KEGG   Piliocolobus tephrosceles (Ugandan red Colobus): 111546073
Entry
111546073         CDS       T07491                                 
Symbol
WNT6
Name
(RefSeq) protein Wnt-6
  KO
K00445  wingless-type MMTV integration site family, member 6
Organism
pteh  Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh04150  mTOR signaling pathway
pteh04310  Wnt signaling pathway
pteh04390  Hippo signaling pathway
pteh04550  Signaling pathways regulating pluripotency of stem cells
pteh04916  Melanogenesis
pteh04934  Cushing syndrome
pteh05010  Alzheimer disease
pteh05022  Pathways of neurodegeneration - multiple diseases
pteh05165  Human papillomavirus infection
pteh05200  Pathways in cancer
pteh05205  Proteoglycans in cancer
pteh05217  Basal cell carcinoma
pteh05224  Breast cancer
pteh05225  Hepatocellular carcinoma
pteh05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pteh00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    111546073 (WNT6)
   04390 Hippo signaling pathway
    111546073 (WNT6)
   04150 mTOR signaling pathway
    111546073 (WNT6)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    111546073 (WNT6)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    111546073 (WNT6)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    111546073 (WNT6)
   05205 Proteoglycans in cancer
    111546073 (WNT6)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    111546073 (WNT6)
   05226 Gastric cancer
    111546073 (WNT6)
   05217 Basal cell carcinoma
    111546073 (WNT6)
   05224 Breast cancer
    111546073 (WNT6)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    111546073 (WNT6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    111546073 (WNT6)
   05022 Pathways of neurodegeneration - multiple diseases
    111546073 (WNT6)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    111546073 (WNT6)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pteh00536]
    111546073 (WNT6)
Glycosaminoglycan binding proteins [BR:pteh00536]
 Heparan sulfate / Heparin
  Morphogens
   111546073 (WNT6)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 111546073
NCBI-ProteinID: XP_023073127
Ensembl: ENSPTEG00000039168
UniProt: A0A8C9M0D4
LinkDB
Position
11:105332130..105346632
AA seq 365 aa
MLPPAPSRLGLLLLLLLCPAHVGGLWWAVGSPLVMDPISICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPSGLPGTPGPPGPVGSPEGSSAWEWGGCGDDVDFGD
EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE
LNLCL
NT seq 1098 nt   +upstreamnt  +downstreamnt
atgctgccgcccgcgccctcccgcctcgggctgctgctgctgctgctcctgtgcccagcg
cacgtcggcggactgtggtgggctgtgggcagtcccttggttatggaccctatcagcatc
tgcaggaaggcacggcggctggccgggaggcaggccgagttgtgccaggctgagccagaa
gtagtggcagagctagcccggggcgcccggctcggggtgcgagagtgccagttccagttc
cgcttccgccgctggaactgctccagccacagcaaggcctttggacgcatcctgcagcag
gacattcgagagacggccttcgtgttcgccatcactgcggcgggcgccagccacgccgtc
acgcaggcctgttccatgggcgaactgctgcagtgcggctgccaggcgccccgcgggcgg
gcccctccccggccctctggcctgcccggcacccccggaccccctggccccgtgggctcc
ccggaaggcagctctgcctgggagtggggaggctgcggcgacgacgtggacttcggggac
gagaagtcgaggctctttatggacgcgcggcacaagcggggacgcggagacatccgcgcg
ttggtgcaactgcacaacaacgaggcgggccggctggccgtgcggagccacacgcgcacc
gagtgcaaatgccacgggctgtcgggctcgtgcgcgctgcgaacctgctggcagaagctg
cctccgtttcgcgaggtgggcgcgcggctgctggagcgcttccacggcgcctcacgcgtc
atgggcactaacgacggcaaggccctactgcccgccgtgcgcacgctcaagccgccgggc
cgagcggacctgctctacgccgctgattcgcccgacttctgcgcccccaaccgacgcacc
ggctcccccggcacgcgcggccgcgcctgcaatagcagcgccccggacctcagtggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcagctcgaagagaactgc
ctgtgccgtttccactggtgctgcgtagtgcagtgccaccgctgccgtgtgcgcaaggag
ctcaacctctgcctctga

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