Pongo pygmaeus (Bornean orangutan): 129035041 Help Entry 129035041         CDS       T10128                                  Symbol SLC25A31 Name (RefSeq) ADP/ATP translocase 4   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism ppyg  Pongo pygmaeus (Bornean orangutan) Pathway ppyg04020   Calcium signaling pathway ppyg04022   cGMP-PKG signaling pathway ppyg04217   Necroptosis ppyg04218   Cellular senescence ppyg04613   Neutrophil extracellular trap formation ppyg05010   Alzheimer disease ppyg05012   Parkinson disease ppyg05016   Huntington disease ppyg05017   Spinocerebellar ataxia ppyg05020   Prion disease ppyg05022   Pathways of neurodegeneration - multiple diseases ppyg05164   Influenza A ppyg05166   Human T-cell leukemia virus 1 infection ppyg05208   Chemical carcinogenesis - reactive oxygen species ppyg05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:ppyg00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     129035041 (SLC25A31)    04022 cGMP-PKG signaling pathway     129035041 (SLC25A31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     129035041 (SLC25A31)    04218 Cellular senescence     129035041 (SLC25A31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     129035041 (SLC25A31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     129035041 (SLC25A31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     129035041 (SLC25A31)    05164 Influenza A     129035041 (SLC25A31)   09164 Neurodegenerative disease    05010 Alzheimer disease     129035041 (SLC25A31)    05012 Parkinson disease     129035041 (SLC25A31)    05016 Huntington disease     129035041 (SLC25A31)    05017 Spinocerebellar ataxia     129035041 (SLC25A31)    05020 Prion disease     129035041 (SLC25A31)    05022 Pathways of neurodegeneration - multiple diseases     129035041 (SLC25A31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     129035041 (SLC25A31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:ppyg03029]     129035041 (SLC25A31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:ppyg02000]     129035041 (SLC25A31) Mitochondrial biogenesis [BR:ppyg03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     129035041 (SLC25A31) Transporters [BR:ppyg02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    129035041 (SLC25A31) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  129035041 NCBI-ProteinID:  XP_054341038 LinkDB All DBs Position 3:140371359..140411959 Genome browser AA seq 315 aa AA seqDB search MHREPAKKKAEKRLFDASSFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQISPE ARYKGMVDCLVRIPREQGFFSFWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVNKEKQ FWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIMKIAKSD GIAGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKKTPFLVSFFIAQVVTTCSGILS YPFDTVRRRMMMQSGEAKRQYKGTLDCFVKIYQHEGISSFFRGAFSNVLRGTGGALVLVL YDKIKEFFHIDIGGR NT seq 948 nt NT seq  +upstreamnt  +downstreamnt atgcatcgtgagcctgcgaagaagaaggcagaaaagcggctgtttgacgcctcgtccttc gggaaggaccttctggccggcggagtcgcggcagctgtgtccaagacagcggtggcgccc atcgagcgggtgaagctgctgctgcaggtgcaggcgtcgtcgaagcagatcagccccgag gcgcggtacaaaggcatggtggactgcctggtgcggattcctcgcgagcagggtttcttc agtttttggcgtggcaatttggcaaatgttattcggtattttccaacacaagctctaaac tttgcttttaaggacaaatacaagcagctattcatgtctggagttaataaagaaaaacag ttctggaggtggtttttggcaaacctggcttctggtggagctgctggggcaacatcctta tgtgtagtatatcctctggattttgcccgaacccgattaggtgtcgatattggaaaaggt cctgaggaacgacaattcaagggtttaggtgactgtattatgaaaatagcaaaatcagat ggaattgctggtttataccaagggtttggtgtttcagtacagggcatcattgtgtaccga gcctcttattttggagcttatgacacagttaagggtttattaccaaagccaaagaaaact ccatttcttgtctcctttttcattgctcaagttgtgactacatgctctggaatactttct tatccctttgacacagttagaagacgtatgatgatgcagagtggtgaggctaaacggcaa tataaaggaaccttagactgctttgtgaagatataccaacatgaaggaatcagttccttt tttcgtggtgccttctccaatgttcttcgcggtacagggggtgctttggtgttggtatta tatgataaaatcaaagaattctttcatattgatattggtggtaggtaa

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