KEGG   Trachypithecus francoisi (Francois's langur): 117067211
Entry
117067211         CDS       T07225                                 
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
tfn  Trachypithecus francoisi (Francois's langur)
Pathway
tfn04150  mTOR signaling pathway
tfn04310  Wnt signaling pathway
tfn04390  Hippo signaling pathway
tfn04550  Signaling pathways regulating pluripotency of stem cells
tfn04916  Melanogenesis
tfn04934  Cushing syndrome
tfn05010  Alzheimer disease
tfn05022  Pathways of neurodegeneration - multiple diseases
tfn05165  Human papillomavirus infection
tfn05200  Pathways in cancer
tfn05205  Proteoglycans in cancer
tfn05217  Basal cell carcinoma
tfn05224  Breast cancer
tfn05225  Hepatocellular carcinoma
tfn05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:tfn00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    117067211 (WNT9B)
   04390 Hippo signaling pathway
    117067211 (WNT9B)
   04150 mTOR signaling pathway
    117067211 (WNT9B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    117067211 (WNT9B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    117067211 (WNT9B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    117067211 (WNT9B)
   05205 Proteoglycans in cancer
    117067211 (WNT9B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    117067211 (WNT9B)
   05226 Gastric cancer
    117067211 (WNT9B)
   05217 Basal cell carcinoma
    117067211 (WNT9B)
   05224 Breast cancer
    117067211 (WNT9B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    117067211 (WNT9B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    117067211 (WNT9B)
   05022 Pathways of neurodegeneration - multiple diseases
    117067211 (WNT9B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    117067211 (WNT9B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:tfn00536]
    117067211 (WNT9B)
Glycosaminoglycan binding proteins [BR:tfn00536]
 Heparan sulfate / Heparin
  Morphogens
   117067211 (WNT9B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 117067211
NCBI-ProteinID: XP_033039385
LinkDB
Position
Unknown
AA seq 330 aa
MRPPPALALAGLCLLALPAAAAASYFGLTGREVLTPFPGLGTAAAPAQGGAHLKQCDLLK
LSRRQKQLCRREPGLAETLRDAAHLGLLECQFQFRHERWNCSLEGRTGLLKRGFKETAFL
YAVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGS
KRGNKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQVLK
LRYDSAVKVSSATNEALGRLELWAPSRQGSPTKGLAPRSGDLVYMEDSPSFCRPSKYSPG
TAGRSAVARSRLTATSTSQIRAILLSQPPE
NT seq 993 nt   +upstreamnt  +downstreamnt
atgcgccccccgcccgcgctggccctggccgggctctgcctgctggcgctgcccgccgcc
gccgccgcctcctacttcggcctgactgggcgggaggtcctgacgcccttcccaggactg
ggcactgcggcggccccagcacagggcggggcccacctgaagcagtgcgacctgctgaag
ctgtcccggcggcagaagcagctctgccggagggagcctggcctggctgagaccctgcgg
gacgctgcgcacctcggcctgcttgagtgccagttccagttccggcatgagcgctggaac
tgtagcctggagggcaggacgggcctgctcaagagaggcttcaaagagacagctttcctg
tatgcggtgtcctctgccgccctaacccacaccctggcccgggcctgcagcgctgggcgc
atggagcgctgcacctgtgatgactctccagggctggagagccggcaggcctggcagtgg
ggcgtgtgtggtgacaacctcaagtacagcaccaagtttctgagcaacttcctggggtcc
aagagaggaaacaaggacctgcgggcacgggcagatgcccacaacacccacgtgggcatc
aaggctgtaaagagtggcctcaggacgacgtgtaagtgccacggcgtgtcaggctcctgt
gccgtgcgcacctgctggaagcagctctccccgttccgtgagacgggtcaagtgctgaaa
ctgcgctatgactcggctgtcaaggtgtccagtgccaccaatgaggccttgggccgccta
gagctgtgggccccttccaggcagggcagccccaccaaaggcctggccccgaggtctggg
gacctggtctacatggaggactcgcccagcttctgccgtcccagcaagtactcgcctggc
acggcaggtaggagtgcagtggcaagatctcggctcaccgcaacctccacctcccagatt
cgagcgattctcctgtctcagccgcctgagtag

DBGET integrated database retrieval system