KEGG   Phodopus roborovskii (desert hamster): 127219219
Entry
127219219         CDS       T08852                                 
Symbol
Wnt3a
Name
(RefSeq) protein Wnt-3a
  KO
K00312  wingless-type MMTV integration site family, member 3
Organism
prob  Phodopus roborovskii (desert hamster)
Pathway
prob04150  mTOR signaling pathway
prob04310  Wnt signaling pathway
prob04390  Hippo signaling pathway
prob04550  Signaling pathways regulating pluripotency of stem cells
prob04916  Melanogenesis
prob04934  Cushing syndrome
prob05010  Alzheimer disease
prob05022  Pathways of neurodegeneration - multiple diseases
prob05165  Human papillomavirus infection
prob05200  Pathways in cancer
prob05205  Proteoglycans in cancer
prob05206  MicroRNAs in cancer
prob05217  Basal cell carcinoma
prob05224  Breast cancer
prob05225  Hepatocellular carcinoma
prob05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:prob00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    127219219 (Wnt3a)
   04390 Hippo signaling pathway
    127219219 (Wnt3a)
   04150 mTOR signaling pathway
    127219219 (Wnt3a)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    127219219 (Wnt3a)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    127219219 (Wnt3a)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    127219219 (Wnt3a)
   05206 MicroRNAs in cancer
    127219219 (Wnt3a)
   05205 Proteoglycans in cancer
    127219219 (Wnt3a)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    127219219 (Wnt3a)
   05226 Gastric cancer
    127219219 (Wnt3a)
   05217 Basal cell carcinoma
    127219219 (Wnt3a)
   05224 Breast cancer
    127219219 (Wnt3a)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    127219219 (Wnt3a)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    127219219 (Wnt3a)
   05022 Pathways of neurodegeneration - multiple diseases
    127219219 (Wnt3a)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    127219219 (Wnt3a)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:prob00536]
    127219219 (Wnt3a)
Glycosaminoglycan binding proteins [BR:prob00536]
 Heparan sulfate / Heparin
  Morphogens
   127219219 (Wnt3a)
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 127219219
NCBI-ProteinID: XP_051036520
LinkDB
Position
Unknown
AA seq 352 aa
MAPLGYLLVLCSLKQALGSYPIWWSLAVGPQYSSLSTQPILCASIPGLVPKQLRFCRNYV
EIMPSVAEGVKAGIQECQHQFRGRRWNCTTVSNSLAIFGPVLDKATRESAFVHAIASAGV
AFAVTRSCAEGSAAICGCSSRLQGSPGEGWKWGGCSEDIEFGGMVSREFADARENRPDAR
SAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRTVGDFLKDKYDSASE
MVVEKHRESRGWVETLRPRYTYFKVPTERDLVYYEASPNFCEPNPETGSFGTRDRTCNVS
SHGIDGCDLLCCGRGHNARTERRREKCHCVFHWCCYVSCQECTRVYDVHTCK
NT seq 1059 nt   +upstreamnt  +downstreamnt
atggctcctctcggatacctcttagtgctctgcagcctgaagcaggcgctgggtagctac
ccgatctggtggtctttggctgtgggacctcagtactcctctctgagcactcagcccatc
ctctgtgccagcatcccaggcctggtgcccaagcagctgcgcttctgcaggaactatgta
gagatcatgcccagcgtggctgaaggtgtcaaggctggcatccaggagtgccagcaccag
ttccgaggccggcgttggaactgtaccactgtcagcaacagcctggcaatctttggccct
gttctggacaaagccactcgggagtcagcctttgtccatgccattgcctctgctggagtg
gcctttgcagtgacccgctcatgtgcagagggttcagctgccatctgtgggtgcagtagc
cgcctccagggttccccaggcgagggctggaagtggggcggttgtagcgaggacattgaa
tttggcggaatggtgtctcgggagtttgctgatgccagggagaaccggccagatgcccgc
tctgccatgaaccgtcataacaatgaggctgggcgccaggccatcgctagtcacatgcac
ctcaagtgtaaatgccacggactatcgggcagctgtgaagtgaagacctgctggtggtcg
cagcccgacttccgcactgtcggggatttcctcaaagacaagtatgacagcgcctccgag
atggtggtggagaaacaccgtgagtctcgtggctgggtggagaccctgagaccacgttac
acgtacttcaaggtgcccacagagcgcgacctggtctactacgaggcctcgcccaacttc
tgtgagccgaaccctgaaaccggctcctttgggacacgcgaccgcacctgcaacgtgagc
tcgcatggcatagatgggtgtgacctgctgtgctgcgggcgtggccataatgcacgcact
gagcgacgaagggagaagtgccactgtgttttccactggtgctgctacgtcagttgtcag
gagtgcacacgcgtctatgatgtgcacacctgcaagtag

DBGET integrated database retrieval system