Eulemur rufifrons (Bennett's brown lemur): 138377792
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Entry
138377792 CDS
T11398
Symbol
SLC25A6
Name
(RefSeq) ADP/ATP translocase 3
KO
K05863
solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
eruf Eulemur rufifrons (Bennett's brown lemur)
Pathway
eruf04020
Calcium signaling pathway
eruf04022
cGMP-PKG signaling pathway
eruf04217
Necroptosis
eruf04218
Cellular senescence
eruf04613
Neutrophil extracellular trap formation
eruf05010
Alzheimer disease
eruf05012
Parkinson disease
eruf05016
Huntington disease
eruf05017
Spinocerebellar ataxia
eruf05020
Prion disease
eruf05022
Pathways of neurodegeneration - multiple diseases
eruf05164
Influenza A
eruf05166
Human T-cell leukemia virus 1 infection
eruf05208
Chemical carcinogenesis - reactive oxygen species
eruf05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
eruf00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
138377792 (SLC25A6)
04022 cGMP-PKG signaling pathway
138377792 (SLC25A6)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
138377792 (SLC25A6)
04218 Cellular senescence
138377792 (SLC25A6)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
138377792 (SLC25A6)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
138377792 (SLC25A6)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
138377792 (SLC25A6)
05164 Influenza A
138377792 (SLC25A6)
09164 Neurodegenerative disease
05010 Alzheimer disease
138377792 (SLC25A6)
05012 Parkinson disease
138377792 (SLC25A6)
05016 Huntington disease
138377792 (SLC25A6)
05017 Spinocerebellar ataxia
138377792 (SLC25A6)
05020 Prion disease
138377792 (SLC25A6)
05022 Pathways of neurodegeneration - multiple diseases
138377792 (SLC25A6)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
138377792 (SLC25A6)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
eruf03029
]
138377792 (SLC25A6)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
eruf02000
]
138377792 (SLC25A6)
Mitochondrial biogenesis [BR:
eruf03029
]
Mitochondrial DNA transcription, translation, and replication factors
Mitochondrial transcription and translation factors
Other mitochondrial DNA transcription and translation factors
138377792 (SLC25A6)
Transporters [BR:
eruf02000
]
Solute carrier family (SLC)
SLC25: Mitochondrial carrier
138377792 (SLC25A6)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Mito_carr
Motif
Other DBs
NCBI-GeneID:
138377792
NCBI-ProteinID:
XP_069318886
LinkDB
All DBs
Position
30:143599513..143602864
Genome browser
AA seq
298 aa
AA seq
DB search
MTEQAISFAKDFLAGGIAAAISKTAVAPIERVKLLLQVQHASKQIAADKQYKGIVDCIVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKHTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKSGTEREFKGLGDCLVKITKSDGIRGLYQGFNVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNTHIVVSWMIAQTVTAVAGVVSYPFDTVRRRMMM
QSGRKGADIMYRGTLDCWRKIFRDEGGKAFFKGAWSNVLRGMGGAFVLVLYDELKKVI
NT seq
897 nt
NT seq
+upstream
nt +downstream
nt
atgacggaacaggccatctccttcgccaaggacttcctggccgggggcatcgccgccgcc
atctccaagacggccgtggccccgatcgagagggtcaagctgctgctgcaggtgcaacac
gccagcaagcagatcgcggccgacaagcagtacaagggcatcgtggactgcatcgtgcgc
atccccaaggagcagggcgtgctgtccttctggaggggcaacctggccaacgtgatccgc
tacttccccacgcaagccctcaacttcgccttcaaggataagtacaagcagatcttcctg
gggggcgtggacaagcacacgcagttctggaggtattttgccggcaacctggcgtccgga
ggggcggccggggccacgtccctctgcttcgtgtacccgctggatttcgccaggacccgc
ctggctgccgacgtgggcaagtcgggcaccgagcgggagttcaagggcctgggagactgt
ctggtgaagatcaccaagtccgacggcatccggggcctgtatcagggcttcaacgtgtcc
gtgcagggcatcatcatctaccgggcggcctacttcggcgtctacgacacggctaaaggc
atgcttccggaccccaagaacacgcacatcgtggtgagctggatgatagcccagaccgtg
acggccgtggccggcgtggtctcctaccccttcgacaccgtgcggcggcggatgatgatg
cagtctgggcgcaaaggagctgacatcatgtacagggggaccctggactgctggaggaag
atcttcagagacgaaggtggcaaagccttcttcaagggcgcctggtccaatgtcctcagg
ggcatggggggcgccttcgtgctggtcttgtacgacgagcttaagaaagtcatctaa
DBGET
integrated database retrieval system