KEGG   Capra hircus (goat): 102169703
Entry
102169703         CDS       T02910                                 
Symbol
WNT3
Name
(RefSeq) proto-oncogene Wnt-3
  KO
K00312  wingless-type MMTV integration site family, member 3
Organism
chx  Capra hircus (goat)
Pathway
chx04150  mTOR signaling pathway
chx04310  Wnt signaling pathway
chx04390  Hippo signaling pathway
chx04550  Signaling pathways regulating pluripotency of stem cells
chx04916  Melanogenesis
chx04934  Cushing syndrome
chx05010  Alzheimer disease
chx05022  Pathways of neurodegeneration - multiple diseases
chx05165  Human papillomavirus infection
chx05200  Pathways in cancer
chx05205  Proteoglycans in cancer
chx05206  MicroRNAs in cancer
chx05217  Basal cell carcinoma
chx05224  Breast cancer
chx05225  Hepatocellular carcinoma
chx05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:chx00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102169703 (WNT3)
   04390 Hippo signaling pathway
    102169703 (WNT3)
   04150 mTOR signaling pathway
    102169703 (WNT3)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102169703 (WNT3)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102169703 (WNT3)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102169703 (WNT3)
   05206 MicroRNAs in cancer
    102169703 (WNT3)
   05205 Proteoglycans in cancer
    102169703 (WNT3)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102169703 (WNT3)
   05226 Gastric cancer
    102169703 (WNT3)
   05217 Basal cell carcinoma
    102169703 (WNT3)
   05224 Breast cancer
    102169703 (WNT3)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102169703 (WNT3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102169703 (WNT3)
   05022 Pathways of neurodegeneration - multiple diseases
    102169703 (WNT3)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102169703 (WNT3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:chx00536]
    102169703 (WNT3)
Glycosaminoglycan binding proteins [BR:chx00536]
 Heparan sulfate / Heparin
  Morphogens
   102169703 (WNT3)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 102169703
NCBI-ProteinID: XP_017920764
LinkDB
Position
19:45013255..45067683
AA seq 355 aa
MEPHLLRLLLGLLLGGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR
NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS
AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP
DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS
ASEMVVEKHRESRGWVETLRAKYALFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC
NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECVRIYDVHTCK
NT seq 1068 nt   +upstreamnt  +downstreamnt
atggagccccacctgctccggctgctcctcggcctcctgctcggtggcaccagggtcctc
gccggctacccaatttggtggtccctggcactgggccagcagtacacatccctgggctca
cagcccctactctgcggctccatcccaggcctggtccccaagcagctgcgcttctgccgc
aattacatcgaaatcatgcccagcgtggcagagggcgtgaagctgggcatccaggagtgc
cagcaccagtttcggggccgccgctggaactgcaccaccatcgacgacagcctggccatc
ttcgggcccgtcctcgacaaagccacccgagaatcggccttcgtgcacgccattgcctca
gccggcgtggcctttgcagtcacgcgctcctgtgcggagggcacctccaccatctgtggc
tgcgactcacatcacaaggggccgcctggcgagggctggaaatggggcggctgcagcgag
gatgctgacttcggggtgcttgtgtcccgagagttcgcagatgcacgtgagaacaggcca
gacgcgcgctcagccatgaacaagcacaacaacgaggctggccgcacgaccatcctggac
cacatgcatctcaagtgcaagtgccatgggctgtcgggcagctgtgaggtcaagacctgc
tggtgggcccagcccgacttccgcgccatcggcgacttcctcaaggacaagtacgacagc
gcctcggagatggtggtggagaagcatcgggagtcccgcggctgggtggagaccctccgc
gccaagtacgcgctcttcaagccgcccaccgagagggacctggtctactacgagaactcg
cccaacttttgcgagcccaaccccgagacgggctccttcggtaccagggaccggacttgc
aatgtcacctcccacggcatcgacggctgcgacctgctctgctgcggccgcggccacaac
acgaggacggagaagcggaaggagaaatgtcactgcatcttccactggtgttgctatgtg
agctgccaggagtgtgtccgcatctatgacgtgcacacctgcaagtag

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