Neogale vison (American mink): 122911145
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Entry
122911145 CDS
T08764
Name
(RefSeq) cytochrome b-245 light chain
KO
K08009
cytochrome b-245, alpha polypeptide
Organism
nvs
Neogale vison (American mink)
Pathway
nvs04145
Phagosome
nvs04380
Osteoclast differentiation
nvs04613
Neutrophil extracellular trap formation
nvs04621
NOD-like receptor signaling pathway
nvs04670
Leukocyte transendothelial migration
nvs05020
Prion disease
nvs05140
Leishmaniasis
nvs05208
Chemical carcinogenesis - reactive oxygen species
nvs05415
Diabetic cardiomyopathy
nvs05417
Lipid and atherosclerosis
nvs05418
Fluid shear stress and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09140 Cellular Processes
09141 Transport and catabolism
04145 Phagosome
122911145
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
122911145
04621 NOD-like receptor signaling pathway
122911145
04670 Leukocyte transendothelial migration
122911145
09158 Development and regeneration
04380 Osteoclast differentiation
122911145
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
122911145
09174 Infectious disease: parasitic
05140 Leishmaniasis
122911145
09164 Neurodegenerative disease
05020 Prion disease
122911145
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
122911145
05418 Fluid shear stress and atherosclerosis
122911145
05415 Diabetic cardiomyopathy
122911145
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
nvs04131
]
122911145
Membrane trafficking [BR:
nvs04131
]
Others
NADPH oxidases (Nox) and associated proteins
Nox associated proteins
122911145
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Paralog
Gene cluster
GFIT
Motif
Pfam:
Cytochrom_B558a
Cg6151-P
Motif
Other DBs
NCBI-GeneID:
122911145
NCBI-ProteinID:
XP_044111505
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All DBs
Position
7:1045885..1053354
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AA seq
194 aa
AA seq
DB search
MGQIEWAMWANEQALASGLILIMGGVVATAGQFTKWYFGAYSIGAGVFVCLLEYPRGKRR
KGSTMERCGQKYMTKVLKVFGPLTRNYYIRAFLHLGLSVPAGFLLATILGMACLAIASSI
YLLAAVRGEQWVPIEPKPKERPQVGGTIKQPPSNPPPRPPAEARKKPGEEEAAGVAGVSG
GPQENPVPVIDEVV
NT seq
585 nt
NT seq
+upstream
nt +downstream
nt
atggggcagatcgagtgggccatgtgggccaacgaacaggcgctggcgtccggcctgatc
ctcatcatggggggcgtcgtggccacggccggccagttcaccaagtggtacttcggcgcg
tactccattggcgcaggcgtgttcgtctgcctgctggagtacccccgggggaagaggagg
aagggatccaccatggagagatgtggacagaagtacatgaccaaagtgctgaaggtgttc
gggcctctcaccaggaactactacatccgggccttcctgcacctggggctgtcggtacct
gccggcttcctgcttgccaccatcctggggatggcctgcctggccatcgcgagcagcatc
tatctgctggcggccgtccggggagagcagtgggtccccatcgagcccaagcccaaggag
cggccgcaagtcgggggcaccatcaagcagccgcccagcaaccccccgccccggccccca
gccgaggcccgaaagaagcctggggaagaggaggcagcaggggtggcaggggtttccggt
ggcccccaggaaaacccggtcccggtgatcgacgaggtcgtgtga
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