KEGG   Prionailurus viverrinus (fishing cat): 125160069
Entry
125160069         CDS       T09889                                 
Symbol
WNT3A
Name
(RefSeq) protein Wnt-3a
  KO
K00312  wingless-type MMTV integration site family, member 3
Organism
pviv  Prionailurus viverrinus (fishing cat)
Pathway
pviv04150  mTOR signaling pathway
pviv04310  Wnt signaling pathway
pviv04390  Hippo signaling pathway
pviv04550  Signaling pathways regulating pluripotency of stem cells
pviv04916  Melanogenesis
pviv04934  Cushing syndrome
pviv05010  Alzheimer disease
pviv05022  Pathways of neurodegeneration - multiple diseases
pviv05165  Human papillomavirus infection
pviv05200  Pathways in cancer
pviv05205  Proteoglycans in cancer
pviv05206  MicroRNAs in cancer
pviv05217  Basal cell carcinoma
pviv05224  Breast cancer
pviv05225  Hepatocellular carcinoma
pviv05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pviv00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    125160069 (WNT3A)
   04390 Hippo signaling pathway
    125160069 (WNT3A)
   04150 mTOR signaling pathway
    125160069 (WNT3A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    125160069 (WNT3A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    125160069 (WNT3A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    125160069 (WNT3A)
   05206 MicroRNAs in cancer
    125160069 (WNT3A)
   05205 Proteoglycans in cancer
    125160069 (WNT3A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    125160069 (WNT3A)
   05226 Gastric cancer
    125160069 (WNT3A)
   05217 Basal cell carcinoma
    125160069 (WNT3A)
   05224 Breast cancer
    125160069 (WNT3A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    125160069 (WNT3A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    125160069 (WNT3A)
   05022 Pathways of neurodegeneration - multiple diseases
    125160069 (WNT3A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    125160069 (WNT3A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pviv00536]
    125160069 (WNT3A)
Glycosaminoglycan binding proteins [BR:pviv00536]
 Heparan sulfate / Heparin
  Morphogens
   125160069 (WNT3A)
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 125160069
NCBI-ProteinID: XP_047704575
LinkDB
Position
Unknown
AA seq 352 aa
MALLVYFLFLYGLKQALGSYPIWWSLAIGPQYSSLGTQPILCASIPGLVPKQLRFCRNYV
EIMPSVAEGIKISIQECQHQFRGRRWNCTTVNNSLAIFGPVLDKATRESAFVHAIASAGV
AFAVTRSCAEGSATICGCSSRHQGSPGEGWKWGGCSEDIEFGGMVSREFADARENRPDAR
SAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRAIGDFLKDKYDSASE
MVVEKHRESRGWVETLRPRYTYFKVPTDRDLVYYEASPNFCEPNPETGSFGTRDRTCNVS
SHGIDGCDLLCCGRGHNARTERRREKCHCVFHWCCYVSCQECSRVYDVHTCK
NT seq 1059 nt   +upstreamnt  +downstreamnt
atggccctgctcgtatacttcttattcctctacggcctgaagcaggcgctgggcagttac
ccgatctggtggtccttggccattgggccccagtactcatccctgggcactcagcccatc
ctgtgtgccagcatcccgggcctggtgcccaagcagctgcggttctgccggaactacgtg
gagattatgcccagcgtggcggagggcatcaagataagcattcaggagtgccagcaccag
ttccgcggccgccgctggaactgcaccaccgtcaacaacagcctggccatcttcggcccc
gtgctggacaaagccacccgggagtccgcctttgtgcatgccattgcctctgccggcgtg
gcctttgccgtgacgcgctcctgtgctgagggctccgccaccatctgtggctgcagcagc
cgccaccagggctccccgggtgagggctggaagtggggcggctgcagcgaggacatcgag
ttcggtggcatggtgtctcgggagtttgcagacgcacgggagaaccggccagatgcccgc
tctgcaatgaaccgccacaacaatgaggctggacgccaggccatcgccagccacatgcac
ctcaagtgcaagtgtcacgggctgtcgggcagctgcgaggtgaagacctgctggtggtcg
cagcccgacttccgcgccattggcgacttcctcaaagacaagtacgacagcgcctcggag
atggtggtggagaagcaccgcgagtcgcgcgggtgggtggagaccctgcggccgcgctac
acctacttcaaggtgcccacggaccgcgacctagtctactacgaggcctcgcccaacttc
tgcgagcccaaccccgagaccggctcattcggtacccgcgaccgcacctgcaacgtgagc
tcgcacggcatcgacggctgcgacctgctgtgctgcggccgcggccacaacgcgcgcacc
gagcggcgccgcgagaagtgccactgcgtcttccactggtgttgctatgtgagctgccag
gagtgctcgcgtgtctacgacgtgcacacctgcaagtag

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