KEGG   Pteropus alecto (black flying fox): 102895795
Entry
102895795         CDS       T02993                                 
Symbol
WNT3A
Name
(RefSeq) protein Wnt-3a
  KO
K00312  wingless-type MMTV integration site family, member 3
Organism
pale  Pteropus alecto (black flying fox)
Pathway
pale04150  mTOR signaling pathway
pale04310  Wnt signaling pathway
pale04390  Hippo signaling pathway
pale04550  Signaling pathways regulating pluripotency of stem cells
pale04916  Melanogenesis
pale04934  Cushing syndrome
pale05010  Alzheimer disease
pale05022  Pathways of neurodegeneration - multiple diseases
pale05165  Human papillomavirus infection
pale05200  Pathways in cancer
pale05205  Proteoglycans in cancer
pale05206  MicroRNAs in cancer
pale05217  Basal cell carcinoma
pale05224  Breast cancer
pale05225  Hepatocellular carcinoma
pale05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pale00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102895795 (WNT3A)
   04390 Hippo signaling pathway
    102895795 (WNT3A)
   04150 mTOR signaling pathway
    102895795 (WNT3A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102895795 (WNT3A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102895795 (WNT3A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102895795 (WNT3A)
   05206 MicroRNAs in cancer
    102895795 (WNT3A)
   05205 Proteoglycans in cancer
    102895795 (WNT3A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102895795 (WNT3A)
   05226 Gastric cancer
    102895795 (WNT3A)
   05217 Basal cell carcinoma
    102895795 (WNT3A)
   05224 Breast cancer
    102895795 (WNT3A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102895795 (WNT3A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102895795 (WNT3A)
   05022 Pathways of neurodegeneration - multiple diseases
    102895795 (WNT3A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102895795 (WNT3A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pale00536]
    102895795 (WNT3A)
Glycosaminoglycan binding proteins [BR:pale00536]
 Heparan sulfate / Heparin
  Morphogens
   102895795 (WNT3A)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 102895795
NCBI-ProteinID: XP_006923326
LinkDB
Position
Unknown
AA seq 352 aa
MALLRYFLFLYGLKQALGSYPIWWSLAVGPQYSSLGMQPILCASIPGLVPKQLRFCRNYV
EIMPSVAEGLRVSIQECQHQFRGRRWNCTTVNNSLAIFGPVLDKATRESAFVHAIAAAGV
AFAVTRSCAEGSATICGCSSRHQSSPGDGWKWGGCSEDIEFGGMVSREFADARENRPDAR
SAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRAIGDLLKDKYDSASE
MVVEKHRESRGWVETLRPRYTYFKVPTERDLVYYEASPNFCEPNPETGSFGTRDRTCNVS
SPGIDGCDLLCCGRGHNARAERRREKCHCVFHWCCYVSCQECARVYDVHTCK
NT seq 1059 nt   +upstreamnt  +downstreamnt
atggccctgctccggtacttcttattcctctacggcctgaagcaggcgctgggcagctac
ccgatctggtggtccctggctgttgggccccagtattcatctctgggcatgcagcccatc
ctctgtgccagcatcccgggcctggtccccaagcagctgcgcttctgccggaactacgtc
gagatcatgcccagcgtggcagaaggcctccgggtcagcatccaggagtgccagcaccag
ttccgcggtcgccggtggaactgtaccaccgtcaacaacagcctggccatcttcggcccc
gtgctggacaaagccacccgggaatctgcctttgtgcacgccatcgctgccgctggcgtg
gccttcgcggtgacgcgctcctgcgcggagggctccgccaccatctgcggctgcagcagc
cgccaccagagctcaccgggagacggctggaagtggggcggctgcagcgaggacatcgag
ttcggcgggatggtgtctcgggagttcgcggatgcacgggagaacaggcctgacgcccgc
tctgcaatgaaccgccataacaacgaggcggggcgccaggccatcgccagccacatgcac
ctcaagtgcaagtgccacgggctgtcgggcagctgcgaggtgaagacttgctggtggtcg
cagcccgacttccgcgccatcggcgacctcctcaaggacaagtacgacagcgcctcggaa
atggtagtggagaagcaccgcgagtcccgcggctgggtggagacgctgcggccgcgctac
acctacttcaaggtgcccacggagcgcgacctggtctactacgaggcctcgcccaacttc
tgcgagcccaaccccgagaccggctcattcggcacgcgcgaccgcacctgcaacgtgagc
tcgccgggcattgacggctgcgatttgctgtgctgtggccgcggccacaacgcgcgcgcg
gagcggcgccgggagaagtgccactgcgtctttcactggtgctgctacgtgagctgccag
gagtgcgcgcgcgtctacgatgtgcacacctgcaagtag

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