Mastomys coucha (southern multimammate mouse): 116099029
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Entry
116099029 CDS
T07224
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
KO
K05862
voltage-dependent anion channel protein 1
Organism
mcoc
Mastomys coucha (southern multimammate mouse)
Pathway
mcoc04020
Calcium signaling pathway
mcoc04022
cGMP-PKG signaling pathway
mcoc04217
Necroptosis
mcoc04218
Cellular senescence
mcoc04613
Neutrophil extracellular trap formation
mcoc04621
NOD-like receptor signaling pathway
mcoc04979
Cholesterol metabolism
mcoc05010
Alzheimer disease
mcoc05012
Parkinson disease
mcoc05014
Amyotrophic lateral sclerosis
mcoc05016
Huntington disease
mcoc05017
Spinocerebellar ataxia
mcoc05020
Prion disease
mcoc05022
Pathways of neurodegeneration - multiple diseases
mcoc05164
Influenza A
mcoc05166
Human T-cell leukemia virus 1 infection
mcoc05208
Chemical carcinogenesis - reactive oxygen species
mcoc05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
mcoc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
116099029
04022 cGMP-PKG signaling pathway
116099029
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
116099029
04218 Cellular senescence
116099029
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
116099029
04621 NOD-like receptor signaling pathway
116099029
09154 Digestive system
04979 Cholesterol metabolism
116099029
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
116099029
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
116099029
05164 Influenza A
116099029
09164 Neurodegenerative disease
05010 Alzheimer disease
116099029
05012 Parkinson disease
116099029
05014 Amyotrophic lateral sclerosis
116099029
05016 Huntington disease
116099029
05017 Spinocerebellar ataxia
116099029
05020 Prion disease
116099029
05022 Pathways of neurodegeneration - multiple diseases
116099029
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
116099029
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
mcoc03029
]
116099029
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
mcoc04040
]
116099029
Mitochondrial biogenesis [BR:
mcoc03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
116099029
Ion channels [BR:
mcoc04040
]
Chloride channels
Maxi chloride channel (VDAC)
116099029
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
116099029
NCBI-ProteinID:
XP_031237965
LinkDB
All DBs
Position
Unknown
AA seq
283 aa
AA seq
DB search
MAVPPTYADLGKSARDVFSKGYGFGLIKLDLKMKSENGLEFTSSGSANTETTKVNGSLET
KYRWTEYGLTFTEXXXXXXXXGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETSKSRVTQSNFAVDYKTDEFQL
HTNVNDGTEFGGSIYQKVKKKLETAVNLAWTAGNSNTRFGIAAKYQVDPDACFSAKENNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNVGGHKLGLGLEFQA
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atggctgtgcctccaacatacgctgatcttggcaagtccgccagggatgttttctccaag
ggctatggctttggcttaataaaacttgatttgaaaatgaagtcggagaatgggttggaa
tttaccagctcaggctctgccaacacggaaactaccaaagtgaatggcagtctggaaacc
aagtacagatggactgagtatgggctaacatttacagagnnnnnnnnnnnnnnnnnnnnn
nnnggcactgagatcactgtggaagaccagcttgctcgtggactgaagctgacctttgat
tcatctttctcacctaacactgggaaaaaaaatgctaaaatcaagacagggtacaagagg
gagcatatcaacctgggctgtgacgtggactttgacatcgctgggccctcaatccggggt
gctctggtgcttggctatgagggttggctggctggctaccagatgaattttgagacctcg
aagtcccgagtgacccagagcaactttgcagttgactataagacggacgaattccagctt
catactaatgtgaatgacgggacagagtttggtggctccatttaccagaaggtgaaaaag
aagttggagactgccgtcaatcttgcctggactgcaggaaacagtaacactcgctttgga
atagcagccaaatatcaggtcgaccctgatgcctgcttttcggccaaagagaacaactcc
agcctgattggcttagggtacacccagactctaaaaccaggtatcaaactgacgctgtca
gccctgctggatggcaagaacgtcaatgtgggcggccacaagcttggtctaggactggaa
tttcaagcataa
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