Pan paniscus (bonobo): 100993322
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Entry
100993322 CDS
T02283
Symbol
SMAD3
Name
(RefSeq) mothers against decapentaplegic homolog 3 isoform X1
KO
K23605
mothers against decapentaplegic homolog 3
Organism
pps
Pan paniscus (bonobo)
Pathway
pps04068
FoxO signaling pathway
pps04110
Cell cycle
pps04144
Endocytosis
pps04218
Cellular senescence
pps04310
Wnt signaling pathway
pps04350
TGF-beta signaling pathway
pps04371
Apelin signaling pathway
pps04390
Hippo signaling pathway
pps04520
Adherens junction
pps04550
Signaling pathways regulating pluripotency of stem cells
pps04659
Th17 cell differentiation
pps04933
AGE-RAGE signaling pathway in diabetic complications
pps05161
Hepatitis B
pps05166
Human T-cell leukemia virus 1 infection
pps05200
Pathways in cancer
pps05210
Colorectal cancer
pps05212
Pancreatic cancer
pps05220
Chronic myeloid leukemia
pps05225
Hepatocellular carcinoma
pps05226
Gastric cancer
pps05321
Inflammatory bowel disease
pps05415
Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:
pps00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100993322 (SMAD3)
04350 TGF-beta signaling pathway
100993322 (SMAD3)
04390 Hippo signaling pathway
100993322 (SMAD3)
04371 Apelin signaling pathway
100993322 (SMAD3)
04068 FoxO signaling pathway
100993322 (SMAD3)
09140 Cellular Processes
09141 Transport and catabolism
04144 Endocytosis
100993322 (SMAD3)
09143 Cell growth and death
04110 Cell cycle
100993322 (SMAD3)
04218 Cellular senescence
100993322 (SMAD3)
09144 Cellular community - eukaryotes
04520 Adherens junction
100993322 (SMAD3)
04550 Signaling pathways regulating pluripotency of stem cells
100993322 (SMAD3)
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
100993322 (SMAD3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100993322 (SMAD3)
09162 Cancer: specific types
05210 Colorectal cancer
100993322 (SMAD3)
05212 Pancreatic cancer
100993322 (SMAD3)
05225 Hepatocellular carcinoma
100993322 (SMAD3)
05226 Gastric cancer
100993322 (SMAD3)
05220 Chronic myeloid leukemia
100993322 (SMAD3)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
100993322 (SMAD3)
05161 Hepatitis B
100993322 (SMAD3)
09163 Immune disease
05321 Inflammatory bowel disease
100993322 (SMAD3)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
100993322 (SMAD3)
09167 Endocrine and metabolic disease
04933 AGE-RAGE signaling pathway in diabetic complications
100993322 (SMAD3)
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Ortholog
Paralog
GFIT
Motif
Pfam:
MH2
MH1
IRF-3
Motif
Other DBs
NCBI-GeneID:
100993322
NCBI-ProteinID:
XP_003828052
Ensembl:
ENSPPAG00000033769
UniProt:
A0A2R9AV36
LinkDB
All DBs
Position
16:56319096..56448455
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
atgtcgtccatcctgcctttcactcccccgatcgtgaagcgcctgctgggctggaagaag
ggcgagcagaacgggcaggaggagaaatggtgcgagaaggcggtcaagagcctggtcaag
aaactcaaaaagacggggcagctggacgagctggagaaggccatcaccacgcagaacgtc
aacaccaagtgcatcaccatccccaggtccctggatggccggttgcaggtgtcccatcgg
aaggggctccctcatgtcatctactgccgcctgtggcgatggccagacctgcacagccac
cacgagctgcgggccatggagctgtgtgagttcgccttcaatatgaagaaggacgaggtc
tgcgtgaatccctaccactaccagagagtagagacaccagttctacctcctgtgttggtg
ccacgccacacagagatcccggccgagttccccccactggacgactacagccattccatc
cccgaaaacactaacttccccgcaggcatcgagccccagagcaatattccagagacccca
ccccctggctacctgagtgaagatggagaaaccagtgaccaccagatgaaccacagcatg
gacgcaggttctccaaacctatccccgaatccgatgtccccagcacataataacttggac
ctgcagccagttacctactgcgagccggccttctggtgctccatctcctactacgagctg
aaccagcgcgtcggggagacattccacgcctcgcagccatccatgactgtggatggcttc
accgacccctccaattcggagcgcttctgcctagggctgctctccaatgtcaacaggaat
gcagcagtggagctgacacggagacacatcggaagaggcgtgcggctctactacatcgga
ggggaggtcttcgcagagtgcctcagtgacagcgctatttttgtccagtctcccaactgt
aaccagcgctatggctggcacccggccaccgtctgcaagatcccaccaggatgcaacctg
aagatcttcaacaaccaggagttcgctgccctcctggcccagtccgtcaaccagggcttt
gaggctgtctaccagttgacccgaatgtgcaccatccgcatgagcttcgtcaaaggctgg
ggagcggagtacaggagacagactgtgaccagtaccccctgctggatcgagctgcacctg
aatgggcctttgcagtggcttgacaaggtcctcacccagatgggctccccaagcatccgc
tgttccagtgtgtcttag
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