Eulemur rufifrons (Bennett's brown lemur): 138392131
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Entry
138392131 CDS
T11398
Symbol
SMAD3
Name
(RefSeq) mothers against decapentaplegic homolog 3 isoform X1
KO
K23605
mothers against decapentaplegic homolog 3
Organism
eruf Eulemur rufifrons (Bennett's brown lemur)
Pathway
eruf04068
FoxO signaling pathway
eruf04110
Cell cycle
eruf04144
Endocytosis
eruf04218
Cellular senescence
eruf04310
Wnt signaling pathway
eruf04350
TGF-beta signaling pathway
eruf04371
Apelin signaling pathway
eruf04390
Hippo signaling pathway
eruf04520
Adherens junction
eruf04550
Signaling pathways regulating pluripotency of stem cells
eruf04659
Th17 cell differentiation
eruf04933
AGE-RAGE signaling pathway in diabetic complications
eruf05161
Hepatitis B
eruf05166
Human T-cell leukemia virus 1 infection
eruf05200
Pathways in cancer
eruf05210
Colorectal cancer
eruf05212
Pancreatic cancer
eruf05220
Chronic myeloid leukemia
eruf05225
Hepatocellular carcinoma
eruf05226
Gastric cancer
eruf05321
Inflammatory bowel disease
eruf05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
eruf00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
138392131 (SMAD3)
04350 TGF-beta signaling pathway
138392131 (SMAD3)
04390 Hippo signaling pathway
138392131 (SMAD3)
04371 Apelin signaling pathway
138392131 (SMAD3)
04068 FoxO signaling pathway
138392131 (SMAD3)
09140 Cellular Processes
09141 Transport and catabolism
04144 Endocytosis
138392131 (SMAD3)
09143 Cell growth and death
04110 Cell cycle
138392131 (SMAD3)
04218 Cellular senescence
138392131 (SMAD3)
09144 Cellular community - eukaryotes
04520 Adherens junction
138392131 (SMAD3)
04550 Signaling pathways regulating pluripotency of stem cells
138392131 (SMAD3)
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
138392131 (SMAD3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
138392131 (SMAD3)
09162 Cancer: specific types
05210 Colorectal cancer
138392131 (SMAD3)
05212 Pancreatic cancer
138392131 (SMAD3)
05225 Hepatocellular carcinoma
138392131 (SMAD3)
05226 Gastric cancer
138392131 (SMAD3)
05220 Chronic myeloid leukemia
138392131 (SMAD3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
138392131 (SMAD3)
05161 Hepatitis B
138392131 (SMAD3)
09163 Immune disease
05321 Inflammatory bowel disease
138392131 (SMAD3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
138392131 (SMAD3)
09167 Endocrine and metabolic disease
04933 AGE-RAGE signaling pathway in diabetic complications
138392131 (SMAD3)
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NCBI-GeneID:
138392131
NCBI-ProteinID:
XP_069338633
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Position
2:complement(28674312..28788439)
Genome browser
AA seq
425 aa
AA seq
DB search
MSSILPFTPPIVKRLLGWKKGEQNGQEEKWCEKAVKSLVKKLKKTGQLDELEKAITTQNV
NTKCITIPRSLDGRLQVSHRKGLPHVIYCRLWRWPDLHSHHELRAMELCEFAFNMKKDEV
CVNPYHYQRVETPVLPPVLVPRHTEIPAEFPPLDDYSHSIPENTNFPAGIEPQSNIPETP
PPGYLSEDGETSDHQMNHSMDAGSPNLSPNPMSPAHNNLDLQPVTYCEPAFWCSISYYEL
NQRVGETFHASQPSMTVDGFTDPSNSERFCLGLLSNVNRNAAVELTRRHIGRGVRLYYIG
GEVFAECLSDSAIFVQSPNCNQRYGWHPATVCKIPPGCNLKIFNNQEFAALLAQSVNQGF
EAVYQLTRMCTIRMSFVKGWGAEYRRQTVTSTPCWIELHLNGPLQWLDKVLTQMGSPSIR
CSSVS
NT seq
1278 nt
NT seq
+upstream
nt +downstream
nt
atgtcgtccatcctgcccttcacccccccgattgtgaagcgcttgctgggctggaagaag
ggcgagcagaacgggcaggaagagaagtggtgtgagaaggcagtcaagagcttggtcaag
aagctcaagaagacggggcagctggacgagctggagaaggccatcaccacgcagaacgtc
aacaccaagtgcatcactatccccaggtccctggacggccggctgcaggtgtcccatcgg
aaggggctcccccatgtcatctactgccgcctgtggcggtggcccgacctgcacagccac
catgagctgcgggccatggagctgtgtgagttcgccttcaacatgaagaaggacgaggtc
tgtgtgaatccctaccactaccagagagtagagacgccagttctacctcctgtgttggtg
ccacgccacacagagatcccggccgagttccccccgctggacgactacagccattccatc
cccgaaaacactaacttccctgcgggcatcgagccccagagcaatattccagagacccca
ccccctggctacctgagtgaagatggagaaaccagcgaccaccagatgaaccacagcatg
gacgcaggttctccaaacctatccccgaatccgatgtccccagcacacaataacttggac
ctgcagcctgtcacctactgcgagccggccttctggtgctccatctcctactacgagctg
aaccagcgtgtcggggagacattccacgcctcgcagccgtccatgacggtggacggcttc
accgacccctccaactcggagcgcttctgcctggggctgctctccaacgtcaacaggaac
gcagcagtggagctcactcggaggcacatcgggagaggtgtgcggctctactacattgga
ggggaggtctttgcagagtgcctcagcgacagcgctatttttgtccagtctcccaactgt
aaccagcgctatggctggcacccagccaccgtctgcaagatcccaccagggtgcaacctg
aagatcttcaacaatcaggagttcgccgccctcctggcgcagtccgtcaaccagggcttc
gaggccgtctaccagctgactcggatgtgcaccatccgcatgagcttcgtcaaaggctgg
ggcgcggaatacaggagacagacagtgaccagcaccccctgctggattgagctgcacctg
aatgggcctttgcagtggctcgacaaggtcctcacccagatgggctccccaagcatccgc
tgttccagcgtgtcttag
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