KEGG   Macaca fascicularis (crab-eating macaque): 102130297
Entry
102130297         CDS       T02918                                 
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
mcf  Macaca fascicularis (crab-eating macaque)
Pathway
mcf04150  mTOR signaling pathway
mcf04310  Wnt signaling pathway
mcf04390  Hippo signaling pathway
mcf04550  Signaling pathways regulating pluripotency of stem cells
mcf04916  Melanogenesis
mcf04934  Cushing syndrome
mcf05010  Alzheimer disease
mcf05022  Pathways of neurodegeneration - multiple diseases
mcf05165  Human papillomavirus infection
mcf05200  Pathways in cancer
mcf05205  Proteoglycans in cancer
mcf05217  Basal cell carcinoma
mcf05224  Breast cancer
mcf05225  Hepatocellular carcinoma
mcf05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mcf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102130297 (WNT9B)
   04390 Hippo signaling pathway
    102130297 (WNT9B)
   04150 mTOR signaling pathway
    102130297 (WNT9B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102130297 (WNT9B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102130297 (WNT9B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102130297 (WNT9B)
   05205 Proteoglycans in cancer
    102130297 (WNT9B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102130297 (WNT9B)
   05226 Gastric cancer
    102130297 (WNT9B)
   05217 Basal cell carcinoma
    102130297 (WNT9B)
   05224 Breast cancer
    102130297 (WNT9B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102130297 (WNT9B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102130297 (WNT9B)
   05022 Pathways of neurodegeneration - multiple diseases
    102130297 (WNT9B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102130297 (WNT9B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mcf00536]
    102130297 (WNT9B)
Glycosaminoglycan binding proteins [BR:mcf00536]
 Heparan sulfate / Heparin
  Morphogens
   102130297 (WNT9B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 102130297
NCBI-ProteinID: XP_045231819
Ensembl: ENSMFAG00000040531
LinkDB
Position
16:complement(join(66901447..66901920,66903320..66903585,66905892..66906148,66928233..66928309))
AA seq 357 aa
MRPPPALALAGLCLLALPAAAASYFGLTGREVLTPFPGLGTAAAPAQGGAHLKQCDLLKL
SRRQKQLCRREPGLAETLRDAAHLGLLECQFQFRHERWNCSLEGRTGLLKRGFKETAFLY
AVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGSK
RGNKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQVLKL
RYDSAVKVSSATNEALGRLELWAPSRQGSPTKGLAPRSGDLVYMEDSPSFCRPSKYSPGT
AGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELVYTCKH
NT seq 1074 nt   +upstreamnt  +downstreamnt
atgcgccccccgccagcgctggccctggccgggctctgcctgctggcgctgcccgccgcc
gccgcctcctacttcggcctgaccgggcgggaggtcctgacgcccttcccaggactgggc
actgcagcggccccggcacagggcggggcccacctgaagcagtgcgacctgctgaagctg
tcccggcggcagaagcagctctgccggagggagcctggcctggctgagaccctgcgggac
gctgcgcacctcggcctgcttgagtgccagttccagttccggcatgagcgctggaactgt
agcctggagggcaggacgggcctgctcaagagaggcttcaaagagacagctttcctgtat
gcggtgtcctctgccgccctaacccacaccctggcccgggcctgcagcgctgggcgcatg
gagcgctgcacctgtgatgactctccggggctggagagccggcaggcctggcagtggggc
gtgtgtggtgacaacctcaagtacagcaccaagtttctgagcaacttcctggggtccaag
agaggaaacaaggacctgcgggcacgggcagacgcccacaacacccacgtgggcatcaag
gctgtgaagagtggcctcaggacgacgtgtaagtgccacggcgtgtcaggctcctgtgcc
gtgcgcacctgctggaagcagctctccccattccgtgagacgggccaggtgctgaaactg
cgctatgactcggctgtcaaggtgtccagtgccaccaatgaggccttgggccgcctagag
ctgtgggccccttccaggcagggcagccccaccaaaggcctggccccaaggtctggggac
ctggtctacatggaggactcgcccagcttctgtcgacccagcaagtactcgcctggcacg
gcaggtagggtgtgctcccgggaggccagctgcagcagcctgtgctgcgggcggggctat
gacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgctac
gtggagtgccagcaatgtgtgcaggaggagcttgtgtacacctgcaagcactag

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