Neogale vison (American mink): 122902898
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Entry
122902898 CDS
T08764
Symbol
SMAD2
Name
(RefSeq) mothers against decapentaplegic homolog 2 isoform X1
KO
K04500
mothers against decapentaplegic homolog 2
Organism
nvs
Neogale vison (American mink)
Pathway
nvs04110
Cell cycle
nvs04144
Endocytosis
nvs04218
Cellular senescence
nvs04350
TGF-beta signaling pathway
nvs04371
Apelin signaling pathway
nvs04390
Hippo signaling pathway
nvs04550
Signaling pathways regulating pluripotency of stem cells
nvs04659
Th17 cell differentiation
nvs04926
Relaxin signaling pathway
nvs04933
AGE-RAGE signaling pathway in diabetic complications
nvs05142
Chagas disease
nvs05166
Human T-cell leukemia virus 1 infection
nvs05200
Pathways in cancer
nvs05205
Proteoglycans in cancer
nvs05210
Colorectal cancer
nvs05212
Pancreatic cancer
nvs05225
Hepatocellular carcinoma
nvs05226
Gastric cancer
nvs05321
Inflammatory bowel disease
nvs05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09130 Environmental Information Processing
09132 Signal transduction
04350 TGF-beta signaling pathway
122902898 (SMAD2)
04390 Hippo signaling pathway
122902898 (SMAD2)
04371 Apelin signaling pathway
122902898 (SMAD2)
09140 Cellular Processes
09141 Transport and catabolism
04144 Endocytosis
122902898 (SMAD2)
09143 Cell growth and death
04110 Cell cycle
122902898 (SMAD2)
04218 Cellular senescence
122902898 (SMAD2)
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
122902898 (SMAD2)
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
122902898 (SMAD2)
09152 Endocrine system
04926 Relaxin signaling pathway
122902898 (SMAD2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
122902898 (SMAD2)
05205 Proteoglycans in cancer
122902898 (SMAD2)
09162 Cancer: specific types
05210 Colorectal cancer
122902898 (SMAD2)
05212 Pancreatic cancer
122902898 (SMAD2)
05225 Hepatocellular carcinoma
122902898 (SMAD2)
05226 Gastric cancer
122902898 (SMAD2)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
122902898 (SMAD2)
09174 Infectious disease: parasitic
05142 Chagas disease
122902898 (SMAD2)
09163 Immune disease
05321 Inflammatory bowel disease
122902898 (SMAD2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
122902898 (SMAD2)
09167 Endocrine and metabolic disease
04933 AGE-RAGE signaling pathway in diabetic complications
122902898 (SMAD2)
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GFIT
Motif
Pfam:
MH2
MH1
IRF-3
Motif
Other DBs
NCBI-GeneID:
122902898
NCBI-ProteinID:
XP_044098964
LinkDB
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Position
3:149558135..149633399
Genome browser
AA seq
467 aa
AA seq
DB search
MSSILPFTPPVVKRLLGWKKSAGGSGGAGGGEQNGQEEKWCEKAVKSLVKKLKKTGRLDE
LEKAITTQNCNTKCVTIPSTCSEIWGLSTPNTIDQWDTTGLYSFSEQTRSLDGRLQVSHR
KGLPHVIYCRLWRWPDLHSHHELKAIENCEYAFNLKKDEVCVNPYHYQRVETPVLPPVLV
PRHTEILTELPPLDDYTHSIPENTNFPAGIEPQSNYIPETPPPGYISEDGETSDQQLNQS
MDTGSPAELSPTTLSPVNHSLDLQPVTYSEPAFWCSIAYYELNQRVGETFHASQPSLTVD
GFTDPSNSERFCLGLLSNVNRNATVEMTRRHIGRGVRLYYIGGEVFAECLSDSAIFVQSP
NCNQRYGWHPATVCKIPPGCNLKIFNNQEFAALLAQSVNQGFEAVYQLTRMCTIRMSFVK
GWGAEYRRQTVTSTPCWIELHLNGPLQWLDKVLTQMGSPSVRCSSMS
NT seq
1404 nt
NT seq
+upstream
nt +downstream
nt
atgtcgtccatcttgccattcactccaccagttgtgaaaaggctgctgggatggaagaaa
tcagctggtggatctggaggagcaggcggaggagagcagaatggacaagaagaaaagtgg
tgtgagaaagcagttaaaagtttggtgaagaaactaaagaaaacaggacgattagatgag
cttgagaaagccatcaccactcaaaattgtaatactaaatgtgtcaccataccaagcact
tgctctgaaatttggggactgagtacaccaaatacgatagatcagtgggatacaacaggc
ctttacagcttctctgaacaaaccaggtctctggatggccgtctacaagtgtcccatcgg
aaaggactgccacacgtgatatattgccgattgtggcgctggcctgaccttcacagtcac
catgagctcaaagcaattgaaaactgcgaatatgcttttaatcttaaaaaggatgaagta
tgtgtaaacccttaccactaccagagagttgagacaccagttctgcctcccgtactggtg
ccgcggcacactgagatcctaacagagctgcctcctctggacgattatacccactccatt
ccagaaaacactaatttcccagcaggaattgagccacagagtaattacatcccagaaacg
ccacctcctggatatatcagtgaggatggagaaacaagcgatcagcagttgaaccaaagt
atggatacaggatctccagcagaactatctcctactactctttcccccgttaatcatagt
ttggatttgcagccagttacttactcagaacctgcattttggtgttcaatagcctattat
gaattaaaccagagggttggcgagaccttccacgcatcacagccctcactcactgtcgac
ggtttcacagatccatccaattcagagaggttctgcctagggttgctctccaacgtcaac
cgaaacgcgactgtagaaatgacaagaagacatataggaagaggagtgcgcttatattac
atcggtggagaagtttttgccgagtgcctaagtgatagtgcaatctttgtgcagagcccc
aactgtaatcagagatacggctggcaccctgcaaccgtgtgtaaaatcccgccaggctgt
aatctgaagatcttcaacaaccaggaatttgctgctcttctggctcagtccgttaatcag
ggttttgaagccgtgtatcagctaactagaatgtgcaccataagaatgagttttgtgaaa
gggtggggagcagaataccgaaggcagacggtaacgagcactccttgctggattgagctt
catctgaatggacctctacagtggttggacaaagtattaactcagatgggatccccttca
gtgcgttgctcgagcatgtcataa
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