KEGG   Neogale vison (American mink): 122894006
Entry
122894006         CDS       T08764                                 
Symbol
SMAD3
Name
(RefSeq) mothers against decapentaplegic homolog 3 isoform X1
  KO
K23605  mothers against decapentaplegic homolog 3
Organism
nvs  Neogale vison (American mink)
Pathway
nvs04068  FoxO signaling pathway
nvs04110  Cell cycle
nvs04144  Endocytosis
nvs04218  Cellular senescence
nvs04310  Wnt signaling pathway
nvs04350  TGF-beta signaling pathway
nvs04371  Apelin signaling pathway
nvs04390  Hippo signaling pathway
nvs04520  Adherens junction
nvs04550  Signaling pathways regulating pluripotency of stem cells
nvs04659  Th17 cell differentiation
nvs04933  AGE-RAGE signaling pathway in diabetic complications
nvs05161  Hepatitis B
nvs05166  Human T-cell leukemia virus 1 infection
nvs05200  Pathways in cancer
nvs05210  Colorectal cancer
nvs05212  Pancreatic cancer
nvs05220  Chronic myeloid leukemia
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
   04310 Wnt signaling pathway
    122894006 (SMAD3)
   04350 TGF-beta signaling pathway
    122894006 (SMAD3)
   04390 Hippo signaling pathway
    122894006 (SMAD3)
   04371 Apelin signaling pathway
    122894006 (SMAD3)
   04068 FoxO signaling pathway
    122894006 (SMAD3)
 09140 Cellular Processes
  09141 Transport and catabolism
   04144 Endocytosis
    122894006 (SMAD3)
  09143 Cell growth and death
   04110 Cell cycle
    122894006 (SMAD3)
   04218 Cellular senescence
    122894006 (SMAD3)
  09144 Cellular community - eukaryotes
   04520 Adherens junction
    122894006 (SMAD3)
   04550 Signaling pathways regulating pluripotency of stem cells
    122894006 (SMAD3)
 09150 Organismal Systems
  09151 Immune system
   04659 Th17 cell differentiation
    122894006 (SMAD3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    122894006 (SMAD3)
  09162 Cancer: specific types
   05210 Colorectal cancer
    122894006 (SMAD3)
   05212 Pancreatic cancer
    122894006 (SMAD3)
   05225 Hepatocellular carcinoma
    122894006 (SMAD3)
   05226 Gastric cancer
    122894006 (SMAD3)
   05220 Chronic myeloid leukemia
    122894006 (SMAD3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    122894006 (SMAD3)
   05161 Hepatitis B
    122894006 (SMAD3)
  09163 Immune disease
   05321 Inflammatory bowel disease
    122894006 (SMAD3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    122894006 (SMAD3)
  09167 Endocrine and metabolic disease
   04933 AGE-RAGE signaling pathway in diabetic complications
    122894006 (SMAD3)
SSDB
Motif
Pfam: MH2 MH1 IRF-3
Other DBs
NCBI-GeneID: 122894006
NCBI-ProteinID: XP_044087303
UniProt: A0A8C7B9N7
LinkDB
Position
13:complement(99716895..99833260)
AA seq 425 aa
MSSILPFTPPIVKRLLGWKKGEQNGQEEKWCEKAVKSLVKKLKKTGQLDELEKAITTQNV
NTKCITIPRSLDGRLQVSHRKGLPHVIYCRLWRWPDLHSHHELRAMELCEFAFNMKKDEV
CVNPYHYQRVETPVLPPVLVPRHTEIPAEFPPLDDYSHSIPENTNFPAGIEPQSNIPETP
PPGYLSEDGETSDHQMNHSMDAGSPNLSPNPMSPAHNNLDLQPVTYCEPAFWCSISYYEL
NQRVGETFHASQPSMTVDGFTDPSNSERFCLGLLSNVNRNAAVELTRRHIGRGVRLYYIG
GEVFAECLSDSAIFVQSPNCNQRYGWHPATVCKIPPGCNLKIFNNQEFAALLAQSVNQGF
EAVYQLTRMCTIRMSFVKGWGAEYRRQTVTSTPCWIELHLNGPLQWLDKVLTQMGSPSIR
CSSVS
NT seq 1278 nt   +upstreamnt  +downstreamnt
atgtcgtccatcctgcccttcacccccccgatcgtgaagcgcctgctgggctggaagaag
ggcgagcagaacgggcaggaggagaagtggtgcgagaaggcggtcaagagtttggtcaag
aagctcaagaagacggggcagctggacgaactggagaaggccatcaccacgcagaacgtc
aacaccaagtgcatcaccatccccaggtccctggatggccgcctgcaggtgtcccatcgg
aaggggctcccccatgtcatctactgccgcctgtggcgatggcccgacctgcacagccac
cacgagctgcgggccatggagctgtgtgagttcgccttcaacatgaagaaggacgaggtc
tgcgtgaatccctaccactatcagagggtagagaccccagttctacctcctgtgctggtc
ccacgccacacagagatcccggccgagttccccccgctggacgactacagccattccatc
cccgagaacacgaacttccccgcgggcatcgagccccagagcaatattccagaaacccca
ccccctggctacctgagtgaagatggagagaccagtgaccaccagatgaaccacagcatg
gatgcaggttctccaaacctatccccgaatccgatgtccccagcgcacaataatttggac
ctgcagcctgtcacctactgcgagccagccttctggtgctccatctcctactatgaactg
aaccagcgcgttggggaaacattccacgcctcgcagccttccatgaccgtggacggcttc
accgacccctccaattcggagcgcttctgcctggggctgctctccaacgtcaacaggaac
gcggctgtggagctcacgcggaggcacatcgggcgaggcgtgcggctgtactacattgga
ggggaggtcttcgcagagtgcctcagcgacagcgccatcttcgtccagtcgcccaactgt
aaccagcgctatggctggcacccggccaccgtctgtaagatcccgccagggtgcaacctg
aagatcttcaacaaccaggagtttgccgccctcctggctcagtccgtcaaccagggcttc
gaggcggtctaccagttgacccggatgtgcaccatccgcatgagcttcgtcaaaggctgg
ggagcggaatacaggagacaaacggtgaccagcaccccctgctggattgagctgcacctg
aatgggcctttgcagtggcttgacaaggtcctcactcagatgggctccccaagcatccgc
tgttccagtgtgtcttag

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