KEGG   Rousettus aegyptiacus (Egyptian rousette): 107508172
Entry
107508172         CDS       T06036                                 
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
ray  Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04150  mTOR signaling pathway
ray04310  Wnt signaling pathway
ray04390  Hippo signaling pathway
ray04550  Signaling pathways regulating pluripotency of stem cells
ray04916  Melanogenesis
ray04934  Cushing syndrome
ray05010  Alzheimer disease
ray05022  Pathways of neurodegeneration - multiple diseases
ray05165  Human papillomavirus infection
ray05200  Pathways in cancer
ray05205  Proteoglycans in cancer
ray05217  Basal cell carcinoma
ray05224  Breast cancer
ray05225  Hepatocellular carcinoma
ray05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ray00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    107508172 (WNT9B)
   04390 Hippo signaling pathway
    107508172 (WNT9B)
   04150 mTOR signaling pathway
    107508172 (WNT9B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    107508172 (WNT9B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    107508172 (WNT9B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    107508172 (WNT9B)
   05205 Proteoglycans in cancer
    107508172 (WNT9B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    107508172 (WNT9B)
   05226 Gastric cancer
    107508172 (WNT9B)
   05217 Basal cell carcinoma
    107508172 (WNT9B)
   05224 Breast cancer
    107508172 (WNT9B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    107508172 (WNT9B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    107508172 (WNT9B)
   05022 Pathways of neurodegeneration - multiple diseases
    107508172 (WNT9B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    107508172 (WNT9B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ray00536]
    107508172 (WNT9B)
Glycosaminoglycan binding proteins [BR:ray00536]
 Heparan sulfate / Heparin
  Morphogens
   107508172 (WNT9B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 107508172
NCBI-ProteinID: XP_015995308
LinkDB
Position
Unknown
AA seq 358 aa
MRPPPALALAALCLLALPAAAAAAYFGLTGREVLTPFPGLGTVAAPAQDGAHLKQCDLLK
LSRRQKQLCRREPGLADTLRDAAHLSLLECQFQFRLERWNCSLEGRTGLLKRGFKETAFL
YAVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGP
KRGSKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQALK
LRYDSAVKVSSATNEALGRLELWAPAKPGSPTKGLAPRSGDLVYMEDSPSFCRPSKYSPG
TAGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELVYTCKH
NT seq 1077 nt   +upstreamnt  +downstreamnt
atgcgccccccgcccgcgctggccctggccgcgctctgcctgctggcgctgcccgccgcc
gccgctgccgcctacttcggcctgaccgggcgagaagtcctgacgcccttcccagggctg
ggcaccgtggcagccccagcacaggatggggcccacctgaagcagtgtgacctgctgaag
ctgtcccgtcggcagaagcagctctgtcggcgggagcccggcctcgctgacaccctacgg
gatgccgcccacctgagcctgctcgagtgccagttccagttccgcctggagcgctggaac
tgcagcctggaggggaggacgggcctgctcaagagaggttttaaggagacggccttcctg
tacgcggtatcctcggccgccctcacccacactttggcccgggcctgcagtgccggtcgc
atggagcgctgcacctgcgacgactctcccggcctggagagccggcaggcctggcagtgg
ggcgtgtgtggcgacaacctcaagtacagcaccaagttcctgagcaacttcctggggccc
aagagaggaagcaaagacctccgggcgcgggcggacgcccataacacccacgtgggcatc
aaggccgtgaagagtggcctcaggaccacgtgtaagtgccatggcgtatcgggctcctgt
gccgtgcgcacttgctggaagcagctctccccattccgagagaccggccaggccctgaag
ctgcgctacgactcagccgtcaaggtgtccagtgccacgaacgaggccttgggacgccta
gagctgtgggcacctgccaagccaggcagccccaccaagggcctggccccgcggtcaggg
gacctggtctacatggaggactcacccagcttctgccggcccagcaagtactcccctggc
acggcgggcagggtgtgctcccgggaggccagctgcagcagcctgtgctgcgggcggggc
tatgacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgc
tatgtggagtgccagcagtgcgtgcaggaggagctcgtgtacacctgtaagcactag

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