Ochotona princeps (American pika): 101522397 Help Entry 101522397         CDS       T07609                                  Symbol SLC25A31 Name (RefSeq) ADP/ATP translocase 4   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism opi  Ochotona princeps (American pika) Pathway opi04020   Calcium signaling pathway opi04022   cGMP-PKG signaling pathway opi04217   Necroptosis opi04218   Cellular senescence opi04613   Neutrophil extracellular trap formation opi05010   Alzheimer disease opi05012   Parkinson disease opi05016   Huntington disease opi05017   Spinocerebellar ataxia opi05020   Prion disease opi05022   Pathways of neurodegeneration - multiple diseases opi05164   Influenza A opi05166   Human T-cell leukemia virus 1 infection opi05208   Chemical carcinogenesis - reactive oxygen species opi05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:opi00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     101522397 (SLC25A31)    04022 cGMP-PKG signaling pathway     101522397 (SLC25A31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     101522397 (SLC25A31)    04218 Cellular senescence     101522397 (SLC25A31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     101522397 (SLC25A31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101522397 (SLC25A31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     101522397 (SLC25A31)    05164 Influenza A     101522397 (SLC25A31)   09164 Neurodegenerative disease    05010 Alzheimer disease     101522397 (SLC25A31)    05012 Parkinson disease     101522397 (SLC25A31)    05016 Huntington disease     101522397 (SLC25A31)    05017 Spinocerebellar ataxia     101522397 (SLC25A31)    05020 Prion disease     101522397 (SLC25A31)    05022 Pathways of neurodegeneration - multiple diseases     101522397 (SLC25A31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101522397 (SLC25A31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:opi03029]     101522397 (SLC25A31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:opi02000]     101522397 (SLC25A31) Mitochondrial biogenesis [BR:opi03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     101522397 (SLC25A31) Transporters [BR:opi02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    101522397 (SLC25A31) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  101522397 NCBI-ProteinID:  XP_004588261 LinkDB All DBs Position 15:complement(24614967..24632938) Genome browser AA seq 233 aa AA seqDB search MQREPARKKPEKHEKRLFDAMSFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQI SPEARYRGMVDCLVRIPQEQGMNAFFRGAFSNILRGTGGALVLVLYDKIKEFLNIDIGSP EERQFKGLGDCIVKIAKSDGIFGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETP FLISFFIAQIVTTCSGILSYPFDTVRRRMMMQVSLVIGEAILQTLSGTFRHKL NT seq 702 nt NT seq  +upstreamnt  +downstreamnt atgcagcgtgagcctgccagaaagaagcccgagaagcatgagaagcggctgtttgacgcc atgtccttcgggaaggacctgctggccggcggcgtggcggcagccgtgtccaagacggcg gtggcgcccatcgagcgggtgaagctgctgctgcaggtgcaggcgtcgtccaagcagatc agccccgaggcgcgctaccgaggcatggtggactgcttggtgcggattccccaggagcag ggaatgaatgcgtttttccgtggtgccttctccaatatccttcgtggtacaggcggtgct ttggtgttagtgttgtatgataaaattaaagaattccttaatattgatattggaagtcct gaagaacgacagttcaaaggtttaggtgactgtattgttaaaatagcaaaatcggatgga atatttggcttataccaaggatttggtgtttcagttcagggaatcattgtgtaccgagcc tcttactttggagcttatgatacagttaagggcttactaccaaaaccaaaagaaacgcca tttcttatctcatttttcattgctcagattgtgactacatgctctggaatactctcttat ccctttgatacagttagaagacggatgatgatgcaggtttccttagttattggcgaggca attttgcaaacgttatccggtactttccgacacaagctctaa

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