KEGG   Myotis davidii (David's myotis): 102774608
Entry
102774608         CDS       T02992                                 
Symbol
SLC25A4
Name
(RefSeq) solute carrier family 25 member 4
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
myd  Myotis davidii (David's myotis)
Pathway
myd04020  Calcium signaling pathway
myd04022  cGMP-PKG signaling pathway
myd04217  Necroptosis
myd04218  Cellular senescence
myd04613  Neutrophil extracellular trap formation
myd05010  Alzheimer disease
myd05012  Parkinson disease
myd05016  Huntington disease
myd05017  Spinocerebellar ataxia
myd05020  Prion disease
myd05022  Pathways of neurodegeneration - multiple diseases
myd05164  Influenza A
myd05166  Human T-cell leukemia virus 1 infection
myd05208  Chemical carcinogenesis - reactive oxygen species
myd05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:myd00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    102774608 (SLC25A4)
   04022 cGMP-PKG signaling pathway
    102774608 (SLC25A4)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    102774608 (SLC25A4)
   04218 Cellular senescence
    102774608 (SLC25A4)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    102774608 (SLC25A4)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    102774608 (SLC25A4)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    102774608 (SLC25A4)
   05164 Influenza A
    102774608 (SLC25A4)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102774608 (SLC25A4)
   05012 Parkinson disease
    102774608 (SLC25A4)
   05016 Huntington disease
    102774608 (SLC25A4)
   05017 Spinocerebellar ataxia
    102774608 (SLC25A4)
   05020 Prion disease
    102774608 (SLC25A4)
   05022 Pathways of neurodegeneration - multiple diseases
    102774608 (SLC25A4)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    102774608 (SLC25A4)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:myd03029]
    102774608 (SLC25A4)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:myd02000]
    102774608 (SLC25A4)
Mitochondrial biogenesis [BR:myd03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    102774608 (SLC25A4)
Transporters [BR:myd02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   102774608 (SLC25A4)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 102774608
NCBI-ProteinID: XP_015425256
LinkDB
Position
Un
AA seq 252 aa
MSDQALSFLKDFLAGGIAAXXXXQICARPQALRASLQVQHASKQISAEQQYKGIMDCVVR
IPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDRHKQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKGSAQREFSGLGDCLTKIFKSDGLGGLYQGFSVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNVHIFISWMIAQSVTAVAGLVSYPFDTVRRRMMM
QSGRKGGKPGTY
NT seq 759 nt   +upstreamnt  +downstreamnt
atgagtgatcaggctctgagcttcctgaaggacttcctggctggtggcatcgccgctnnn
nnnnnnnagcagatctgcgctaggccacaggccctgcgcgcctccctgcaggtccagcat
gccagcaaacagatcagcgctgagcaacagtacaaagggatcatggattgcgtggtgaga
atccccaaggagcagggctttctctccttctggagaggtaacctggccaacgtgatccgt
tacttccccacccaagctctcaacttcgccttcaaggacaagtacaagcagatcttcctg
gggggcgtggaccggcacaagcagttctggcgctactttgccggtaacctggcttctggt
ggggcagctggggccacctccctctgctttgtctacccgctggacttcgccaggaccagg
ttggctgccgacgtgggcaagggtagcgcccagcgtgagttcagtggtctgggcgactgt
ctcaccaagatcttcaagtccgatggccttgggggtctctaccagggtttcagcgtctct
gtccagggcatcattatctacagagctgcctacttcggagtctatgatactgccaagggg
atgctgcctgaccccaagaatgtgcacattttcatcagctggatgatcgctcagtccgtg
acggcggtggcggggctggtgtcctacccctttgacactgtgcgccgtaggatgatgatg
cagtctggccggaaggggggtaagcctggcacctactga

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