KEGG   Nannospalax galili (Upper Galilee mountains blind mole rat): 103750480
Entry
103750480         CDS       T03372                                 
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
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
    103750480 (Slc25a4)
   04022 cGMP-PKG signaling pathway
    103750480 (Slc25a4)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    103750480 (Slc25a4)
   04218 Cellular senescence
    103750480 (Slc25a4)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    103750480 (Slc25a4)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    103750480 (Slc25a4)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    103750480 (Slc25a4)
   05164 Influenza A
    103750480 (Slc25a4)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103750480 (Slc25a4)
   05012 Parkinson disease
    103750480 (Slc25a4)
   05016 Huntington disease
    103750480 (Slc25a4)
   05017 Spinocerebellar ataxia
    103750480 (Slc25a4)
   05020 Prion disease
    103750480 (Slc25a4)
   05022 Pathways of neurodegeneration - multiple diseases
    103750480 (Slc25a4)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    103750480 (Slc25a4)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ngi03029]
    103750480 (Slc25a4)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ngi02000]
    103750480 (Slc25a4)
Mitochondrial biogenesis [BR:ngi03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    103750480 (Slc25a4)
Transporters [BR:ngi02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   103750480 (Slc25a4)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 103750480
NCBI-ProteinID: XP_008851805
UniProt: A0A8C6QBA0
LinkDB
Position
Un
AA seq 298 aa
MGDQALSFVKDFLAGGIAAAVSKTAVAPIERVKLLLQVQHASKQISAEKQYKGIIDCVVR
IPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDRHKQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKGSAQREFSGLGDCLTKIFKSDGLKGLYQGFSVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNVHIIVSWMIAQSVTAVAGLVSYPFDTVRRRMMM
QSGRKGADIMYTGTLDCWRKIAKDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYV
NT seq 897 nt   +upstreamnt  +downstreamnt
atgggggatcaggctttgagcttcgtcaaggacttcctggcaggtggcatcgccgctgcc
gtctccaagactgcggtcgcccctatagagagggtcaaactgctgctgcaggtccagcat
gccagcaaacagatcagtgcagaaaaacagtacaaagggatcattgattgtgtcgttcga
atccccaaggagcagggctttctctctttctggaggggtaacctggccaatgtgatccgg
tatttccccacccaagctctcaacttcgccttcaaggacaagtacaagcagatcttcctg
gggggcgtggaccggcacaagcagttctggcgctactttgctgggaacctggcttccggt
ggggcagctggggccacctccctctgctttgtctacccgctggactttgctagaaccagg
ttggctgccgatgtgggcaagggttctgcccagcgtgagttcagtgggctgggcgactgt
ctcaccaagatcttcaagtctgatggcctgaagggtctctaccagggtttcagcgtctct
gtccagggcattatcatctacagagctgcctacttcggagtctatgatactgccaagggg
atgttgccagaccccaagaatgtgcacattattgtgagctggatgattgcacagagcgtg
acggcggtcgcagggctggtgtcctacccctttgacactgttcgtcgtaggatgatgatg
cagtctggccggaaaggggctgacattatgtatacggggacacttgattgctggaggaag
attgcaaaagatgaaggagccaaagctttcttcaaaggtgcctggtccaatgtattgaga
ggcatgggtggtgcttttgtattggtattgtatgatgagatcaaaaaatatgtctaa

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