KEGG   Mustela nigripes (black-footed ferret): 132003761
Entry
132003761         CDS       T09425                                 
Symbol
WNT3
Name
(RefSeq) proto-oncogene Wnt-3
  KO
K00312  wingless-type MMTV integration site family, member 3
Organism
mnp  Mustela nigripes (black-footed ferret)
Pathway
mnp04150  mTOR signaling pathway
mnp04310  Wnt signaling pathway
mnp04390  Hippo signaling pathway
mnp04550  Signaling pathways regulating pluripotency of stem cells
mnp04916  Melanogenesis
mnp04934  Cushing syndrome
mnp05010  Alzheimer disease
mnp05022  Pathways of neurodegeneration - multiple diseases
mnp05165  Human papillomavirus infection
mnp05200  Pathways in cancer
mnp05205  Proteoglycans in cancer
mnp05206  MicroRNAs in cancer
mnp05217  Basal cell carcinoma
mnp05224  Breast cancer
mnp05225  Hepatocellular carcinoma
mnp05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mnp00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    132003761 (WNT3)
   04390 Hippo signaling pathway
    132003761 (WNT3)
   04150 mTOR signaling pathway
    132003761 (WNT3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    132003761 (WNT3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    132003761 (WNT3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    132003761 (WNT3)
   05206 MicroRNAs in cancer
    132003761 (WNT3)
   05205 Proteoglycans in cancer
    132003761 (WNT3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    132003761 (WNT3)
   05226 Gastric cancer
    132003761 (WNT3)
   05217 Basal cell carcinoma
    132003761 (WNT3)
   05224 Breast cancer
    132003761 (WNT3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    132003761 (WNT3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    132003761 (WNT3)
   05022 Pathways of neurodegeneration - multiple diseases
    132003761 (WNT3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    132003761 (WNT3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mnp00536]
    132003761 (WNT3)
Glycosaminoglycan binding proteins [BR:mnp00536]
 Heparan sulfate / Heparin
  Morphogens
   132003761 (WNT3)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 132003761
NCBI-ProteinID: XP_059235479
LinkDB
Position
16:complement(17025193..17072436)
AA seq 355 aa
MEPHLLGLLLGLLLCGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR
NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS
AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP
DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS
ASEMVVEKHRESRGWVETLRAKYALFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC
NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECVRIYDVHTCK
NT seq 1068 nt   +upstreamnt  +downstreamnt
atggagccccacctgctcgggctgctcctcggcctcctgctctgtggcaccagggtcctc
gccggctacccaatttggtggtccctggccctgggccagcaatacacatccctgggttcg
cagcccctgctctgcggctccatcccgggcctggtccccaagcagctgcgcttctgccgg
aattacatcgagatcatgcccagtgtggccgagggcgtgaaactgggcatccaggagtgc
cagcaccagttccggggccgccgctggaactgcaccaccatagacgacagcctggccatc
tttgggcccgtcctggacaaagccacccgcgagtcggccttcgtgcacgccatcgcctct
gccggtgtggccttcgccgtcacgcgctcctgtgctgagggcacctccaccatctgcggc
tgcgactcgcaccacaaagggccgcctggcgagggctggaagtggggcggctgcagcgag
gacgccgacttcggggtgctcgtgtcccgggagttcgcagacgcgcgcgagaacaggcca
gacgcgcgctcggccatgaacaagcacaacaacgaggcgggccgcacgaccatcctggac
cacatgcacctcaagtgcaagtgccacgggctgtccggcagctgcgaggtcaagacctgc
tggtgggcccaacccgacttccgcgcaatcggcgacttcctcaaggacaagtacgacagt
gcctcggagatggtggtggagaagcaccgtgaatcccgcggctgggtggagaccctccgt
gccaagtatgcgctgttcaagccgcccaccgagagggacctggtctactacgagaactcc
cccaacttctgcgagcccaaccctgagacgggctcctttggcaccagggaccggacttgc
aatgtcacctcccacggcatcgatggctgcgacctgctgtgctgtggccgcggccacaac
acgaggacggagaagcggaaggagaaatgccactgcatcttccactggtgctgctacgtg
agctgccaggagtgcgtccgcatctacgatgtgcacacctgcaagtag

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