KEGG   Monodelphis domestica (gray short-tailed opossum): 100010639
Entry
100010639         CDS       T01031                                 
Symbol
SLC25A31
Name
(RefSeq) solute carrier family 25 member 31
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
mdo  Monodelphis domestica (gray short-tailed opossum)
Pathway
mdo04020  Calcium signaling pathway
mdo04022  cGMP-PKG signaling pathway
mdo04217  Necroptosis
mdo04218  Cellular senescence
mdo04613  Neutrophil extracellular trap formation
mdo05010  Alzheimer disease
mdo05012  Parkinson disease
mdo05016  Huntington disease
mdo05017  Spinocerebellar ataxia
mdo05020  Prion disease
mdo05022  Pathways of neurodegeneration - multiple diseases
mdo05164  Influenza A
mdo05166  Human T-cell leukemia virus 1 infection
mdo05208  Chemical carcinogenesis - reactive oxygen species
mdo05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:mdo00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100010639 (SLC25A31)
   04022 cGMP-PKG signaling pathway
    100010639 (SLC25A31)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100010639 (SLC25A31)
   04218 Cellular senescence
    100010639 (SLC25A31)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100010639 (SLC25A31)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100010639 (SLC25A31)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100010639 (SLC25A31)
   05164 Influenza A
    100010639 (SLC25A31)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100010639 (SLC25A31)
   05012 Parkinson disease
    100010639 (SLC25A31)
   05016 Huntington disease
    100010639 (SLC25A31)
   05017 Spinocerebellar ataxia
    100010639 (SLC25A31)
   05020 Prion disease
    100010639 (SLC25A31)
   05022 Pathways of neurodegeneration - multiple diseases
    100010639 (SLC25A31)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100010639 (SLC25A31)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:mdo03029]
    100010639 (SLC25A31)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:mdo02000]
    100010639 (SLC25A31)
Mitochondrial biogenesis [BR:mdo03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    100010639 (SLC25A31)
Transporters [BR:mdo02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   100010639 (SLC25A31)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 100010639
NCBI-ProteinID: XP_001363920
Ensembl: ENSMODG00000012128
UniProt: F7FU45
LinkDB
Position
5:1137142..1178812
AA seq 314 aa
MVGRRSEQTQGQLLSFGKDLLAGGIAAAVSKTAVAPIERVKLLLQVQASSKQISPEAQYK
GMVDCFVRIPREQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFMSGVNKDKQFWRW
FMANLASGGAAGATSLCVVYPLDFARTRLGADIGKGLEERQFKGLGDCIVKIAKSDGITG
LYQGFGVSVQGIIVYRASYFGSYDTIKGLLANPRDTPFLVSFFIAQVVTTCSGIISYPFD
TVRRRMMMQSGEAERQYKGTIDCFVKIYQHEGFGAFFRGAFSNVLRGTGGALVLVLYDKI
KELLNIDIGGSSVE
NT seq 945 nt   +upstreamnt  +downstreamnt
atggtgggcaggcgctctgagcagacccaggggcagctgctgtcctttggcaaggatctg
ctggctggcggcattgcggctgccgtgtccaagacggccgtggcgcccatcgagcgggtg
aagctgctgctgcaggtgcaagcgtcgtccaagcagatcagccccgaggcgcagtacaag
ggcatggtggactgcttcgtgcgcatcccgcgggaacagggttttctcagtttttggcgt
ggcaatttggcaaatgttattcgatattttccaacacaagctctaaactttgcttttaag
gacaaatacaaacagattttcatgtcaggagttaacaaagataaacagttctggaggtgg
tttatggctaatctagcctcaggcggagctgcaggggcgacatccctatgtgtggtgtat
ccactagattttgcccgaactcgattaggggctgatattggaaaaggtcttgaagaacgg
cagttcaaaggtttaggtgattgcattgtcaagatagcaaaatctgatggcatcactggt
ttataccaaggatttggggtttctgttcaaggtatcattgtgtatcgagcctcctatttt
ggatcttatgacacaattaagggcttattggcaaatccaagggacaccccattccttgtg
tcctttttcatcgctcaagttgtaactacttgctccggaataatctcttatccctttgac
accgtcagaaggcgcatgatgatgcagagtggcgaggcggagcgccagtacaagggaacc
atcgactgctttgtgaagatataccaacacgaaggcttcggggctttcttccgtggagcc
ttctccaatgtcctccgaggcacaggcggtgccttagtgctggtcttgtatgataaaatc
aaagagctgttaaatattgacattggaggcagttcagtggaataa

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