KEGG   Heterocephalus glaber (naked mole-rat): 101703823
Entry
101703823         CDS       T02812                                 
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
hgl  Heterocephalus glaber (naked mole-rat)
Pathway
hgl04020  Calcium signaling pathway
hgl04022  cGMP-PKG signaling pathway
hgl04217  Necroptosis
hgl04218  Cellular senescence
hgl04613  Neutrophil extracellular trap formation
hgl05010  Alzheimer disease
hgl05012  Parkinson disease
hgl05016  Huntington disease
hgl05017  Spinocerebellar ataxia
hgl05020  Prion disease
hgl05022  Pathways of neurodegeneration - multiple diseases
hgl05164  Influenza A
hgl05166  Human T-cell leukemia virus 1 infection
hgl05208  Chemical carcinogenesis - reactive oxygen species
hgl05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:hgl00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101703823 (Slc25a6)
   04022 cGMP-PKG signaling pathway
    101703823 (Slc25a6)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    101703823 (Slc25a6)
   04218 Cellular senescence
    101703823 (Slc25a6)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101703823 (Slc25a6)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101703823 (Slc25a6)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101703823 (Slc25a6)
   05164 Influenza A
    101703823 (Slc25a6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101703823 (Slc25a6)
   05012 Parkinson disease
    101703823 (Slc25a6)
   05016 Huntington disease
    101703823 (Slc25a6)
   05017 Spinocerebellar ataxia
    101703823 (Slc25a6)
   05020 Prion disease
    101703823 (Slc25a6)
   05022 Pathways of neurodegeneration - multiple diseases
    101703823 (Slc25a6)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101703823 (Slc25a6)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hgl03029]
    101703823 (Slc25a6)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hgl02000]
    101703823 (Slc25a6)
Mitochondrial biogenesis [BR:hgl03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    101703823 (Slc25a6)
Transporters [BR:hgl02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   101703823 (Slc25a6)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 101703823
NCBI-ProteinID: XP_004867368
UniProt: A0A0P6JGD2
LinkDB
Position
Un
AA seq 298 aa
MTEQAISFAKDFLAGGIAAAISKTAVAPIERVKLLLQVQHASKQIAAEKQYKGIVDCIVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKHTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKSGAEREFKGLGDCLVKITKSDGIRGLYQGFNVS
VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIVVSWMIAQSVTAVAGVVSYPFDTVRRRMMM
QSGRKGADIMYTGTIDCWRKILKDEGGKAFFKGAWSNVLRGMGGAFVLVLYDELKKVI
NT seq 897 nt   +upstreamnt  +downstreamnt
atgacggagcaggccatctccttcgccaaggacttcctggccgggggcatcgccgccgcc
atctccaagacggccgtggctccgatcgagcgggtcaagctgctgctgcaggtccagcat
gccagcaagcagatcgcggccgagaagcagtacaagggcatcgtggactgcatcgtgcgc
atccccaaggagcagggggtgctgtccttctggcgggggaacctggccaacgtcatccgc
tacttccccacgcaagccctcaacttcgccttcaaggacaagtacaagcagatcttcctg
ggcggcgtggacaagcacacgcagttctggcgctacttcgccggcaacctggcctcgggg
ggtgcggccggcgccacctccctgtgcttcgtgtacccgctggacttcgcccggacccgg
ctggccgccgacgttggcaagtcgggtgctgagcgcgagttcaagggcctgggtgactgt
ctggtgaagatcaccaagtcggatggcatccgcgggctctaccagggcttcaacgtgtcg
gtgcagggcatcatcatctaccgggccgcctacttcgggatctacgacaccgccaagggg
atgctgcccgaccccaagaacacgcacatcgtggtcagctggatgatcgcccagagcgtc
acggcggtggccggagtggtctcctacccgttcgacaccgtgcgccggcgcatgatgatg
cagtcaggccggaaaggggccgacatcatgtacacgggcaccatcgactgctggcgcaag
atcctcaaggacgagggcggcaaggccttcttcaagggcgcctggtccaacgtgctgcgg
ggcatgggcggcgccttcgtgctcgtgctgtacgacgagctcaagaaggtcatctag

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