KEGG   Mustela nigripes (black-footed ferret): 132007616
Entry
132007616         CDS       T09425                                 
Symbol
SLC25A6
Name
(RefSeq) ADP/ATP translocase 3
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
mnp  Mustela nigripes (black-footed ferret)
Pathway
mnp04020  Calcium signaling pathway
mnp04022  cGMP-PKG signaling pathway
mnp04217  Necroptosis
mnp04218  Cellular senescence
mnp04613  Neutrophil extracellular trap formation
mnp05010  Alzheimer disease
mnp05012  Parkinson disease
mnp05016  Huntington disease
mnp05017  Spinocerebellar ataxia
mnp05020  Prion disease
mnp05022  Pathways of neurodegeneration - multiple diseases
mnp05164  Influenza A
mnp05166  Human T-cell leukemia virus 1 infection
mnp05208  Chemical carcinogenesis - reactive oxygen species
mnp05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:mnp00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    132007616 (SLC25A6)
   04022 cGMP-PKG signaling pathway
    132007616 (SLC25A6)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    132007616 (SLC25A6)
   04218 Cellular senescence
    132007616 (SLC25A6)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    132007616 (SLC25A6)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    132007616 (SLC25A6)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    132007616 (SLC25A6)
   05164 Influenza A
    132007616 (SLC25A6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    132007616 (SLC25A6)
   05012 Parkinson disease
    132007616 (SLC25A6)
   05016 Huntington disease
    132007616 (SLC25A6)
   05017 Spinocerebellar ataxia
    132007616 (SLC25A6)
   05020 Prion disease
    132007616 (SLC25A6)
   05022 Pathways of neurodegeneration - multiple diseases
    132007616 (SLC25A6)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    132007616 (SLC25A6)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:mnp03029]
    132007616 (SLC25A6)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:mnp02000]
    132007616 (SLC25A6)
Mitochondrial biogenesis [BR:mnp03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    132007616 (SLC25A6)
Transporters [BR:mnp02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   132007616 (SLC25A6)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 132007616
NCBI-ProteinID: XP_059241863
LinkDB
Position
X:123444937..123448333
AA seq 298 aa
MTEQAISFAKDFLAGGIAAAISKTAVAPIERVKLLLQVQHASKQIAADKQYKGIVDCIVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKHTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKSGTEREFKGLGDCLVKITKSDGIRGLYQGFNVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNTHIVVSWMIAQTVTAVAGVVSYPFDTVRRRMMM
QSGRKGADIMYKGTVDCWRKIFKDEGGKAFFKGAWSNVLRGMGGAFVLVLYDELKKVI
NT seq 897 nt   +upstreamnt  +downstreamnt
atgacggagcaggccatctccttcgccaaggacttcctggccgggggcatcgccgccgcc
atctccaagacggccgtggccccgatcgagcgggtcaagctgctgctgcaggtgcagcac
gccagcaagcagatcgctgcggacaagcagtacaagggcatcgtggactgcatcgtgcgg
atccccaaggagcagggtgtgctgtccttctggaggggcaacctggccaacgtcatccgc
tacttccccacgcaagcgctcaacttcgccttcaaggataagtacaagcagatcttcctg
ggcggcgtggacaagcacacgcagttctggaggtacttcgccgggaacctggcctcgggc
ggcgctgccggagccacctcgctctgcttcgtctacccgctggatttcgccagaacccgt
ctggctgccgatgtgggcaagtcgggcaccgagcgggagttcaagggcctgggagactgt
ctggtgaagatcaccaagtccgacggcatccggggcctctaccagggcttcaacgtgtcg
gtgcagggcatcatcatctaccgcgccgcctacttcggcgtgtacgacaccgccaagggc
atgctcccggaccccaagaacacccacatcgtggtgagctggatgatcgcgcagaccgtg
actgctgtggcaggcgtggtctcctacccctttgacaccgtgcggcggcggatgatgatg
cagtccgggcgcaaaggagcggacatcatgtacaagggcaccgtcgattgctggcggaag
atcttcaaagacgaagggggcaaggccttcttcaagggcgcgtggtccaacgtcctgagg
ggcatggggggcgcgttcgtgctggtcctctatgacgagctgaagaaggtcatctag

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