KEGG   Mustela putorius furo (domestic ferret): 101692089
Entry
101692089         CDS       T07239                                 
Symbol
WNT6
Name
(RefSeq) protein Wnt-6
  KO
K00445  wingless-type MMTV integration site family, member 6
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
    101692089 (WNT6)
   04390 Hippo signaling pathway
    101692089 (WNT6)
   04150 mTOR signaling pathway
    101692089 (WNT6)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101692089 (WNT6)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    101692089 (WNT6)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101692089 (WNT6)
   05205 Proteoglycans in cancer
    101692089 (WNT6)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101692089 (WNT6)
   05226 Gastric cancer
    101692089 (WNT6)
   05217 Basal cell carcinoma
    101692089 (WNT6)
   05224 Breast cancer
    101692089 (WNT6)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101692089 (WNT6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101692089 (WNT6)
   05022 Pathways of neurodegeneration - multiple diseases
    101692089 (WNT6)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101692089 (WNT6)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mpuf00536]
    101692089 (WNT6)
Glycosaminoglycan binding proteins [BR:mpuf00536]
 Heparan sulfate / Heparin
  Morphogens
   101692089 (WNT6)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 101692089
NCBI-ProteinID: XP_004762845
Ensembl: ENSMPUG00000016550
UniProt: M3YYN7
LinkDB
Position
Unknown
AA seq 365 aa
MLPPAPSLLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPPGLPGTPGPPGPAGSPDGSAAWEWGGCGDDVDFGD
EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSTAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE
LSLCL
NT seq 1098 nt   +upstreamnt  +downstreamnt
atgctgccgcccgcgccctccctcctcgggctgctgctgctgctcctcctgtgtcccgcg
cacgtcggtggactgtggtgggcggtgggcagccccctggtcatggaccccaccagcatc
tgcaggaaagcacggcggctggcaggacggcaagccgagctgtgccaggccgagccagaa
gtggtggcggagctagcccggggcgcccggcttggggtgcgagagtgccagttccagttc
cgtttccgccgctggaactgctccagccacagcaaggcctttgggcgcatcctgcagcag
gacatccgggagaccgccttcgtgtttgcgattactgctgcgggcgccagccacgcggtt
acgcaggcctgctctatgggtgagctgctgcagtgcggctgccaggcaccccgcgggcgg
gccccgccccgccccccgggtctgccgggcacccccgggcccccgggccccgccggctcc
cccgatggcagcgccgcctgggagtggggaggctgcggcgacgacgtggacttcggggac
gagaagtcgaggctcttcatggatgcgcggcacaagcggggtcgcggagacatccgtgcc
ttagtgcaacttcacaacaatgaggcgggccggctggccgtgcggagccatacgcgcacc
gagtgcaagtgtcacgggctgtcgggctcgtgcgcgctgcggacctgctggcagaagctg
cccccgttccgcgaggtgggcgcgcggctgctcgagcgcttccacggcgcctcgcgtgtt
atgggaaccaacgacggcaaggctctgctgcccgcggtccgcactctcaagccgcctggc
cgcgccgacctcctctacgcagccgactcgcccgacttctgcgctcccaacaggcgcacc
ggctcgcccggcacgcgtggccgcgcctgcaacagcaccgctccggacctcagcggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcaactcgaggagaactgc
ctgtgccgcttccattggtgctgcgtcgttcagtgccatcgctgtcgcgtgcgcaaggag
ctcagcctctgcctctga

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