KEGG   Pipistrellus kuhlii (Kuhl's pipistrelle): 118726528
Entry
118726528         CDS       T07682                                 
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
pkl  Pipistrellus kuhlii (Kuhl's pipistrelle)
Pathway
pkl04150  mTOR signaling pathway
pkl04310  Wnt signaling pathway
pkl04390  Hippo signaling pathway
pkl04519  Cadherin signaling
pkl04550  Signaling pathways regulating pluripotency of stem cells
pkl04916  Melanogenesis
pkl04934  Cushing syndrome
pkl05010  Alzheimer disease
pkl05022  Pathways of neurodegeneration - multiple diseases
pkl05165  Human papillomavirus infection
pkl05200  Pathways in cancer
pkl05205  Proteoglycans in cancer
pkl05217  Basal cell carcinoma
pkl05224  Breast cancer
pkl05225  Hepatocellular carcinoma
pkl05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pkl00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    118726528 (WNT9B)
   04390 Hippo signaling pathway
    118726528 (WNT9B)
   04150 mTOR signaling pathway
    118726528 (WNT9B)
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    118726528 (WNT9B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    118726528 (WNT9B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    118726528 (WNT9B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    118726528 (WNT9B)
   05205 Proteoglycans in cancer
    118726528 (WNT9B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    118726528 (WNT9B)
   05226 Gastric cancer
    118726528 (WNT9B)
   05217 Basal cell carcinoma
    118726528 (WNT9B)
   05224 Breast cancer
    118726528 (WNT9B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    118726528 (WNT9B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    118726528 (WNT9B)
   05022 Pathways of neurodegeneration - multiple diseases
    118726528 (WNT9B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    118726528 (WNT9B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pkl00536]
    118726528 (WNT9B)
Glycosaminoglycan binding proteins [BR:pkl00536]
 Heparan sulfate / Heparin
  Morphogens
   118726528 (WNT9B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 118726528
NCBI-ProteinID: XP_036307317
LinkDB
Position
Unknown
AA seq 357 aa
MRPAPPPALAALLLLALPAAHAAYFGLTGREVLTPFAGLGTAAAPAQGGAHLKQCDLLKL
SRRQKQLCRREPGLAETLQDAAHLSLLECQFQFRQERWNCSLEGRTGLLKRGFKETAFLY
AVSAAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGPK
RGSKDLRARADAHNTNVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQALKL
RYDSAVKVSSATNEALGRLELWAPARLDGPAKGLAPRPGDLVYMEDSPSFCQPSKYSPGT
AGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELLYTCKP
NT seq 1074 nt   +upstreamnt  +downstreamnt
atgcgccccgcgccgcccccggccctggccgcgctcctcctgctggcgctgcccgccgcc
cacgccgcctacttcggcctgactggccgggaggtcctgacgcccttcgccgggctgggc
accgcggcggcgccggcccagggcggggcccacctgaagcagtgcgacctgctgaagctg
tcccggcggcagaagcagctctgccggcgggaacccggcctggccgagaccctgcaggat
gctgcccacctcagcctgctggagtgccagttccagtttcggcaggagcgctggaactgc
agcctggaggggaggaccggcctgctcaagagaggcttcaaggagacggccttcctgtac
gcggtgtcagcggccgccctcacgcacacgctggcgcgggcctgcagcgccggccgcatg
gagcgctgcacctgcgacgactccccgggcctggagagccggcaggcctggcagtggggc
gtgtgcggcgacaacctcaagtacagcaccaagttcctgagcaacttcctggggcccaag
agggggagcaaggacctgcgggcgcgggccgacgcccacaacaccaacgtgggcatcaag
gccgtcaagagtggcctcaggaccacctgcaagtgccacggcgtgtccggctcctgcgcc
gtgcgcacctgctggaagcagctctccccgttccgggagacgggccaggcgctcaagctg
cgctacgactcggccgtcaaggtgtccagcgccaccaacgaggccctgggccgcctggag
ctgtgggcgcccgccaggctggacggtcccgccaagggcctggccccccggccgggggac
ctggtctacatggaggactcgcccagcttctgccagcccagcaagtactccccgggcacg
gcgggcagggtgtgctcccgggaggccagctgcagcagcctgtgctgcgggcggggctac
gacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgctac
gtggagtgccagcagtgcgtgcaggaggagctcctgtacacctgcaagccctag

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