVL YDKIKELLNIDIGGGSSGD NT seq 960 nt NT seq  +upstreamnt  +downstreamnt atgcagcgtgagcctgggaaaaagaagtctgaaaagcggctgtttgacgccgtgtccttc gggaaggacctgctggctggcggggtcgcggcggctgtgtccaagacggcggtggcgccc atcgagcgggtgaagctgctgctgcaggtgcaggcctcttcgaagcagatcagccccgag gcgcagtacaaaggcatggtggactgcctggtgcggattccccgagagcagggtttcttc agttattggcgtggcaatttggcaaatgttattcggtattttccaacacaagctctaaac tttgcttttaaggacaaatataaacaactattcatgtctggagttaataaagaaaaacag ttctggaggtggtttttggcaaacctggcttctggtggagctgctggagcaacatcctta tgtgtagtctatcctctagattttgcccgaacccgattaggtgtcgatatcggaaaaggt cctgaagagcgacagttcaagggtctaggagactgtattatgaaaattgcaaaatcagat ggaattattggtttataccaagggtttggtgtttcagttcagggtatcattgtataccga gcctcttattttggagcttatgacacagttaagggcttactgccaaaaccaaaggaaacc ccatttcttatctccttttttattgctcaagttgtgactacatgctctggaatactttct tatccctttgacacagttagaagacgtatgatgatgcagagtggtgaggctgaacggcaa tataaaggaaccttagactgctttgcgaagatataccaacatgagggaatcggcgcattt tttcgtggtgccttctctaatatccttcgtggtacagggggtgctttggtgttggtatta tatgataaaattaaagaattacttaatattgatattggaggtggttcatcaggagattaa

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