Mirounga angustirostris (Northern elephant seal): 123849080
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Entry
123849080 CDS
T11530
Symbol
SLC25A5
Name
(RefSeq) ADP/ATP translocase 2
KO
K05863
solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
mano Mirounga angustirostris (Northern elephant seal)
Pathway
mano04020
Calcium signaling pathway
mano04022
cGMP-PKG signaling pathway
mano04217
Necroptosis
mano04218
Cellular senescence
mano04613
Neutrophil extracellular trap formation
mano05010
Alzheimer disease
mano05012
Parkinson disease
mano05016
Huntington disease
mano05017
Spinocerebellar ataxia
mano05020
Prion disease
mano05022
Pathways of neurodegeneration - multiple diseases
mano05164
Influenza A
mano05166
Human T-cell leukemia virus 1 infection
mano05208
Chemical carcinogenesis - reactive oxygen species
mano05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
mano00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
123849080 (SLC25A5)
04022 cGMP-PKG signaling pathway
123849080 (SLC25A5)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
123849080 (SLC25A5)
04218 Cellular senescence
123849080 (SLC25A5)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
123849080 (SLC25A5)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
123849080 (SLC25A5)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
123849080 (SLC25A5)
05164 Influenza A
123849080 (SLC25A5)
09164 Neurodegenerative disease
05010 Alzheimer disease
123849080 (SLC25A5)
05012 Parkinson disease
123849080 (SLC25A5)
05016 Huntington disease
123849080 (SLC25A5)
05017 Spinocerebellar ataxia
123849080 (SLC25A5)
05020 Prion disease
123849080 (SLC25A5)
05022 Pathways of neurodegeneration - multiple diseases
123849080 (SLC25A5)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
123849080 (SLC25A5)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
mano03029
]
123849080 (SLC25A5)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
mano02000
]
123849080 (SLC25A5)
Mitochondrial biogenesis [BR:
mano03029
]
Mitochondrial DNA transcription, translation, and replication factors
Mitochondrial transcription and translation factors
Other mitochondrial DNA transcription and translation factors
123849080 (SLC25A5)
Transporters [BR:
mano02000
]
Solute carrier family (SLC)
SLC25: Mitochondrial carrier
123849080 (SLC25A5)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Mito_carr
Motif
Other DBs
NCBI-GeneID:
123849080
NCBI-ProteinID:
XP_045737799
LinkDB
All DBs
Position
Unknown
AA seq
298 aa
AA seq
DB search
MTDAAVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFRGLGDCLVKIYKSDGIKGLYQGFNVS
VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM
QSGRKGTDIMYTGTIDCWRKIARDEGGKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT
NT seq
897 nt
NT seq
+upstream
nt +downstream
nt
atgacagatgccgctgtgtccttcgccaaggacttcctggcgggtggagtggccgcggcc
atctccaagacggcggtagcgcccatcgagcgggtcaagctgctgctgcaggtgcagcat
gcgagcaagcaaatcaccgcagataagcaatacaagggcattatagactgtgtggttcgc
atccccaaggagcagggagtcctgtccttctggcgcggtaacctggccaatgtcatcaga
tacttcccgacccaggctctcaacttcgccttcaaagataaatacaagcagatcttcctg
ggtggtgtggacaagagaacccagttttggcgctactttgctgggaatctggcgtcaggt
ggtgccgctggggccacgtccttgtgttttgtgtatcctcttgattttgcccgtacccgg
ctagcagccgatgtgggcaaagctggagctgaaagggaattcagaggcctcggtgactgc
ctggttaagatctacaaatctgatgggattaagggcctgtaccaaggctttaatgtgtct
gtgcagggcattatcatctaccgagctgcctacttcggtatctatgacaccgcaaaggga
atgcttccagatcccaagaatactcacatcttcatcagctggatgatcgcacaatccgtc
acagcggttgccgggctgacttcctacccgtttgacactgttcgccgccgaatgatgatg
cagtcagggcgcaaaggaaccgatatcatgtacacgggcacaatagactgctggaggaag
attgctcgggatgaaggaggcaaggcgtttttcaagggggcgtggtccaatgttctccga
ggcatgggtggtgcttttgtgctggtcttgtatgatgaaatcaagaagttcacataa
DBGET
integrated database retrieval system
