Neogale vison (American mink): 122916938
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Entry
122916938 CDS
T08764
Symbol
IFNB1
Name
(RefSeq) interferon beta
KO
K05415
interferon beta
Organism
nvs
Neogale vison (American mink)
Pathway
nvs04060
Cytokine-cytokine receptor interaction
nvs04151
PI3K-Akt signaling pathway
nvs04217
Necroptosis
nvs04380
Osteoclast differentiation
nvs04620
Toll-like receptor signaling pathway
nvs04621
NOD-like receptor signaling pathway
nvs04622
RIG-I-like receptor signaling pathway
nvs04623
Cytosolic DNA-sensing pathway
nvs04630
JAK-STAT signaling pathway
nvs04650
Natural killer cell mediated cytotoxicity
nvs04668
TNF signaling pathway
nvs04936
Alcoholic liver disease
nvs05135
Yersinia infection
nvs05142
Chagas disease
nvs05152
Tuberculosis
nvs05160
Hepatitis C
nvs05161
Hepatitis B
nvs05162
Measles
nvs05163
Human cytomegalovirus infection
nvs05164
Influenza A
nvs05165
Human papillomavirus infection
nvs05167
Kaposi sarcoma-associated herpesvirus infection
nvs05168
Herpes simplex virus 1 infection
nvs05169
Epstein-Barr virus infection
nvs05170
Human immunodeficiency virus 1 infection
nvs05171
Coronavirus disease - COVID-19
nvs05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09130 Environmental Information Processing
09132 Signal transduction
04630 JAK-STAT signaling pathway
122916938 (IFNB1)
04668 TNF signaling pathway
122916938 (IFNB1)
04151 PI3K-Akt signaling pathway
122916938 (IFNB1)
09133 Signaling molecules and interaction
04060 Cytokine-cytokine receptor interaction
122916938 (IFNB1)
09140 Cellular Processes
09143 Cell growth and death
04217 Necroptosis
122916938 (IFNB1)
09150 Organismal Systems
09151 Immune system
04620 Toll-like receptor signaling pathway
122916938 (IFNB1)
04621 NOD-like receptor signaling pathway
122916938 (IFNB1)
04622 RIG-I-like receptor signaling pathway
122916938 (IFNB1)
04623 Cytosolic DNA-sensing pathway
122916938 (IFNB1)
04650 Natural killer cell mediated cytotoxicity
122916938 (IFNB1)
09158 Development and regeneration
04380 Osteoclast differentiation
122916938 (IFNB1)
09160 Human Diseases
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
122916938 (IFNB1)
05161 Hepatitis B
122916938 (IFNB1)
05160 Hepatitis C
122916938 (IFNB1)
05171 Coronavirus disease - COVID-19
122916938 (IFNB1)
05164 Influenza A
122916938 (IFNB1)
05162 Measles
122916938 (IFNB1)
05168 Herpes simplex virus 1 infection
122916938 (IFNB1)
05163 Human cytomegalovirus infection
122916938 (IFNB1)
05167 Kaposi sarcoma-associated herpesvirus infection
122916938 (IFNB1)
05169 Epstein-Barr virus infection
122916938 (IFNB1)
05165 Human papillomavirus infection
122916938 (IFNB1)
09171 Infectious disease: bacterial
05135 Yersinia infection
122916938 (IFNB1)
05152 Tuberculosis
122916938 (IFNB1)
09174 Infectious disease: parasitic
05142 Chagas disease
122916938 (IFNB1)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
122916938 (IFNB1)
09167 Endocrine and metabolic disease
04936 Alcoholic liver disease
122916938 (IFNB1)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04052 Cytokines and neuropeptides [BR:
nvs04052
]
122916938 (IFNB1)
Cytokines and neuropeptides [BR:
nvs04052
]
Cytokines
Interferons
122916938 (IFNB1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Interferon
Motif
Other DBs
NCBI-GeneID:
122916938
NCBI-ProteinID:
XP_044120260
UniProt:
A0A8C7AYN9
LinkDB
All DBs
Position
9:47874063..47874623
Genome browser
AA seq
186 aa
AA seq
DB search
MTSRYILQTALLVYFSTTVLAMNYNLLRFQLSSSSVECQELLLQLNGTSKDCLKDRMNFK
IPEEIQKSQKFQKEDIVLVTLEMFQKTSDIFRRNLSSMGWNESIVENLLATLHWQKEHLE
EILEDIMQEENFTWDHRTLLHLKRYYLRIVRYLKAKEFSVCAWTIVQAEILKSFFFLDKL
IDSLPN
NT seq
561 nt
NT seq
+upstream
nt +downstream
nt
atgaccagcaggtatatcctccaaactgctctcctggtatatttctccaccacggttctt
gccatgaactataacttacttcgattccaactaagcagcagcagtgtggagtgccaggag
ctccttctacagctgaatggaacttctaaagattgcctcaaggacaggatgaacttcaag
atccctgaggagatccagaaatcccagaagttccagaaggaggacatcgtattggtcacc
cttgagatgttccagaagacctctgatattttcaggagaaatctctcaagcatgggatgg
aatgagagcattgtcgagaacctccttgccacactccactggcagaaggaacatctggag
gaaatcctggaggacatcatgcaggaggaaaacttcacttgggaccacaggacccttctg
cacctgaagagatattatctaaggatcgtgcggtacctgaaagccaaggagttcagcgtc
tgtgcctggacaatagtgcaagcagaaatcctcaagagctttttcttccttgataaactt
atagattctctccctaactga
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