KEGG   Piliocolobus tephrosceles (Ugandan red Colobus): 111528374
Entry
111528374         CDS       T07491                                 
Symbol
WNT3
Name
(RefSeq) proto-oncogene Wnt-3
  KO
K00312  wingless-type MMTV integration site family, member 3
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
pteh05206  MicroRNAs 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
    111528374 (WNT3)
   04390 Hippo signaling pathway
    111528374 (WNT3)
   04150 mTOR signaling pathway
    111528374 (WNT3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    111528374 (WNT3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    111528374 (WNT3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    111528374 (WNT3)
   05206 MicroRNAs in cancer
    111528374 (WNT3)
   05205 Proteoglycans in cancer
    111528374 (WNT3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    111528374 (WNT3)
   05226 Gastric cancer
    111528374 (WNT3)
   05217 Basal cell carcinoma
    111528374 (WNT3)
   05224 Breast cancer
    111528374 (WNT3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    111528374 (WNT3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    111528374 (WNT3)
   05022 Pathways of neurodegeneration - multiple diseases
    111528374 (WNT3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    111528374 (WNT3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pteh00536]
    111528374 (WNT3)
Glycosaminoglycan binding proteins [BR:pteh00536]
 Heparan sulfate / Heparin
  Morphogens
   111528374 (WNT3)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 111528374
NCBI-ProteinID: XP_023050831
Ensembl: ENSPTEG00000022807
UniProt: A0A8C9HRA1
LinkDB
Position
16:complement(54182217..54237318)
AA seq 355 aa
MEPHLLGLLLGLLLGGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR
NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS
AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP
DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS
ASEMVVEKHRESRGWVETLRAKYSLFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC
NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECIRIYDVHTCK
NT seq 1068 nt   +upstreamnt  +downstreamnt
atggagccccacctgctcgggctgctcctcggcctcctgctcggtggcaccagggtcctc
gctggctacccaatttggtggtccctggccctgggccagcagtacacatctctgggctca
cagcccctgctctgcggctccatcccaggcctggtccccaagcaactgcgcttctgccgc
aattacatcgagatcatgcccagcgtggccgagggcgtgaaattgggcatccaggagtgc
cagcaccagttccggggccgccgctggaactgcaccaccatagatgacagcctggccatc
ttcgggcccgtcctcgacaaagccacccgcgagtcggccttcgtgcacgccatcgcctcg
gccggcgtggccttcgccgtcacccgctcctgcgccgagggcacctccaccatttgcggc
tgcgactcgcatcataaggggccgcctggcgaaggctggaagtggggcggctgcagcgaa
gacgctgacttcggggtgttagtgtccagagagttcgcggacgcgcgtgagaacaggccg
gacgcacgctcggccatgaacaagcacaacaacgaggcgggccgcacgactatcctggac
cacatgcacctcaaatgcaagtgtcacgggctgtcgggcagctgtgaggtgaagacctgc
tggtgggcgcagcctgacttccgtgccattggcgacttcctcaaggacaagtatgacagc
gcctcagagatggtagtagagaagcaccgtgagtcccgaggctgggtggagaccctccgg
gccaagtactcgctcttcaagccgcccaccgagagggacctggtctactacgagaactcc
cccaacttttgtgagcccaacccagagacaggttcttttggcacaagggaccggacttgc
aatgtcacctcccatggcattgatggctgtgatctgctctgctgtggccgtggccacaac
acgaggacggagaagcggaaggaaaaatgccactgcatcttccactggtgctgctatgtc
agctgccaggagtgtattcgcatctacgatgtgcacacctgcaagtag

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