Panthera tigris altaica (Amur tiger): 102971888
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Entry
102971888 CDS
T02988
Symbol
SMAD3
Name
(RefSeq) SMAD family member 3
KO
K23605
mothers against decapentaplegic homolog 3
Organism
ptg
Panthera tigris altaica (Amur tiger)
Pathway
ptg04068
FoxO signaling pathway
ptg04110
Cell cycle
ptg04144
Endocytosis
ptg04218
Cellular senescence
ptg04310
Wnt signaling pathway
ptg04350
TGF-beta signaling pathway
ptg04371
Apelin signaling pathway
ptg04390
Hippo signaling pathway
ptg04520
Adherens junction
ptg04550
Signaling pathways regulating pluripotency of stem cells
ptg04659
Th17 cell differentiation
ptg04933
AGE-RAGE signaling pathway in diabetic complications
ptg05161
Hepatitis B
ptg05166
Human T-cell leukemia virus 1 infection
ptg05200
Pathways in cancer
ptg05210
Colorectal cancer
ptg05212
Pancreatic cancer
ptg05220
Chronic myeloid leukemia
ptg05225
Hepatocellular carcinoma
ptg05226
Gastric cancer
ptg05321
Inflammatory bowel disease
ptg05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
ptg00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
102971888 (SMAD3)
04350 TGF-beta signaling pathway
102971888 (SMAD3)
04390 Hippo signaling pathway
102971888 (SMAD3)
04371 Apelin signaling pathway
102971888 (SMAD3)
04068 FoxO signaling pathway
102971888 (SMAD3)
09140 Cellular Processes
09141 Transport and catabolism
04144 Endocytosis
102971888 (SMAD3)
09143 Cell growth and death
04110 Cell cycle
102971888 (SMAD3)
04218 Cellular senescence
102971888 (SMAD3)
09144 Cellular community - eukaryotes
04520 Adherens junction
102971888 (SMAD3)
04550 Signaling pathways regulating pluripotency of stem cells
102971888 (SMAD3)
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
102971888 (SMAD3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102971888 (SMAD3)
09162 Cancer: specific types
05210 Colorectal cancer
102971888 (SMAD3)
05212 Pancreatic cancer
102971888 (SMAD3)
05225 Hepatocellular carcinoma
102971888 (SMAD3)
05226 Gastric cancer
102971888 (SMAD3)
05220 Chronic myeloid leukemia
102971888 (SMAD3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
102971888 (SMAD3)
05161 Hepatitis B
102971888 (SMAD3)
09163 Immune disease
05321 Inflammatory bowel disease
102971888 (SMAD3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
102971888 (SMAD3)
09167 Endocrine and metabolic disease
04933 AGE-RAGE signaling pathway in diabetic complications
102971888 (SMAD3)
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Ortholog
Paralog
GFIT
Motif
Pfam:
MH2
MH1
IRF-3
Motif
Other DBs
NCBI-GeneID:
102971888
NCBI-ProteinID:
XP_007084596
UniProt:
A0A8C9JVG8
LinkDB
All DBs
Position
Un
AA seq
320 aa
AA seq
DB search
MELCEFAFNMKKDEVCVNPYHYQRVETPVLPPVLVPRHTEIPAEFPPLDDYSHSIPENTN
FPAGIEPQSNIPETPPPGYLSEDGETSDHQMNHSMDAGSPNLSPNPMSPAHNNLDLQPVT
YCEPAFWCSISYYELNQRVGETFHASQPSMTVDGFTDPSNSERFCLGLLSNVNRNAAVEL
TRRHIGRGVRLYYIGGEVFAECLSDSAIFVQSPNCNQRYGWHPATVCKIPPGCNLKIFNN
QEFAALLAQSVNQGFEAVYQLTRMCTIRMSFVKGWGAEYRRQTVTSTPCWIELHLNGPLQ
WLDKVLTQMGSPSIRCSSVS
NT seq
963 nt
NT seq
+upstream
nt +downstream
nt
atggagctatgcgagttcgccttcaacatgaagaaggacgaggtctgcgtgaatccctac
cactatcagagggtagagaccccagttctacctcctgtgctggtgccacgccacacagag
atcccggccgagttccccccgctggacgactacagccattccatccccgagaacactaac
ttccccgcgggcatcgagccccagagcaatattccagaaaccccaccccctggctacctg
agtgaagatggagagaccagtgaccaccagatgaaccacagcatggatgcaggttctcca
aacctatccccgaatccgatgtccccagcacacaacaatttggacctgcagcctgtcacc
tactgcgagccagccttctggtgctccatttcctactacgagctgaaccagcgcgtcggg
gagaccttccacgcctcccagccctccatgaccgtggacggcttcaccgacccctccaac
tcggagcgcttctgcctggggctgctctccaatgtcaacaggaacgcggctgtggagctc
acacggaggcatatcgggcgaggcgtgcggctttactacatcggaggggaggtcttcgcc
gagtgcctcagtgacagcgccatttttgtccagtctcccaactgtaaccagcgctacggc
tggcacccagccaccgtctgcaagatcccgccaggatgcaacctgaagatcttcaacaac
caggagtttgccgccctcctggctcagtctgtcaaccagggcttcgaggcggtctaccag
ctgacccggatgtgcaccatccgcatgagcttcgtcaaaggctggggagcagagtacagg
agacagacagtgaccagcaccccctgctggattgagctgcacctgaatgggccgttgcag
tggcttgacaaggtcctcacccagatgggctccccaagcatccgctgttccagtgtgtct
tag
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integrated database retrieval system