KEGG   Piliocolobus tephrosceles (Ugandan red Colobus): 111528375
Entry
111528375         CDS       T07491                                 
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b isoform X1
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
pteh  Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh04150  mTOR signaling pathway
pteh04310  Wnt signaling pathway
pteh04390  Hippo signaling pathway
pteh04550  Signaling pathways regulating pluripotency of stem cells
pteh04916  Melanogenesis
pteh04934  Cushing syndrome
pteh05010  Alzheimer disease
pteh05022  Pathways of neurodegeneration - multiple diseases
pteh05165  Human papillomavirus infection
pteh05200  Pathways in cancer
pteh05205  Proteoglycans in cancer
pteh05217  Basal cell carcinoma
pteh05224  Breast cancer
pteh05225  Hepatocellular carcinoma
pteh05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pteh00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    111528375 (WNT9B)
   04390 Hippo signaling pathway
    111528375 (WNT9B)
   04150 mTOR signaling pathway
    111528375 (WNT9B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    111528375 (WNT9B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    111528375 (WNT9B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    111528375 (WNT9B)
   05205 Proteoglycans in cancer
    111528375 (WNT9B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    111528375 (WNT9B)
   05226 Gastric cancer
    111528375 (WNT9B)
   05217 Basal cell carcinoma
    111528375 (WNT9B)
   05224 Breast cancer
    111528375 (WNT9B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    111528375 (WNT9B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    111528375 (WNT9B)
   05022 Pathways of neurodegeneration - multiple diseases
    111528375 (WNT9B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    111528375 (WNT9B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pteh00536]
    111528375 (WNT9B)
Glycosaminoglycan binding proteins [BR:pteh00536]
 Heparan sulfate / Heparin
  Morphogens
   111528375 (WNT9B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 111528375
NCBI-ProteinID: XP_023050832
Ensembl: ENSPTEG00000022768
UniProt: A0A8C9LQS7
LinkDB
Position
16:54271819..54306802
AA seq 357 aa
MRPPPALALAGLCLLALPAAAASYFGLTGREVLTPFPGLGTAAAPAQGGAHLKQCDLLKL
SRRQKQLCRREPGLAETLRDAAHLGLLECQFQFRHERWNCSLEGRTGLLKRGFKETAFLY
AVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGSK
RGNKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQVLKL
RYDSAVKVSSATNEALGRLELWAPSRQGSPTKGLAPRSGDLVYMEDSPSFCRPSKYSPGT
AGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELVYTCKH
NT seq 1074 nt   +upstreamnt  +downstreamnt
atgcgccccccgcccgcgctggccctggccgggctctgcctgctggcgctgcccgccgcc
gccgcctcctacttcggcctgaccgggcgggaggtcctgacgcccttcccaggactgggc
actgcggcggccccggcacagggcggggcccacctgaagcagtgcgacctgctgaagctg
tcccggcggcagaagcagctctgccggagggagcctggcctggctgagaccctgcgggac
gctgcgcacctcggcctgcttgagtgccagttccagttccggcatgagcgctggaactgt
agcctggagggcaggacgggcctgctcaagagaggcttcaaagagacagctttcctgtat
gcggtgtcctctgccgccctgacccacaccctggcccgggcctgcagcgctgggcgcatg
gagcgctgcacctgtgatgactctccggggctggagagccggcaggcctggcagtggggc
gtgtgtggtgacaacctcaagtacagcaccaagtttctgagcaacttcctggggtccaag
agaggaaacaaggacctgcgggcacgggcagacgcccacaacacccacgtgggcatcaag
gctgtaaagagtggcctcaggacgacgtgtaagtgccacggcgtgtcaggctcctgtgcc
gtgcgcacctgctggaagcagctctccccgttccgtgagacgggccaagtgctgaaactg
cgctatgactcggctgtcaaggtgtccagtgccaccaatgaggccttgggccgcctagag
ctgtgggccccttccaggcagggcagccccaccaaaggcctggccccgaggtctggggac
ctggtctacatggaggactcgcccagcttctgccggcccagcaagtactcgcctggcaca
gcaggtagggtgtgctcccgggaggccagctgcagcagcctgtgctgcgggcggggctat
gacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgctat
gtggagtgccagcaatgtgtgcaggaggagcttgtgtacacctgcaagcactag

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