KEGG   Rhinopithecus roxellana (golden snub-nosed monkey): 104682399
Entry
104682399         CDS       T03989                                 
Symbol
WNT3
Name
(RefSeq) proto-oncogene Wnt-3
  KO
K00312  wingless-type MMTV integration site family, member 3
Organism
rro  Rhinopithecus roxellana (golden snub-nosed monkey)
Pathway
rro04150  mTOR signaling pathway
rro04310  Wnt signaling pathway
rro04390  Hippo signaling pathway
rro04550  Signaling pathways regulating pluripotency of stem cells
rro04916  Melanogenesis
rro04934  Cushing syndrome
rro05010  Alzheimer disease
rro05022  Pathways of neurodegeneration - multiple diseases
rro05165  Human papillomavirus infection
rro05200  Pathways in cancer
rro05205  Proteoglycans in cancer
rro05206  MicroRNAs in cancer
rro05217  Basal cell carcinoma
rro05224  Breast cancer
rro05225  Hepatocellular carcinoma
rro05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:rro00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    104682399 (WNT3)
   04390 Hippo signaling pathway
    104682399 (WNT3)
   04150 mTOR signaling pathway
    104682399 (WNT3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    104682399 (WNT3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    104682399 (WNT3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    104682399 (WNT3)
   05206 MicroRNAs in cancer
    104682399 (WNT3)
   05205 Proteoglycans in cancer
    104682399 (WNT3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    104682399 (WNT3)
   05226 Gastric cancer
    104682399 (WNT3)
   05217 Basal cell carcinoma
    104682399 (WNT3)
   05224 Breast cancer
    104682399 (WNT3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    104682399 (WNT3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    104682399 (WNT3)
   05022 Pathways of neurodegeneration - multiple diseases
    104682399 (WNT3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    104682399 (WNT3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:rro00536]
    104682399 (WNT3)
Glycosaminoglycan binding proteins [BR:rro00536]
 Heparan sulfate / Heparin
  Morphogens
   104682399 (WNT3)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 104682399
NCBI-ProteinID: XP_010387342
UniProt: A0A2K6QK28
LinkDB
Position
19:73895896..73950517
AA seq 355 aa
MEPHLLGLLLGLLLGGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR
NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS
AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP
DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS
ASEMVVEKHRESRGWVETLRAKYSLFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC
NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECIRIYDVHTCK
NT seq 1068 nt   +upstreamnt  +downstreamnt
atggagccccacctgctcgggctgctcctcggcctcctgctcggtggcaccagggtcctc
gctggctacccaatttggtggtccctggccctgggccagcagtacacatctctgggctca
cagcccctgctctgcggctccatcccaggcctggtccccaagcaactgcgcttctgccgc
aattacatcgagatcatgcccagcgtggccgagggcgtgaaactgggcatccaggagtgc
cagcaccagttccggggccgccgctggaactgcaccaccatagatgacagcctggccatc
tttgggcccgtcctcgacaaagccacccgcgagtcggccttcgtgcacgccatcgcctcg
gccggcgtggccttcgccgtcacccgctcctgcgccgagggcacctccaccatttgcggc
tgtgactcgcatcataaggggccgcctggcgaaggctggaagtggggcggctgcagcgaa
gacgctgacttcggggtgttagtgtccagagagttcgcggacgcgcgtgagaacaggccg
gacgcacgctcggccatgaacaagcacaacaacgaggcgggccgcacgactatcctggac
cacatgcacctcaaatgcaagtgtcacgggctgtcgggcagctgtgaggtgaagacctgc
tggtgggcgcagcctgacttccgtgccattggcgacttcctcaaggacaagtatgacagc
gcctcggagatggtagtagagaagcaccgtgagtcccgaggctgggtggagaccctccgg
gccaagtactcgctcttcaagccgcccaccgagagggacctggtctactacgagaactcc
cccaacttttgtgagcccaacccagagacaggttcttttggcacaagggaccggacttgc
aatgtcacctcccatggcattgatggctgcgatctgctctgctgtggccgtggccacaac
acgaggacggagaagcggaaggaaaaatgccactgcatcttccactggtgctgctacgtc
agctgccaggagtgtattcgcatctacgatgtgcacacctgcaagtag

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