KEGG   Mustela putorius furo (domestic ferret): 101680529
Entry
101680529         CDS       T07239                                 
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
mpuf  Mustela putorius furo (domestic ferret)
Pathway
mpuf04150  mTOR signaling pathway
mpuf04310  Wnt signaling pathway
mpuf04390  Hippo signaling pathway
mpuf04550  Signaling pathways regulating pluripotency of stem cells
mpuf04916  Melanogenesis
mpuf04934  Cushing syndrome
mpuf05010  Alzheimer disease
mpuf05022  Pathways of neurodegeneration - multiple diseases
mpuf05165  Human papillomavirus infection
mpuf05200  Pathways in cancer
mpuf05205  Proteoglycans in cancer
mpuf05217  Basal cell carcinoma
mpuf05224  Breast cancer
mpuf05225  Hepatocellular carcinoma
mpuf05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mpuf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101680529 (WNT11)
   04390 Hippo signaling pathway
    101680529 (WNT11)
   04150 mTOR signaling pathway
    101680529 (WNT11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101680529 (WNT11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    101680529 (WNT11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101680529 (WNT11)
   05205 Proteoglycans in cancer
    101680529 (WNT11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101680529 (WNT11)
   05226 Gastric cancer
    101680529 (WNT11)
   05217 Basal cell carcinoma
    101680529 (WNT11)
   05224 Breast cancer
    101680529 (WNT11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101680529 (WNT11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101680529 (WNT11)
   05022 Pathways of neurodegeneration - multiple diseases
    101680529 (WNT11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101680529 (WNT11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mpuf00536]
    101680529 (WNT11)
Glycosaminoglycan binding proteins [BR:mpuf00536]
 Heparan sulfate / Heparin
  Morphogens
   101680529 (WNT11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 101680529
NCBI-ProteinID: XP_004768063
Ensembl: ENSMPUG00000008789
UniProt: M3YBL2
LinkDB
Position
Unknown
AA seq 354 aa
MRARPRVCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTVVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSHGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq 1065 nt   +upstreamnt  +downstreamnt
atgagggcgcggccgcgggtctgcgaggcgctcctcttcgccctggcgctccagaccggc
gtatgctacggcatcaagtggctggcactgtccaagaccccggcggccctggcgttgaac
cagacgcagcactgcaagcagctggaggggctggtgtctgcacaggtgcagctctgccgc
agcaacctggagctcatgcacaccgtcgtgcacgccgcccgcgaggtcatgaaggcctgc
cgcagggcattcgccgacatgcgctggaactgctcctccatcgagcttgcccccaactac
ctgcttgacctggagagagggacgcgggagtcagccttcgtgtatgcgctgtcggcggcc
gccatcagccacgccatcgcccgggcctgcacctccggcgacctgcccggctgctcctgc
ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgcgcctctctggaaatgaagtgtaagtgccacggggtgtctggctcctgctctatc
cgcacctgctggaaggggctgcaggagctccgggatgtggccgctgacctcaagacccgc
tacctgtcggccaccaaggtcgtgcaccgacccatgggcacccgcaagcacctggtgccc
aaggacctggatatcaggcccgtgaaggactcggagcttgtctatctgcagagctcaccc
gacttctgcatgaagaacgagaaggtgggctcccatggaacgcaagacaggcagtgcaac
aagacatcccacggcagtgacagctgtgacctcatgtgctgcggccgcggctacaaccct
tacacggaccgcgtcgttgagcgctgccactgcaagtaccactggtgctgctacgtcacg
tgccgtcgctgtgagcgcacggtggagcgctatgtctgcaagtga

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