Phocoena sinus (vaquita): 116746997
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Entry
116746997 CDS
T07759
Symbol
SLC25A6
Name
(RefSeq) ADP/ATP translocase 3
KO
K05863
solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
psiu
Phocoena sinus (vaquita)
Pathway
psiu04020
Calcium signaling pathway
psiu04022
cGMP-PKG signaling pathway
psiu04217
Necroptosis
psiu04218
Cellular senescence
psiu04613
Neutrophil extracellular trap formation
psiu05010
Alzheimer disease
psiu05012
Parkinson disease
psiu05016
Huntington disease
psiu05017
Spinocerebellar ataxia
psiu05020
Prion disease
psiu05022
Pathways of neurodegeneration - multiple diseases
psiu05164
Influenza A
psiu05166
Human T-cell leukemia virus 1 infection
psiu05208
Chemical carcinogenesis - reactive oxygen species
psiu05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
psiu00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
116746997 (SLC25A6)
04022 cGMP-PKG signaling pathway
116746997 (SLC25A6)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
116746997 (SLC25A6)
04218 Cellular senescence
116746997 (SLC25A6)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
116746997 (SLC25A6)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
116746997 (SLC25A6)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
116746997 (SLC25A6)
05164 Influenza A
116746997 (SLC25A6)
09164 Neurodegenerative disease
05010 Alzheimer disease
116746997 (SLC25A6)
05012 Parkinson disease
116746997 (SLC25A6)
05016 Huntington disease
116746997 (SLC25A6)
05017 Spinocerebellar ataxia
116746997 (SLC25A6)
05020 Prion disease
116746997 (SLC25A6)
05022 Pathways of neurodegeneration - multiple diseases
116746997 (SLC25A6)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
116746997 (SLC25A6)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
psiu03029
]
116746997 (SLC25A6)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
psiu02000
]
116746997 (SLC25A6)
Mitochondrial biogenesis [BR:
psiu03029
]
Mitochondrial DNA transcription, translation, and replication factors
Mitochondrial transcription and translation factors
Other mitochondrial DNA transcription and translation factors
116746997 (SLC25A6)
Transporters [BR:
psiu02000
]
Solute carrier family (SLC)
SLC25: Mitochondrial carrier
116746997 (SLC25A6)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Mito_carr
Motif
Other DBs
NCBI-GeneID:
116746997
NCBI-ProteinID:
XP_032474703
Ensembl:
ENSPSNG00000020310
LinkDB
All DBs
Position
X:complement(815696..818831)
Genome browser
AA seq
298 aa
AA seq
DB search
MTEQAISFAKDFLAGGIAAAISKTAVAPIERVKLLLQVQHASKQIAADKQYKGIVDCIVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKHTQFWKYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKSGTEREFKGLGDCLVKITKSDGIRGLYQGFSVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNTHIVVSWMIAQTVTAVAGVVSYPFDTVRRRMMM
QSGRKGADIMYRGTLDCWRKIFKDEGGRAFFKGAWSNVLRGMGGAFVLVLYDELKKVI
NT seq
897 nt
NT seq
+upstream
nt +downstream
nt
atgacggaacaggccatctcattcgccaaggacttcctggccggaggcatcgccgccgcc
atctccaagacggccgtggccccgatcgagcgggtcaagctgctgctacaggtacagcac
gccagcaagcagatcgcggccgacaaacagtacaagggtatcgtggactgcatcgtgcgc
atccccaaggagcagggtgtgctgtccttctggaggggcaacctggccaatgtcatccgc
tacttccccacgcaagccctcaacttcgcctttaaggataagtataagcagatctttctg
gggggcgtggacaagcacacgcagttctggaagtacttcgccggcaacctggcctccggc
ggggcggccggagccacctccctctgctttgtctaccccctggatttcgccagaacccgg
ctggcggctgacgtcggcaaatccggcacggagcgggagttcaaaggcctgggagactgt
ctggtgaagattaccaagtctgacggcatccgggggctgtaccagggcttcagcgtctct
gtgcagggcatcatcatctaccgggccgcgtacttcggcgtgtatgacaccgccaaaggc
atgctccccgaccctaagaacacgcacatcgtggttagctggatgatcgcgcagacggtg
acggccgtggcgggcgtggtctcctaccccttcgacaccgtacggcggagaatgatgatg
cagtcggggcgcaaaggagccgacatcatgtacaggggcaccttggactgctggcgaaag
atcttcaaggacgagggcggcagagccttttttaagggcgcctggtccaacgtgctccgc
ggcatgggcggcgccttcgtgctggtcctgtatgatgagctgaagaaggtcatctag
DBGET
integrated database retrieval system