KEGG   Panthera tigris altaica (Amur tiger): 102966182
Entry
102966182         CDS       T02988                                 
Symbol
SLC25A6
Name
(RefSeq) solute carrier family 25 member 6
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
ptg  Panthera tigris altaica (Amur tiger)
Pathway
ptg04020  Calcium signaling pathway
ptg04022  cGMP-PKG signaling pathway
ptg04217  Necroptosis
ptg04218  Cellular senescence
ptg04613  Neutrophil extracellular trap formation
ptg05010  Alzheimer disease
ptg05012  Parkinson disease
ptg05016  Huntington disease
ptg05017  Spinocerebellar ataxia
ptg05020  Prion disease
ptg05022  Pathways of neurodegeneration - multiple diseases
ptg05164  Influenza A
ptg05166  Human T-cell leukemia virus 1 infection
ptg05208  Chemical carcinogenesis - reactive oxygen species
ptg05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ptg00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    102966182 (SLC25A6)
   04022 cGMP-PKG signaling pathway
    102966182 (SLC25A6)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    102966182 (SLC25A6)
   04218 Cellular senescence
    102966182 (SLC25A6)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    102966182 (SLC25A6)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    102966182 (SLC25A6)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    102966182 (SLC25A6)
   05164 Influenza A
    102966182 (SLC25A6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102966182 (SLC25A6)
   05012 Parkinson disease
    102966182 (SLC25A6)
   05016 Huntington disease
    102966182 (SLC25A6)
   05017 Spinocerebellar ataxia
    102966182 (SLC25A6)
   05020 Prion disease
    102966182 (SLC25A6)
   05022 Pathways of neurodegeneration - multiple diseases
    102966182 (SLC25A6)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    102966182 (SLC25A6)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ptg03029]
    102966182 (SLC25A6)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ptg02000]
    102966182 (SLC25A6)
Mitochondrial biogenesis [BR:ptg03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    102966182 (SLC25A6)
Transporters [BR:ptg02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   102966182 (SLC25A6)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 102966182
NCBI-ProteinID: XP_007091091
LinkDB
Position
Un
AA seq 274 aa
WGPVASARPPALQVQHASKQIAADKQYKGIVDCIVRIPKEQGVLSFWRGNLANVIRYFPT
QALNFAFKDKYKQIFLGGVDKHTQFWRYFAGNLASGGAAGATSLCFVYPLDFARTRLAAD
VGKSGTEREFKGLGDCLVKITKSDGIRGLYQGFNVSVQGIIIYRAAYFGVYDTAKGMLPD
PKNTHIVVSWMIAQTVTAVAGVVSYPFDTVRRRMMMQSGRKGADIMYKGTLDCWRKIFKD
EGGKAFFKGAWSNVLRGMGGAFVLVLYDELKKVL
NT seq 825 nt   +upstreamnt  +downstreamnt
tggggccctgttgccagcgcgcgcccgcccgccctgcaggtgcagcacgccagcaagcag
atcgccgccgacaagcagtacaagggcatcgtggactgcatcgtgcgcatccccaaggag
cagggcgtcctgtccttctggaggggcaacctggccaacgtcatccgctacttccccacg
caagcgctcaacttcgccttcaaggataagtacaagcagatcttcctggggggcgtggac
aagcacacgcagttctggaggtacttcgccggcaacctggcgtcgggcggggcggccgga
gccacgtcgctgtgcttcgtgtacccgctggatttcgccaggacccgtctggccgccgac
gtgggcaagtcgggcaccgagcgggagttcaagggcctgggagactgcctggtcaagatc
accaagtctgacggcatccgcggcctgtaccagggcttcaacgtgtcggtgcagggcatc
atcatctaccgggcggcctacttcggcgtgtacgacacggccaaaggcatgctcccggac
cccaagaacacccacatcgtggtgagctggatgatcgcgcagacggtgacggccgtggcg
ggcgtggtctcctaccccttcgacaccgtgcggaggcgcatgatgatgcagtcggggcgc
aaaggagccgacatcatgtacaaggggaccctcgactgctggcggaagatcttcaaagac
gaagggggcaaagccttcttcaagggtgcgtggtccaacgtcctgcggggcatggggggc
gcctttgtgctcgtgctgtacgacgagctgaagaaagttctctag

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