Rousettus aegyptiacus (Egyptian rousette): 107512852
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Entry
107512852 CDS
T06036
Gene name
SMAD4
Definition
(RefSeq) mothers against decapentaplegic homolog 4 isoform X1
KO
K04501
mothers against decapentaplegic homolog 4
Organism
ray
Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04068
FoxO signaling pathway
ray04110
Cell cycle
ray04310
Wnt signaling pathway
ray04350
TGF-beta signaling pathway
ray04371
Apelin signaling pathway
ray04390
Hippo signaling pathway
ray04520
Adherens junction
ray04550
Signaling pathways regulating pluripotency of stem cells
ray04659
Th17 cell differentiation
ray04933
AGE-RAGE signaling pathway in diabetic complications
ray05161
Hepatitis B
ray05166
Human T-cell leukemia virus 1 infection
ray05200
Pathways in cancer
ray05210
Colorectal cancer
ray05212
Pancreatic cancer
ray05220
Chronic myeloid leukemia
ray05225
Hepatocellular carcinoma
ray05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ray00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
107512852 (SMAD4)
04350 TGF-beta signaling pathway
107512852 (SMAD4)
04390 Hippo signaling pathway
107512852 (SMAD4)
04371 Apelin signaling pathway
107512852 (SMAD4)
04068 FoxO signaling pathway
107512852 (SMAD4)
09140 Cellular Processes
09143 Cell growth and death
04110 Cell cycle
107512852 (SMAD4)
09144 Cellular community - eukaryotes
04520 Adherens junction
107512852 (SMAD4)
04550 Signaling pathways regulating pluripotency of stem cells
107512852 (SMAD4)
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
107512852 (SMAD4)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
107512852 (SMAD4)
09162 Cancer: specific types
05210 Colorectal cancer
107512852 (SMAD4)
05212 Pancreatic cancer
107512852 (SMAD4)
05225 Hepatocellular carcinoma
107512852 (SMAD4)
05226 Gastric cancer
107512852 (SMAD4)
05220 Chronic myeloid leukemia
107512852 (SMAD4)
09167 Endocrine and metabolic disease
04933 AGE-RAGE signaling pathway in diabetic complications
107512852 (SMAD4)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
107512852 (SMAD4)
05161 Hepatitis B
107512852 (SMAD4)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
MH2
MH1
IRF-3
Motif
Other DBs
NCBI-GeneID:
107512852
NCBI-ProteinID:
XP_016004265
LinkDB
All DBs
Position
Unknown
AA seq
552 aa
AA seq
DB search
MDNMSITNTPTSNDACLSIVHSLMCHRQGGESETFAKRAIESLVKKLKEKKDELDSLITA
ITTNGAHPSKCVTIQRTLDGRLQVAGRKGFPHVIYARLWRWPDLHKNELKHVKYCQYAFD
LKCDSVCVNPYHYERVVSPGIDLSGLTLQSNAPPSMLVKDEYVHDFEGQPSLSTEGHSIQ
TIQHPPSNRASTESYSTPALLASSESNATSTTNFPNIPVASTSQPASILAGSHSEGLLQI
ASGPQPGQQQNGFTGQPATYHHNSTTTWTGSRTAPYTPNLPHHQNGHLQHHPPMPPHPGH
YWPVHNELAFQPPISNHPAPEYWCSIAYFEMDVQVGETFKVPSSCPIVTVDGYVDPSGGD
RFCLGQLSNVHRTEAIERARLHIGKGVQLECKGEGDVWVRCLSDHAVFVQSYYLDREAGR
APGDAVHKIYPSAYIKVFDLRQCHRQMQQQAATAQAAAAAQAAAVAGNIPGPGSVGGIAP
AISLSAAAGIGVDDLRRLCILRMSFVKGWGPDYPRQSIKETPCWIEIHLHRALQLLDEVL
HTMPIADPQPLD
NT seq
1659 nt
NT seq
+upstream
nt +downstream
nt
atggacaatatgtctattacaaatacaccaacaagtaatgatgcctgtctgagcattgta
catagtttgatgtgccatagacaaggtggagagagtgaaacatttgcaaaaagagcaatt
gaaagtttggtaaagaaactgaaggagaaaaaggatgaattggattctttaataacagct
ataactacaaatggagctcatcctagcaaatgtgttaccatacagagaacattggatgga
aggcttcaggttgccggtcggaaaggatttcctcatgtgatctatgcccgtctctggagg
tggcctgatcttcacaaaaatgaactaaaacatgttaaatattgtcagtatgcatttgac
ttaaaatgtgacagtgtctgtgtgaatccatatcactatgaacgagttgtatcaccggga
attgatctctcaggattaacactgcagagtaatgctccaccaagtatgttggtgaaggat
gaatatgttcatgacttcgagggacagccatcgttatccacggaagggcattcaattcaa
accatccaacatccaccaagtaatcgtgcttcaacagagtcatacagcaccccagctctg
ttagcttcatctgagtctaatgctaccagcaccaccaactttcccaacattcctgtggct
tccacaagtcagcctgccagtatactggcaggcagccatagtgaaggattgttgcagata
gcttcagggcctcagccaggacagcagcagaatggatttactggtcagccagctacttac
catcataacagcactaccacctggactggaagtaggactgcaccatacacacctaatttg
cctcaccaccaaaacggccatcttcagcaccacccgcctatgccgccccatcccggacat
tactggccagttcacaatgagcttgcattccagcctcccatttctaatcatcctgctcct
gagtattggtgttccatcgcttactttgaaatggatgttcaagtaggagagacatttaag
gttccttcaagctgccctattgttactgttgatggatatgtggacccttctggtggagat
cgcttttgcttgggtcaactttccaacgtccacaggacagaagccattgagagagcaagg
ttgcacataggcaaaggtgtgcagttggaatgtaaaggggaaggtgatgtttgggtcagg
tgccttagcgaccatgcagtctttgtacagagttactacttagacagagaagctgggcgt
gcacctggagatgctgttcataagatctacccaagtgcatatataaaggtctttgatttg
cggcagtgtcatcggcagatgcagcagcaggcggccaccgcacaagctgcagcagctgcc
caggcagcagccgtggccggaaacatccctggcccaggatcagtaggtggaatagctcca
gctatcagtttgtccgctgctgctggaatcggtgttgatgaccttcgccgcttatgcata
ctcaggatgagtttcgtgaagggctggggaccggattacccaagacagagcatcaaagaa
acgccttgctggatcgagattcacttacaccgggctctccagctcctagatgaagttctt
cacaccatgcctattgccgacccacaacctttagactga
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