Rhinopithecus roxellana (golden snub-nosed monkey): 104666042
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Entry
104666042 CDS
T03989
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
KO
K15041
voltage-dependent anion channel protein 3
Organism
rro
Rhinopithecus roxellana (golden snub-nosed monkey)
Pathway
rro04020
Calcium signaling pathway
rro04022
cGMP-PKG signaling pathway
rro04216
Ferroptosis
rro04217
Necroptosis
rro04218
Cellular senescence
rro04613
Neutrophil extracellular trap formation
rro04621
NOD-like receptor signaling pathway
rro04979
Cholesterol metabolism
rro05010
Alzheimer disease
rro05012
Parkinson disease
rro05016
Huntington disease
rro05017
Spinocerebellar ataxia
rro05020
Prion disease
rro05022
Pathways of neurodegeneration - multiple diseases
rro05161
Hepatitis B
rro05166
Human T-cell leukemia virus 1 infection
rro05203
Viral carcinogenesis
rro05208
Chemical carcinogenesis - reactive oxygen species
rro05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
rro00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
104666042 (VDAC3)
04022 cGMP-PKG signaling pathway
104666042 (VDAC3)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
104666042 (VDAC3)
04217 Necroptosis
104666042 (VDAC3)
04218 Cellular senescence
104666042 (VDAC3)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
104666042 (VDAC3)
04621 NOD-like receptor signaling pathway
104666042 (VDAC3)
09154 Digestive system
04979 Cholesterol metabolism
104666042 (VDAC3)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
104666042 (VDAC3)
05203 Viral carcinogenesis
104666042 (VDAC3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
104666042 (VDAC3)
05161 Hepatitis B
104666042 (VDAC3)
09164 Neurodegenerative disease
05010 Alzheimer disease
104666042 (VDAC3)
05012 Parkinson disease
104666042 (VDAC3)
05016 Huntington disease
104666042 (VDAC3)
05017 Spinocerebellar ataxia
104666042 (VDAC3)
05020 Prion disease
104666042 (VDAC3)
05022 Pathways of neurodegeneration - multiple diseases
104666042 (VDAC3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
104666042 (VDAC3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
rro03029
]
104666042 (VDAC3)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
rro04040
]
104666042 (VDAC3)
Mitochondrial biogenesis [BR:
rro03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
104666042 (VDAC3)
Ion channels [BR:
rro04040
]
Chloride channels
Maxi chloride channel (VDAC)
104666042 (VDAC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
104666042
NCBI-ProteinID:
XP_010366332
UniProt:
A0A2K6RKL5
LinkDB
All DBs
Position
9:complement(7265219..7280047)
Genome browser
AA seq
284 aa
AA seq
DB search
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLKTKSCSGVMEFSTSGHAYTDTGKASGNLE
TKYKVCNYGLTFTQKWNTDNTLGTEISWENKLAEGLKLTLDTIFVPNTGKKSGKLKASYK
RDCFSVGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQ
LHTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNN
ASLIGLGYTQTLRPGVKLTLSALIDGKNFSAGGHKVGLGFELEA
NT seq
855 nt
NT seq
+upstream
nt +downstream
nt
atgtgtaacacaccaacttactgtgacctaggaaaggctgctaaggatgtcttcaacaaa
ggatatggctttggcatggtcaagatagacctgaaaaccaagtcttgtagcggagtgatg
gaattttctacttctggtcatgcttacactgatacagggaaagcatcaggcaacctagaa
accaaatataaggtctgtaactatggacttaccttcacccaaaaatggaacacggacaat
actctagggacagaaatctcttgggagaataagttggctgaagggttgaaactgactctt
gataccatatttgtaccgaacacaggaaagaagagtgggaaattgaaggcctcctataaa
cgggattgttttagtgttggcagtaatgttgatatagatttttctggaccaaccatctat
ggctgggctgtgttggctttcgaagggtggcttgctggctatcagatgagttttgacaca
gccaaatccaaactgtcacagaataatttcgccctgggttacaaggctgcggacttccag
ctgcacacacatgtgaacgacggcactgagttcggaggttctatctaccagaaggttaat
gagaagattgaaacatccataaaccttgcttggacggctgggagtaacaacacccgtttt
ggcattgctgctaagtacaagctggattgtagaacttctctctctgctaaagtaaataat
gccagcctgattggactgggttatactcagacccttcgaccaggagtcaaattgacttta
tcagctttaatcgatgggaagaacttcagtgcaggaggtcacaaggttggcttgggattt
gaactggaagcttaa
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