Mustela nigripes (black-footed ferret): 132020469
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Entry
132020469 CDS
T09425
Symbol
NCF4
Name
(RefSeq) neutrophil cytosol factor 4 isoform X1
KO
K08012
neutrophil cytosolic factor 4
Organism
mnp
Mustela nigripes (black-footed ferret)
Pathway
mnp04145
Phagosome
mnp04380
Osteoclast differentiation
mnp04613
Neutrophil extracellular trap formation
mnp04670
Leukocyte transendothelial migration
mnp05020
Prion disease
mnp05140
Leishmaniasis
mnp05415
Diabetic cardiomyopathy
mnp05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
mnp00001
]
09140 Cellular Processes
09141 Transport and catabolism
04145 Phagosome
132020469 (NCF4)
09150 Organismal Systems
09151 Immune system
04613 Neutrophil extracellular trap formation
132020469 (NCF4)
04670 Leukocyte transendothelial migration
132020469 (NCF4)
09158 Development and regeneration
04380 Osteoclast differentiation
132020469 (NCF4)
09160 Human Diseases
09174 Infectious disease: parasitic
05140 Leishmaniasis
132020469 (NCF4)
09164 Neurodegenerative disease
05020 Prion disease
132020469 (NCF4)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
132020469 (NCF4)
05415 Diabetic cardiomyopathy
132020469 (NCF4)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
mnp04131
]
132020469 (NCF4)
Membrane trafficking [BR:
mnp04131
]
Others
NADPH oxidases (Nox) and associated proteins
Nox associated proteins
132020469 (NCF4)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PX
SH3_9
SH3_1
PB1
SH3_2
Motif
Other DBs
NCBI-GeneID:
132020469
NCBI-ProteinID:
XP_059260595
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All DBs
Position
6:complement(10848791..10864868)
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AA seq
339 aa
AA seq
DB search
MALAQQLRAESDFEQLPDDVAISANIADIEEKRGFTSYFVFVIEVKTKGGSKYLIYRRYR
QFYALQSKLEERFGPENKTSPFTCSLPTLPAKVYMGVKQEIAEMRIPALNAYMKSLLSLP
IWVLMDEDVRIFFYQSPYDSEQVPQALRRLRPRTRKIKSESPQGAIIDRMAAPRAEALFD
FTGNSKLELNFKVGDVIFLLSRINKDWLEGTVRGATGIFPQSFVKILKDFPEEEDPTNWL
RCYYYEDTISTTKDIAVDEDLSSTPLFKDLLQLMRREFQREDIALNYRDTEGDLVRLLSD
EDVVLMVRQAQGLPSQKRLFPWKLHITQKDDYAVYNTVP
NT seq
1020 nt
NT seq
+upstream
nt +downstream
nt
atggccctggcccagcagctgcgagccgagagtgactttgagcagcttcccgacgacgtc
gccatctccgccaacatcgctgacatcgaggagaaaaggggcttcaccagctactttgtg
ttcgtcatcgaggtgaagacaaaagggggctcaaaatacctcatctaccgtcgctaccgc
cagttctatgccctgcagagcaagctggaggagcggtttgggccggagaacaagaccagc
ccgttcacctgcagcttgcccacgctcccagccaaagtctacatgggtgtgaaacaggag
atcgcggagatgcggattcctgccctcaacgcctacatgaagagcctcctcagcctaccc
atctgggtgctgatggacgaggatgtccggatcttcttctaccagtcgccctatgattca
gagcaggtgccccaggccctgcgccggctccggccacgcacccggaaaatcaagagcgag
tccccacaaggcgccatcattgaccgcatggcagctccgcgagcggaggccctgtttgac
ttcacgggcaacagcaaactggaactgaatttcaaagtcggagatgtgatcttccttctc
agccggatcaataaagactggctggagggcactgtgaggggagccacgggcatcttccca
cagtcgttcgtgaaaatcctcaaggacttcccggaggaagaagaccctaccaactggctg
cgctgctactactacgaggacaccatcagcaccaccaaggacatcgcagtggacgaggac
ctcagcagcactccactgttcaaggacctgctgcagctcatgaggcgggagttccagagg
gaagacatcgccctaaattaccgggacaccgagggcgatctggtgaggctgctctcagac
gaggacgtggtgctcatggtgaggcaggcccagggtctcccctcccagaaacgcctcttc
ccctggaagctgcatatcacccagaaggatgactacgcggtctacaacactgtcccctga
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