KEGG   Neogale vison (American mink): 122906111
Entry
122906111         CDS       T08764                                 
Symbol
WNT3
Name
(RefSeq) proto-oncogene Wnt-3
  KO
K00312  wingless-type MMTV integration site family, member 3
Organism
nvs  Neogale vison (American mink)
Pathway
nvs04150  mTOR signaling pathway
nvs04310  Wnt signaling pathway
nvs04390  Hippo signaling pathway
nvs04550  Signaling pathways regulating pluripotency of stem cells
nvs04916  Melanogenesis
nvs04934  Cushing syndrome
nvs05010  Alzheimer disease
nvs05022  Pathways of neurodegeneration - multiple diseases
nvs05165  Human papillomavirus infection
nvs05200  Pathways in cancer
nvs05205  Proteoglycans in cancer
nvs05206  MicroRNAs in cancer
nvs05217  Basal cell carcinoma
nvs05224  Breast cancer
nvs05225  Hepatocellular carcinoma
nvs05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    122906111 (WNT3)
   04390 Hippo signaling pathway
    122906111 (WNT3)
   04150 mTOR signaling pathway
    122906111 (WNT3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    122906111 (WNT3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    122906111 (WNT3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    122906111 (WNT3)
   05206 MicroRNAs in cancer
    122906111 (WNT3)
   05205 Proteoglycans in cancer
    122906111 (WNT3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    122906111 (WNT3)
   05226 Gastric cancer
    122906111 (WNT3)
   05217 Basal cell carcinoma
    122906111 (WNT3)
   05224 Breast cancer
    122906111 (WNT3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    122906111 (WNT3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122906111 (WNT3)
   05022 Pathways of neurodegeneration - multiple diseases
    122906111 (WNT3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    122906111 (WNT3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:nvs00536]
    122906111 (WNT3)
Glycosaminoglycan binding proteins [BR:nvs00536]
 Heparan sulfate / Heparin
  Morphogens
   122906111 (WNT3)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 122906111
NCBI-ProteinID: XP_044103650
LinkDB
Position
5:complement(17341149..17389021)
AA seq 355 aa
MEPHLLGLLLGLLLCGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR
NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS
AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP
DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS
ASEMVVEKHRESRGWVETLRAKYALFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC
NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECVRIYDVHTCK
NT seq 1068 nt   +upstreamnt  +downstreamnt
atggagccccacctgctcgggctgctcctcggcctcctgctctgtggcaccagggtcctc
gccggctacccaatttggtggtccctggccctgggccagcaatacacatccctgggctca
cagcccctgctctgcggctccatcccgggcctggtccccaagcagctgcgcttctgccgg
aattacatcgagatcatgcccagtgtggccgagggcgtgaaactgggcatccaggagtgc
cagcaccagttccggggccgccgctggaactgtaccaccatagacgacagcctggccatc
ttcgggcccgtcctggacaaagccacccgtgagtcggccttcgtgcacgccattgcctct
gccggtgtggccttcgccgtcacgcgctcctgtgctgagggcacctccaccatctgcggc
tgtgactcgcaccacaaagggccgcctggcgagggctggaagtggggcggctgcagcgag
gacgccgacttcggggtgctcgtgtcccgggagttcgcagacgcgcgggagaacaggcca
gacgcgcgctcggccatgaacaagcacaacaatgaggcgggccgcacgaccatcctggac
cacatgcacctcaagtgcaagtgccacgggctgtccggcagctgcgaggtcaagacctgc
tggtgggcccaacccgacttccgcgctatcggcgacttcctcaaggacaagtacgacagt
gcctcggagatggtggtggagaagcaccgtgaatcccgcggctgggtggagaccctccgt
gccaagtatgcgctgttcaagccgcccaccgagagggacctggtctactacgagaactcc
cccaacttctgcgagcccaaccccgagacgggctcctttggcaccagggaccggacttgc
aatgtcacctcccacggcatcgacggctgcgacctactgtgctgcggccgcggccacaac
acgaggacggagaagcggaaggagaaatgccactgcatcttccactggtgctgctacgtg
agctgccaggagtgcgtccgcatctacgatgtgcacacctgcaagtag

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