Bos mutus (wild yak): 102280707
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Entry
102280707 CDS
T02919
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3
KO
K15041
voltage-dependent anion channel protein 3
Organism
bom
Bos mutus (wild yak)
Pathway
bom04020
Calcium signaling pathway
bom04022
cGMP-PKG signaling pathway
bom04216
Ferroptosis
bom04217
Necroptosis
bom04218
Cellular senescence
bom04613
Neutrophil extracellular trap formation
bom04621
NOD-like receptor signaling pathway
bom04979
Cholesterol metabolism
bom05010
Alzheimer disease
bom05012
Parkinson disease
bom05016
Huntington disease
bom05017
Spinocerebellar ataxia
bom05020
Prion disease
bom05022
Pathways of neurodegeneration - multiple diseases
bom05161
Hepatitis B
bom05166
Human T-cell leukemia virus 1 infection
bom05203
Viral carcinogenesis
bom05208
Chemical carcinogenesis - reactive oxygen species
bom05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
bom00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
102280707 (VDAC3)
04022 cGMP-PKG signaling pathway
102280707 (VDAC3)
09140 Cellular Processes
09143 Cell growth and death
04216 Ferroptosis
102280707 (VDAC3)
04217 Necroptosis
102280707 (VDAC3)
04218 Cellular senescence
102280707 (VDAC3)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
102280707 (VDAC3)
04621 NOD-like receptor signaling pathway
102280707 (VDAC3)
09154 Digestive system
04979 Cholesterol metabolism
102280707 (VDAC3)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
102280707 (VDAC3)
05203 Viral carcinogenesis
102280707 (VDAC3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
102280707 (VDAC3)
05161 Hepatitis B
102280707 (VDAC3)
09164 Neurodegenerative disease
05010 Alzheimer disease
102280707 (VDAC3)
05012 Parkinson disease
102280707 (VDAC3)
05016 Huntington disease
102280707 (VDAC3)
05017 Spinocerebellar ataxia
102280707 (VDAC3)
05020 Prion disease
102280707 (VDAC3)
05022 Pathways of neurodegeneration - multiple diseases
102280707 (VDAC3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
102280707 (VDAC3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
bom03029
]
102280707 (VDAC3)
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
bom04040
]
102280707 (VDAC3)
Mitochondrial biogenesis [BR:
bom03029
]
Mitochondrial protein import machinery
Outer membrane
Porin
102280707 (VDAC3)
Ion channels [BR:
bom04040
]
Chloride channels
Maxi chloride channel (VDAC)
102280707 (VDAC3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Porin_3
Motif
Other DBs
NCBI-GeneID:
102280707
NCBI-ProteinID:
XP_070220303
LinkDB
All DBs
Position
27:complement(8329721..8341786)
Genome browser
AA seq
283 aa
AA seq
DB search
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVEFSTSGHAYTDTGKASGNLET
KYKICNYGLTFTQKWNTDNTLGTEISWENKLAEGLKLTLDTIFVPNTGKKSGKLKASYKR
DCFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQL
HTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNNA
SLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq
852 nt
NT seq
+upstream
nt +downstream
nt
atgtgtaacacaccgacttactgtgacctaggaaaggctgccaaagatgtcttcaacaaa
ggatatggatttggcatggtcaaaatagatctgagaaccaagtcatgtagtggagtggaa
ttttctacttctggtcatgcttacactgatacagggaaagcatcaggcaacctagagacc
aaatacaagatctgtaactatggactgaccttcacgcagaagtggaacacagacaatact
cttgggacagaaatctcttgggagaataagttggctgaagggttgaaactgactcttgat
accatatttgtaccgaacacaggaaagaagagtgggaaattgaaggcctcatataaacgg
gattgtttcagtcttggcagtaatgttgatatagatttttcaggaccaaccatctatggc
tgggctgtgttggcctttgaaggttggcttgctggctatcagatgagttttgacacagcc
aaatccaaactgtcacagaataatttcgccctgggttacaaggccgcagacttccagctg
cacactcatgtgaatgatggcactgagtttggagggtccatctaccagaaggtgaatgag
aagattgaaacgtcaataaacctcgcgtggacagctggcagtaacaacacccgcttcggc
atcgctgctaagtacaagctggactgcagaacttctctctctgctaaagtaaacaatgcc
agcctgattggactgggttacactcagacccttcgaccaggagtgaaactgaccctgtca
gctctaattgatggaaagaacttcaatgcaggagggcacaaggtcggtctgggatttgaa
ctagaagcttaa
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