KEGG   Camelus ferus (Wild Bactrian camel): 102513805
Entry
102513805         CDS       T02979                                 
Symbol
WNT3
Name
(RefSeq) proto-oncogene Wnt-3 isoform X2
  KO
K00312  wingless-type MMTV integration site family, member 3
Organism
cfr  Camelus ferus (Wild Bactrian camel)
Pathway
cfr04150  mTOR signaling pathway
cfr04310  Wnt signaling pathway
cfr04390  Hippo signaling pathway
cfr04550  Signaling pathways regulating pluripotency of stem cells
cfr04916  Melanogenesis
cfr04934  Cushing syndrome
cfr05010  Alzheimer disease
cfr05022  Pathways of neurodegeneration - multiple diseases
cfr05165  Human papillomavirus infection
cfr05200  Pathways in cancer
cfr05205  Proteoglycans in cancer
cfr05206  MicroRNAs in cancer
cfr05217  Basal cell carcinoma
cfr05224  Breast cancer
cfr05225  Hepatocellular carcinoma
cfr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:cfr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102513805 (WNT3)
   04390 Hippo signaling pathway
    102513805 (WNT3)
   04150 mTOR signaling pathway
    102513805 (WNT3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102513805 (WNT3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102513805 (WNT3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102513805 (WNT3)
   05206 MicroRNAs in cancer
    102513805 (WNT3)
   05205 Proteoglycans in cancer
    102513805 (WNT3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102513805 (WNT3)
   05226 Gastric cancer
    102513805 (WNT3)
   05217 Basal cell carcinoma
    102513805 (WNT3)
   05224 Breast cancer
    102513805 (WNT3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102513805 (WNT3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102513805 (WNT3)
   05022 Pathways of neurodegeneration - multiple diseases
    102513805 (WNT3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102513805 (WNT3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:cfr00536]
    102513805 (WNT3)
Glycosaminoglycan binding proteins [BR:cfr00536]
 Heparan sulfate / Heparin
  Morphogens
   102513805 (WNT3)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 102513805
NCBI-ProteinID: XP_006194480
UniProt: A0A8B6YP11
LinkDB
Position
16:complement(34845694..34892463)
AA seq 355 aa
MEPHLLGLLLGLLLCGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR
NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS
AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP
DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS
ASEMVVEKHRESRGWVETLRAKYALFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC
NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECIRIYDVHTCK
NT seq 1068 nt   +upstreamnt  +downstreamnt
atggagccccacctgctcgggctgctcctcggcctcctgctctgtggcaccagggtcctc
gccggctacccaatttggtggtccctggccctgggccagcagtacacgtccctgggctca
cagcccctgctctgtggctccatcccaggcctggtccccaagcaactgcgcttctgccgc
aattacatcgaaatcatgcccagtgtggctgagggtgtgaagctgggcatccaggagtgc
cagcaccagttccgaggccgccgctggaactgcaccaccattgacgacagcctggccatc
ttcgggcccgtcctcgacaaagccacccgcgaatcagcctttgtgcatgccatcgcctca
gccggggtggcctttgctgtcacacgctcctgtgccgagggcacctccaccatctgtggc
tgtgattcgcatcataaggggccgcctggagagggctggaagtggggcggctgcagtgag
gacgccgacttcggggtgctcgtgtctcgggagtttgccgacgcacgcgagaacaggccg
gatgcccgctcggctatgaacaagcacaacaacgaggctggccgcacgaccatcctggac
cacatgcacctcaagtgcaagtgccatggactgtcaggcagctgcgaggtcaagacctgc
tggtgggcccagcccgacttccgcgccatcggtgacttcctcaaggacaagtacgacagc
gcctcagagatggtggtggagaagcaccgggagtcccgcggctgggtggagaccctccgt
gccaagtacgcgctcttcaagccacccacggagcgggacctggtctactacgagaactcc
cccaacttttgcgagcccaaccccgagacgggctcctttggcaccagggaccggacttgc
aatgtcacctcccacggcatcgatggctgtgacctgctctgctgcggccgcggccacaac
acaaggacggagaagcgcaaggagaaatgccactgcatcttccactggtgctgctatgtg
agctgccaggagtgcatccgcatctacgacgtgcacacctgcaagtag

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