KEGG   Nomascus leucogenys (northern white-cheeked gibbon): 100602760
Entry
100602760         CDS       T03265                                 
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b isoform X1
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
nle  Nomascus leucogenys (northern white-cheeked gibbon)
Pathway
nle04150  mTOR signaling pathway
nle04310  Wnt signaling pathway
nle04390  Hippo signaling pathway
nle04550  Signaling pathways regulating pluripotency of stem cells
nle04916  Melanogenesis
nle04934  Cushing syndrome
nle05010  Alzheimer disease
nle05022  Pathways of neurodegeneration - multiple diseases
nle05165  Human papillomavirus infection
nle05200  Pathways in cancer
nle05205  Proteoglycans in cancer
nle05217  Basal cell carcinoma
nle05224  Breast cancer
nle05225  Hepatocellular carcinoma
nle05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:nle00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100602760 (WNT9B)
   04390 Hippo signaling pathway
    100602760 (WNT9B)
   04150 mTOR signaling pathway
    100602760 (WNT9B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100602760 (WNT9B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100602760 (WNT9B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100602760 (WNT9B)
   05205 Proteoglycans in cancer
    100602760 (WNT9B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100602760 (WNT9B)
   05226 Gastric cancer
    100602760 (WNT9B)
   05217 Basal cell carcinoma
    100602760 (WNT9B)
   05224 Breast cancer
    100602760 (WNT9B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100602760 (WNT9B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100602760 (WNT9B)
   05022 Pathways of neurodegeneration - multiple diseases
    100602760 (WNT9B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100602760 (WNT9B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:nle00536]
    100602760 (WNT9B)
Glycosaminoglycan binding proteins [BR:nle00536]
 Heparan sulfate / Heparin
  Morphogens
   100602760 (WNT9B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100602760
NCBI-ProteinID: XP_030655766
Position
19:30445250..30480307
AA seq 358 aa
MRPPPALALAGLCLLALPTAAAASYFGLTGREVLTPFPGLGTAAAPAEGGAHLKQCDLLK
LSRRQKQLCRREPGLAETLRDAAHLGLLECQFQFRHERWNCSLEGRTGLLKRGFKETAFL
YAVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGS
KRGNKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQVLK
LRYDSAVKVSSATNEALGRLELWAPARQGSLTKGLAPRSGDLVYMEDSPSFCRPSKYSPG
TAGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELVYTCKH
NT seq 1077 nt   +upstreamnt  +downstreamnt
atgcgccccccgcccgcgctggccctggccgggctctgcctgctggcgctgcccaccgcc
gccgccgcctcctacttcggcctgaccgggcgggaagtcctgacgcccttcccaggattg
ggcactgcggcggccccggcagagggcggggcccacctgaagcagtgcgacctgctgaag
ctctcccggcggcagaagcagctctgccggagggagcccggcctggctgagaccctgagg
gacgctgcgcacctcggcctgcttgagtgccagtttcagttccggcatgagcgctggaac
tgtagcctggagggcaggacaggcctgctcaagagaggcttcaaagagacagctttcctg
tacgcagtgtcctctgccgccctcacccacaccctggcccgggcctgcagtgctgggcgc
atggagcgctgcacctgtgatgactctccagggctggagagccggcaggcctggcagtgg
ggtgtgtgcggtgacaacctcaagtacagcaccaagtttctgagcaacttcctggggtcc
aagagaggcaacaaggacctgcgggcacgggcagacgcccacaacacccacgtgggcatc
aaggctgtgaagagtggcctcaggaccacgtgtaagtgccatggcgtatcaggctcctgt
gccgtgcgcacctgctggaagcagctctccccattccgtgagacgggccaggtgctgaaa
ctgcgctatgactcggctgtcaaggtgtccagcgccaccaatgaggccttgggccgccta
gagctgtgggcccctgccaggcagggcagcctcaccaaaggcctggccccgaggtctggg
gacctggtctacatggaggactcacccagcttctgccggcccagcaagtactcgcctggc
acagcgggtagggtgtgctcccgggaagccagctgcagcagcctgtgctgcgggcggggc
tatgacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgc
tacgtggagtgccagcaatgtgtgcaggaggagcttgtgtacacctgcaagcactag

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