KEGG   Nannospalax galili (Upper Galilee mountains blind mole rat): 103742868
Entry
103742868         CDS       T03372                                 
Symbol
Slc25a5
Name
(RefSeq) solute carrier family 25 member 5
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
ngi  Nannospalax galili (Upper Galilee mountains blind mole rat)
Pathway
ngi04020  Calcium signaling pathway
ngi04022  cGMP-PKG signaling pathway
ngi04217  Necroptosis
ngi04218  Cellular senescence
ngi04613  Neutrophil extracellular trap formation
ngi05010  Alzheimer disease
ngi05012  Parkinson disease
ngi05016  Huntington disease
ngi05017  Spinocerebellar ataxia
ngi05020  Prion disease
ngi05022  Pathways of neurodegeneration - multiple diseases
ngi05164  Influenza A
ngi05166  Human T-cell leukemia virus 1 infection
ngi05208  Chemical carcinogenesis - reactive oxygen species
ngi05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ngi00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    103742868 (Slc25a5)
   04022 cGMP-PKG signaling pathway
    103742868 (Slc25a5)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    103742868 (Slc25a5)
   04218 Cellular senescence
    103742868 (Slc25a5)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    103742868 (Slc25a5)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    103742868 (Slc25a5)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    103742868 (Slc25a5)
   05164 Influenza A
    103742868 (Slc25a5)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103742868 (Slc25a5)
   05012 Parkinson disease
    103742868 (Slc25a5)
   05016 Huntington disease
    103742868 (Slc25a5)
   05017 Spinocerebellar ataxia
    103742868 (Slc25a5)
   05020 Prion disease
    103742868 (Slc25a5)
   05022 Pathways of neurodegeneration - multiple diseases
    103742868 (Slc25a5)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    103742868 (Slc25a5)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ngi03029]
    103742868 (Slc25a5)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ngi02000]
    103742868 (Slc25a5)
Mitochondrial biogenesis [BR:ngi03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    103742868 (Slc25a5)
Transporters [BR:ngi02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   103742868 (Slc25a5)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 103742868
NCBI-ProteinID: XP_008842240
UniProt: A0A8C6QXG6
LinkDB
Position
Un
AA seq 298 aa
MTDAAVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFKGLGDCLVKIYKSDGIKGLYQGFNVS
VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM
QSGRKGTDIMYTGTLDCWRKIARDEGSKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT
NT seq 897 nt   +upstreamnt  +downstreamnt
atgacagatgccgctgtgtccttcgccaaggacttcctggcaggtggagtggcggcggcc
atctccaagaccgcagtagcgcccatcgagcgggtcaagctgctgctgcaggtgcagcat
gccagcaagcaaatcacagcagataagcaatacaagggcattatagactgcgtggttcgt
atccccaaggaacagggagtcctgtccttctggcgtggtaacctggccaatgtcatcaga
tacttccccacccaggctctcaactttgccttcaaagataaatacaagcagatcttcctg
ggtggtgtggacaagaggacccagttttggcgctactttgcagggaacctggcatcgggt
ggtgccgctggggccacatccttgtgctttgtgtaccctcttgattttgcccgtacccgt
ctagcagctgatgttggcaaagctggagccgaaagggaattcaaaggccttggtgactgc
ctggttaagatctacaaatctgatgggattaagggcctgtaccaaggctttaatgtatct
gtgcagggtattatcatctaccgagctgcctactttggtatctatgatactgcaaaggga
atgcttccagatcccaagaatactcacatcttcatcagctggatgattgcacagtctgtc
accgccgttgctggcttgacttcctatccctttgatacggttcgtcgtcgcatgatgatg
cagtcaggacgcaaaggaactgacatcatgtacacaggcacacttgactgctggaggaag
attgctcgtgatgaaggaagcaaagcttttttcaagggtgcatggtccaatgttctcaga
ggcatgggtggtgcttttgtgcttgtcttgtatgatgaaatcaagaagttcacataa

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