KEGG   Piliocolobus tephrosceles (Ugandan red Colobus): 111546286
Entry
111546286         CDS       T07491                                 
Symbol
SLC25A31
Name
(RefSeq) ADP/ATP translocase 4 isoform X1
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
pteh  Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh04020  Calcium signaling pathway
pteh04022  cGMP-PKG signaling pathway
pteh04217  Necroptosis
pteh04218  Cellular senescence
pteh04613  Neutrophil extracellular trap formation
pteh05010  Alzheimer disease
pteh05012  Parkinson disease
pteh05016  Huntington disease
pteh05017  Spinocerebellar ataxia
pteh05020  Prion disease
pteh05022  Pathways of neurodegeneration - multiple diseases
pteh05164  Influenza A
pteh05166  Human T-cell leukemia virus 1 infection
pteh05208  Chemical carcinogenesis - reactive oxygen species
pteh05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:pteh00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    111546286 (SLC25A31)
   04022 cGMP-PKG signaling pathway
    111546286 (SLC25A31)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    111546286 (SLC25A31)
   04218 Cellular senescence
    111546286 (SLC25A31)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    111546286 (SLC25A31)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    111546286 (SLC25A31)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    111546286 (SLC25A31)
   05164 Influenza A
    111546286 (SLC25A31)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    111546286 (SLC25A31)
   05012 Parkinson disease
    111546286 (SLC25A31)
   05016 Huntington disease
    111546286 (SLC25A31)
   05017 Spinocerebellar ataxia
    111546286 (SLC25A31)
   05020 Prion disease
    111546286 (SLC25A31)
   05022 Pathways of neurodegeneration - multiple diseases
    111546286 (SLC25A31)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    111546286 (SLC25A31)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:pteh03029]
    111546286 (SLC25A31)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:pteh02000]
    111546286 (SLC25A31)
Mitochondrial biogenesis [BR:pteh03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    111546286 (SLC25A31)
Transporters [BR:pteh02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   111546286 (SLC25A31)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 111546286
NCBI-ProteinID: XP_023073386
Ensembl: ENSPTEG00000037370
UniProt: A0A8C9IUE0
LinkDB
Position
3:complement(61654002..61695064)
AA seq 315 aa
MHREPAKKKAEKRLFDASSFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQISPE
ARYKGMVDCLVRIPREQGFFSFWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVNKEKQ
FWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIMKIAKSD
GIAGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKKTPFLVSFFIAQVVTTCSGILS
YPFDTVRRRMMMQSGEAKRQYKGTLDCFVKIYQHEGINSFFRGAFSNVLRGTGGALVLVL
YDKLKEFFHIDIGGR
NT seq 948 nt   +upstreamnt  +downstreamnt
atgcatcgtgagccggcgaagaagaaggcagaaaagcggctgtttgatgcctcgtctttc
gggaaggaccttctggccggcggagtcgcggcagctgtgtccaagacagcggtggcgccc
atcgagcgggtgaagctgctgctgcaagtgcaggcgtcgtcgaagcagatcagcccagag
gcgcggtacaaaggcatggtggactgcctggtgcggattcctcgcgagcagggtttcttc
agtttttggcgtggcaatttggcaaatgttattaggtattttccaacacaagctttaaac
tttgcatttaaggacaaatacaagcagctattcatgtctggagttaataaagaaaaacag
ttctggaggtggtttttggcaaacctggcttctggtggagctgctggagcaacatcctta
tgtgtagtatatcctctagattttgcccgaacccgattaggtgtcgatattggaaaaggt
cctgaagagcgacaattcaagggtttaggtgactgtattatgaaaatagcaaaatcagat
ggaattgctggtttataccaagggtttggtgtttcagtacagggcatcattgtgtaccga
gcctcttattttggagcttatgacacagttaagggtttattaccaaagccaaagaaaact
ccatttcttgtctcctttttcattgctcaagttgtgactacatgctctggaatactttct
tatccctttgacacagttagaagacgtatgatgatgcagagtggtgaggctaaacggcaa
tataaaggaaccttagactgctttgtgaagatataccaacatgaaggaatcaattccttt
tttcgtggcgctttctccaatgtgcttcgtggtacagggggtgctttggtgttggtatta
tatgataaacttaaagaattctttcatatcgatattggtggtaggtaa

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