KEGG   Equus caballus (horse): 100071908
Entry
100071908         CDS       T01058                                 
Symbol
SLC25A31
Name
(RefSeq) ADP/ATP translocase 4
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
ecb  Equus caballus (horse)
Pathway
ecb04020  Calcium signaling pathway
ecb04022  cGMP-PKG signaling pathway
ecb04217  Necroptosis
ecb04218  Cellular senescence
ecb04613  Neutrophil extracellular trap formation
ecb05010  Alzheimer disease
ecb05012  Parkinson disease
ecb05016  Huntington disease
ecb05017  Spinocerebellar ataxia
ecb05020  Prion disease
ecb05022  Pathways of neurodegeneration - multiple diseases
ecb05164  Influenza A
ecb05166  Human T-cell leukemia virus 1 infection
ecb05208  Chemical carcinogenesis - reactive oxygen species
ecb05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ecb00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100071908 (SLC25A31)
   04022 cGMP-PKG signaling pathway
    100071908 (SLC25A31)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100071908 (SLC25A31)
   04218 Cellular senescence
    100071908 (SLC25A31)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100071908 (SLC25A31)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100071908 (SLC25A31)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100071908 (SLC25A31)
   05164 Influenza A
    100071908 (SLC25A31)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100071908 (SLC25A31)
   05012 Parkinson disease
    100071908 (SLC25A31)
   05016 Huntington disease
    100071908 (SLC25A31)
   05017 Spinocerebellar ataxia
    100071908 (SLC25A31)
   05020 Prion disease
    100071908 (SLC25A31)
   05022 Pathways of neurodegeneration - multiple diseases
    100071908 (SLC25A31)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100071908 (SLC25A31)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ecb03029]
    100071908 (SLC25A31)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ecb02000]
    100071908 (SLC25A31)
Mitochondrial biogenesis [BR:ecb03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    100071908 (SLC25A31)
Transporters [BR:ecb02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   100071908 (SLC25A31)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 100071908
NCBI-ProteinID: XP_001502898
Ensembl: ENSECAG00000010831
VGNC: 23104
UniProt: F7DPW3
LinkDB
Position
2:complement(101505035..101538744)
AA seq 323 aa
MQREPPRRKPEKKAEKRLFDATSFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQ
ISPEARYKGMVDCLVRIPQEQGFFSYWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVN
KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGADIGKGPEERQFKGLGDCIMKI
AKSDGIVGLYRGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFVVSFFIAQVVTTCS
GILSYPFDTVRRRMMMQSGEAERQYKGTLDCFVKIYQHEGINAFFRGAFSNILRGTGGAL
VLVLYDKIKEFLNIDIGGSSSGD
NT seq 972 nt   +upstreamnt  +downstreamnt
atgcagcgtgaacctccgaggaggaagccggagaagaaggcagaaaagcggctctttgac
gccacgtccttcgggaaggacctgctggcaggcggggtcgcggcggccgtgtccaagacg
gcggtggcgcccatcgagcgggtgaagctgctgctgcaggtgcaggcgtcgtccaagcag
atcagccccgaggcgcggtacaaaggcatggtggactgcctggtgcggattccccaggag
cagggtttcttcagttattggcgtggcaatttggcaaatgttattcgatattttccgaca
caagctctaaactttgcttttaaggacaaatacaaacagcttttcatgtctggagttaat
aaagaaaaacagttctggaggtggtttttggcaaacctggcttctggtggagctgctggg
gcaacatccttatgtgtagtatatccgctagattttgcccgaacccgattaggtgccgat
attggaaaaggtcctgaagagcgacaattcaagggtttaggtgactgtatcatgaaaata
gcaaaatcagatggaattgttggtttataccgagggtttggtgtttcagttcagggcatc
attgtgtaccgagcctcttattttggagcttatgacacagttaagggtctattaccaaaa
ccaaaggaaaccccatttgttgtctcctttttcattgctcaagttgtgactacgtgctct
ggaatactctcttatccttttgacacagttagaagacgtatgatgatgcagagcggtgag
gctgaacggcaatataaaggaactttagactgctttgtgaagatataccaacatgaggga
atcaatgcattttttcgtggtgccttctccaacatccttcgtggtacagggggtgctttg
gtgttggtattatatgataaaattaaagaattccttaatattgatattggaggtagttca
tcaggagattaa

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