Cercocebus atys (sooty mangabey): 105587427 Help Entry 105587427         CDS       T07242                                  Symbol SLC25A31 Name (RefSeq) ADP/ATP translocase 4   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism caty  Cercocebus atys (sooty mangabey) Pathway caty04020   Calcium signaling pathway caty04022   cGMP-PKG signaling pathway caty04217   Necroptosis caty04218   Cellular senescence caty04613   Neutrophil extracellular trap formation caty05010   Alzheimer disease caty05012   Parkinson disease caty05016   Huntington disease caty05017   Spinocerebellar ataxia caty05020   Prion disease caty05022   Pathways of neurodegeneration - multiple diseases caty05164   Influenza A caty05166   Human T-cell leukemia virus 1 infection caty05208   Chemical carcinogenesis - reactive oxygen species caty05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:caty00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     105587427 (SLC25A31)    04022 cGMP-PKG signaling pathway     105587427 (SLC25A31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     105587427 (SLC25A31)    04218 Cellular senescence     105587427 (SLC25A31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     105587427 (SLC25A31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     105587427 (SLC25A31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     105587427 (SLC25A31)    05164 Influenza A     105587427 (SLC25A31)   09164 Neurodegenerative disease    05010 Alzheimer disease     105587427 (SLC25A31)    05012 Parkinson disease     105587427 (SLC25A31)    05016 Huntington disease     105587427 (SLC25A31)    05017 Spinocerebellar ataxia     105587427 (SLC25A31)    05020 Prion disease     105587427 (SLC25A31)    05022 Pathways of neurodegeneration - multiple diseases     105587427 (SLC25A31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     105587427 (SLC25A31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:caty03029]     105587427 (SLC25A31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:caty02000]     105587427 (SLC25A31) Mitochondrial biogenesis [BR:caty03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     105587427 (SLC25A31) Transporters [BR:caty02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    105587427 (SLC25A31) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  105587427 NCBI-ProteinID:  XP_011919044 Ensembl:  ENSCATG00000031744 UniProt:  A0A2K5LRH2 LinkDB All DBs Position Unknown AA seq 315 aa AA seqDB search MHREPPKKKAEKRLFDASSFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQISPE ARYKGMVDCLVRIPREQGFFSFWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVNKEKQ FWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIMKIAKSD GIAGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKKTPFLVSFFIAQVVTTCSGILS YPFDTVRRRMMMQSGEAKRQYKGTLDCFVKIYQHEGINSFFRGAFSNVLRGTGGALVLVL YDKIKEFFHIDIGGR NT seq 948 nt NT seq  +upstreamnt  +downstreamnt atgcatcgtgagcctccgaagaagaaggcagaaaagcgtctgtttgacgcctcgtctttc gggaaggaccttctggccggtggagtcgcggcagctgtgtccaagacagcagtggcgccc atcgagcgggtgaagctgctgctgcaagtgcaggcgtcgtcgaagcagatcagcccggag gcgcggtacaaaggcatggtggactgcctggtgcggattcctcgcgagcagggtttcttc agtttttggcgtggcaatttggcaaatgttattcggtattttccaacacaagctctaaac tttgcatttaaggacaaatacaagcagctcttcatgtctggagttaataaagaaaaacag ttctggaggtggtttttggcaaacctggcttctggtggagctgctggagcaacatcctta tgtgtagtatatcctctagattttgcccgaacccgattaggtgtcgatattggaaaaggt cctgaagagcgacaattcaagggtttaggtgactgtattatgaaaatagcaaaatcagat ggaattgctggtttataccaagggtttggtgtttcagtacagggcatcattgtgtaccga gcctcttattttggagcttatgacacagttaagggtttattaccaaagccaaagaaaact ccatttcttgtctcctttttcattgctcaagttgtgactacatgctctggaatactgtct tatccctttgacacagttagaagacgtatgatgatgcagagtggtgaggctaaacggcaa tataaaggaaccttagactgctttgtgaagatataccaacatgagggaatcaattccttt tttcgtggcgctttctccaatgttcttcgtggtacagggggtgctttggtgttggtatta tatgataaaattaaagaattctttcatatcgatattggtggtaggtaa

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