Heterocephalus glaber (naked mole-rat): 101698774 Help Entry 101698774         CDS       T02812                                  Symbol Slc25a31 Name (RefSeq) ADP/ATP translocase 4   KO K05863   solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31 Organism hgl  Heterocephalus glaber (naked mole-rat) Pathway hgl04020   Calcium signaling pathway hgl04022   cGMP-PKG signaling pathway hgl04217   Necroptosis hgl04218   Cellular senescence hgl04613   Neutrophil extracellular trap formation hgl05010   Alzheimer disease hgl05012   Parkinson disease hgl05016   Huntington disease hgl05017   Spinocerebellar ataxia hgl05020   Prion disease hgl05022   Pathways of neurodegeneration - multiple diseases hgl05164   Influenza A hgl05166   Human T-cell leukemia virus 1 infection hgl05208   Chemical carcinogenesis - reactive oxygen species hgl05415   Diabetic cardiomyopathy Brite KEGG Orthology (KO) [BR:hgl00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     101698774 (Slc25a31)    04022 cGMP-PKG signaling pathway     101698774 (Slc25a31)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     101698774 (Slc25a31)    04218 Cellular senescence     101698774 (Slc25a31)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     101698774 (Slc25a31)  09160 Human Diseases   09161 Cancer: overview    05208 Chemical carcinogenesis - reactive oxygen species     101698774 (Slc25a31)   09172 Infectious disease: viral    05166 Human T-cell leukemia virus 1 infection     101698774 (Slc25a31)    05164 Influenza A     101698774 (Slc25a31)   09164 Neurodegenerative disease    05010 Alzheimer disease     101698774 (Slc25a31)    05012 Parkinson disease     101698774 (Slc25a31)    05016 Huntington disease     101698774 (Slc25a31)    05017 Spinocerebellar ataxia     101698774 (Slc25a31)    05020 Prion disease     101698774 (Slc25a31)    05022 Pathways of neurodegeneration - multiple diseases     101698774 (Slc25a31)   09166 Cardiovascular disease    05415 Diabetic cardiomyopathy     101698774 (Slc25a31)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:hgl03029]     101698774 (Slc25a31)   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hgl02000]     101698774 (Slc25a31) Mitochondrial biogenesis [BR:hgl03029]  Mitochondrial DNA transcription, translation, and replication factors   Mitochondrial transcription and translation factors    Other mitochondrial DNA transcription and translation factors     101698774 (Slc25a31) Transporters [BR:hgl02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    101698774 (Slc25a31) SSDB OrthologParalogGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  101698774 NCBI-ProteinID:  XP_004855012 UniProt:  G5AKY3 LinkDB All DBs Position Unknown AA seq 323 aa AA seqDB search MQREPAKKKPEKKAEKPLFDAASFRKDLLAGGIAAAVSKTAVAPIERVKLLLQVQVSSKQ ISPEARYKGMVDCLVRIPREQGFFSYWRGNLANVIRYFPTQALNFAFKDKYKQIFMSGVN KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIVKI AKSDGIVGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLVSFFIAQVVTTCS GILSYPFDTVRRRMMMQSGEAERQYKGTLDCFVKIYRHEGINAFFRGAFSNILRGTGGAL VLVLYDKIKELFNIDIKGGSSGD NT seq 972 nt NT seq  +upstreamnt  +downstreamnt atgcagcgtgagcctgctaagaagaagccggagaagaaggcagaaaagccgttgtttgac gctgcatcctttcggaaggacctgctggctggcgggatcgccgcggctgtgtccaagaca gccgtggctcccatagagcgagtgaagctgctgttgcaggtgcaggtgtcgtcgaagcag atcagtcccgaagcacggtacaaaggcatggtggactgcctggtgcggattcctcgcgaa cagggtttcttcagttattggagaggcaatctggcaaatgttatccgatattttccaaca caagctctaaactttgcttttaaggacaaatacaagcaaatcttcatgtctggagttaat aaagaaaaacagttctggagatggtttttggcaaacctggcttctggtggagctgctggg gcaacatccttgtgtgttgtgtatccactagattttgcccgaacccggttaggtgttgat attggaaaaggccctgaagagcgacaattcaagggtttaggtgactgtattgtgaaaata gcaaaatcagatggaattgttggtttataccaagggtttggtgtttcagttcaggggatc attgtgtaccgagcctcttattttggagcttatgacacagttaagggcttattaccaaaa ccaaaggaaaccccatttcttgtctcgtttttcattgctcaagttgtgaccacatgctct ggaatactgtcttatccctttgacacagttagaagacgcatgatgatgcagagtggtgag gctgaacggcagtacaaaggaaccttagattgctttgtgaagatataccgacatgaggga atcaatgcattttttcgtggtgccttttccaacatccttcgtggtacaggaggtgctttg gtgttggtgttatatgataaaattaaagaattgtttaatattgatatcaaaggtggttca tcaggagattaa

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