KEGG   Galeopterus variegatus (Sunda flying lemur): 103597576
Entry
103597576         CDS       T08727                                 
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
gvr  Galeopterus variegatus (Sunda flying lemur)
Pathway
gvr04150  mTOR signaling pathway
gvr04310  Wnt signaling pathway
gvr04390  Hippo signaling pathway
gvr04519  Cadherin signaling
gvr04550  Signaling pathways regulating pluripotency of stem cells
gvr04916  Melanogenesis
gvr04934  Cushing syndrome
gvr05010  Alzheimer disease
gvr05022  Pathways of neurodegeneration - multiple diseases
gvr05165  Human papillomavirus infection
gvr05200  Pathways in cancer
gvr05205  Proteoglycans in cancer
gvr05217  Basal cell carcinoma
gvr05224  Breast cancer
gvr05225  Hepatocellular carcinoma
gvr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:gvr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    103597576 (WNT9B)
   04390 Hippo signaling pathway
    103597576 (WNT9B)
   04150 mTOR signaling pathway
    103597576 (WNT9B)
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    103597576 (WNT9B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103597576 (WNT9B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    103597576 (WNT9B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103597576 (WNT9B)
   05205 Proteoglycans in cancer
    103597576 (WNT9B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103597576 (WNT9B)
   05226 Gastric cancer
    103597576 (WNT9B)
   05217 Basal cell carcinoma
    103597576 (WNT9B)
   05224 Breast cancer
    103597576 (WNT9B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103597576 (WNT9B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103597576 (WNT9B)
   05022 Pathways of neurodegeneration - multiple diseases
    103597576 (WNT9B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103597576 (WNT9B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:gvr00536]
    103597576 (WNT9B)
Glycosaminoglycan binding proteins [BR:gvr00536]
 Heparan sulfate / Heparin
  Morphogens
   103597576 (WNT9B)
SSDB
Motif
Pfam: wnt HIF-1a_CTAD
Other DBs
NCBI-GeneID: 103597576
NCBI-ProteinID: XP_008579650
UniProt: A0ABM0RGA9
LinkDB
Position
Unknown
AA seq 196 aa
MAWDYLGSNMMVTSLPYLSLSSLTGREVLTPFPGLGTVAAPVQGRAHLKQCDLLKLSRRQ
KQLCRREPGLAETLRDAAHLGLLECQFQFRHERWNCSLEGRTGLLKRGFKETAFLYAVSS
AALTHVLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGPKRGSK
DLRARADAHNTHVGIK
NT seq 588 nt   +upstreamnt  +downstreamnt
atggcgtgggattacttgggcagcaacatgatggtcaccagtctcccttatctctccctc
tccagcttgaccgggagggaggtcctgacacccttcccagggctgggcacggtggcagcc
ccggtgcagggcagggcccacctgaagcagtgtgacctgctgaagctgtcccgcaggcag
aagcagctatgccggcgggagcctggcctggctgagaccctgcgggacgctgcacatctc
ggcctgcttgagtgccagttccagttccggcatgagcgctggaactgcagcctggagggg
aggacaggtctgctcaagagaggtttcaaggagacggctttcctgtacgcggtgtcctcg
gctgccctcacacatgtcctggcccgggcctgcagcgctgggcgcatggagcgctgcacc
tgcgatgactctccgggcctggagagccggcaggcctggcaatggggtgtgtgtggcgac
aacctcaagtacagcaccaagttcctaagcaacttcctggggcccaagagaggaagcaag
gatctgcgggcacgggcagatgcccacaacacccatgtgggcatcaag

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