Mustela putorius furo (domestic ferret): 101688977
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Entry
101688977 CDS
T07239
Symbol
SLC25A5
Name
(RefSeq) ADP/ATP translocase 2
KO
K05863
solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
mpuf
Mustela putorius furo (domestic ferret)
Pathway
mpuf04020
Calcium signaling pathway
mpuf04022
cGMP-PKG signaling pathway
mpuf04217
Necroptosis
mpuf04218
Cellular senescence
mpuf04613
Neutrophil extracellular trap formation
mpuf05010
Alzheimer disease
mpuf05012
Parkinson disease
mpuf05016
Huntington disease
mpuf05017
Spinocerebellar ataxia
mpuf05020
Prion disease
mpuf05022
Pathways of neurodegeneration - multiple diseases
mpuf05164
Influenza A
mpuf05166
Human T-cell leukemia virus 1 infection
mpuf05208
Chemical carcinogenesis - reactive oxygen species
mpuf05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
mpuf00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
101688977 (SLC25A5)
04022 cGMP-PKG signaling pathway
101688977 (SLC25A5)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
101688977 (SLC25A5)
04218 Cellular senescence
101688977 (SLC25A5)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
101688977 (SLC25A5)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
101688977 (SLC25A5)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
101688977 (SLC25A5)
05164 Influenza A
101688977 (SLC25A5)
09164 Neurodegenerative disease
05010 Alzheimer disease
101688977 (SLC25A5)
05012 Parkinson disease
101688977 (SLC25A5)
05016 Huntington disease
101688977 (SLC25A5)
05017 Spinocerebellar ataxia
101688977 (SLC25A5)
05020 Prion disease
101688977 (SLC25A5)
05022 Pathways of neurodegeneration - multiple diseases
101688977 (SLC25A5)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
101688977 (SLC25A5)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
mpuf03029
]
101688977 (SLC25A5)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
mpuf02000
]
101688977 (SLC25A5)
Mitochondrial biogenesis [BR:
mpuf03029
]
Mitochondrial DNA transcription, translation, and replication factors
Mitochondrial transcription and translation factors
Other mitochondrial DNA transcription and translation factors
101688977 (SLC25A5)
Transporters [BR:
mpuf02000
]
Solute carrier family (SLC)
SLC25: Mitochondrial carrier
101688977 (SLC25A5)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Mito_carr
Motif
Other DBs
NCBI-GeneID:
101688977
NCBI-ProteinID:
XP_004762153
UniProt:
A0A8U0RJ69
LinkDB
All DBs
Position
Unknown
AA seq
298 aa
AA seq
DB search
MTDAAVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFKGLGDCLVKIYKSDGIRGLYQGFNVS
VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM
QSGRKGTDIMYTGTVDCWRKIARDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT
NT seq
897 nt
NT seq
+upstream
nt +downstream
nt
atgacagatgctgctgtgtccttcgccaaggacttcctggcgggtggagtggccgcggcc
atctccaagacggcggtagcgcccatcgagcgggtcaagctgctgctgcaggtgcagcat
gccagcaagcaaatcactgcggataagcaatacaagggcattatagactgcgtggttcgt
atccccaaggagcagggagtcctgtccttctggcgtggtaacctggccaatgtcatcaga
tacttccccacccaggctctcaactttgccttcaaagataaatacaagcagatcttcctg
ggtggcgtggacaaaagaacccagttttggcgctactttgccgggaatctggcatcgggt
ggtgcagctggggccacatccttgtgctttgtatatcctcttgattttgcccgtacccgc
ctagcagccgatgtgggcaaagccggagctgaaagggaattcaaaggcctcggtgactgc
ctggttaagatctacaaatctgatggcattaggggcctgtaccaaggcttcaatgtgtct
gtgcagggtattatcatctaccgagccgcctacttcggtatctatgacaccgccaaggga
atgcttccagatcccaagaatactcacatcttcatcagctggatgatcgcacagtctgtc
acagcggttgccgggttgacttcctatccatttgacactgttcgccgccgaatgatgatg
cagtctgggcgcaaagggactgacatcatgtacacaggcacagtggattgctggaggaag
atcgcgcgcgatgaaggcgccaaagcgtttttcaagggggcgtggtccaatgttctccgc
ggcatgggtggtgctttcgtgctcgtcttgtatgatgaaatcaagaagttcacataa
DBGET
integrated database retrieval system