KEGG   Panthera pardus (leopard): 109259736
Entry
109259736         CDS       T06062                                 
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
ppad  Panthera pardus (leopard)
Pathway
ppad04150  mTOR signaling pathway
ppad04310  Wnt signaling pathway
ppad04390  Hippo signaling pathway
ppad04550  Signaling pathways regulating pluripotency of stem cells
ppad04916  Melanogenesis
ppad04934  Cushing syndrome
ppad05010  Alzheimer disease
ppad05022  Pathways of neurodegeneration - multiple diseases
ppad05165  Human papillomavirus infection
ppad05200  Pathways in cancer
ppad05205  Proteoglycans in cancer
ppad05217  Basal cell carcinoma
ppad05224  Breast cancer
ppad05225  Hepatocellular carcinoma
ppad05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ppad00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    109259736 (WNT9B)
   04390 Hippo signaling pathway
    109259736 (WNT9B)
   04150 mTOR signaling pathway
    109259736 (WNT9B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    109259736 (WNT9B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    109259736 (WNT9B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    109259736 (WNT9B)
   05205 Proteoglycans in cancer
    109259736 (WNT9B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    109259736 (WNT9B)
   05226 Gastric cancer
    109259736 (WNT9B)
   05217 Basal cell carcinoma
    109259736 (WNT9B)
   05224 Breast cancer
    109259736 (WNT9B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    109259736 (WNT9B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    109259736 (WNT9B)
   05022 Pathways of neurodegeneration - multiple diseases
    109259736 (WNT9B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    109259736 (WNT9B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ppad00536]
    109259736 (WNT9B)
Glycosaminoglycan binding proteins [BR:ppad00536]
 Heparan sulfate / Heparin
  Morphogens
   109259736 (WNT9B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 109259736
NCBI-ProteinID: XP_019293008
LinkDB
Position
Unknown
AA seq 373 aa
MERTVVAKTGYPEGRDPPATAVAGPESRTVQGSLAPSFALSSLTGREVLTPFPGLGTAAA
PAQSGVHLKPCDLLKLSRRQKQLCRREPGLAETLQDAAHLSLLECQFQFRHERWNCSLEG
RTGLLKRGFKETAFLYAMSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGD
NLKYSTKFLSNFLGPKRGSKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTC
WKQLAPFRETGQALKLRYDSAVKVSSATNEALGRLELWAPARPGSPTKGPAPRPGDLVYM
EDSPSFCRPSKYSPGTAGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQ
QCVQEELIYTCKH
NT seq 1122 nt   +upstreamnt  +downstreamnt
atggagcggactgtggtagccaagactggctaccctgaggggagggacccccctgctaca
gccgtggctggccctgagtccagaacagtccaagggtcactagctccctcttttgctctc
tctagcctgaccgggcgggaggtcctgacgcccttcccagggctgggcactgctgcggcc
ccagcacagagcggggtccacctgaagccgtgtgacctgctgaagctgtcccgccgacag
aaacagctctgccggagggagcccggcctggccgagaccctgcaggacgctgctcacctc
agcctgctcgagtgccagtttcagttccgacatgagcgttggaactgcagtctggagggg
aggacaggcctgctcaagagaggtttcaaggagacggccttcctgtatgcaatgtcctcc
gctgccctcacccacactctggcccgggcctgcagcgccgggcgcatggagcgctgcacc
tgtgatgattctccgggcctggagagccggcaggcctggcagtggggcgtgtgcggcgac
aacctcaagtacagcaccaagttcctgagcaacttcctggggcccaagagaggaagcaaa
gacctgagggcacgggcagacgctcacaacacccacgtgggcatcaaggcagtgaagagt
ggcctcaggaccacatgtaagtgccacggtgtgtcgggctcctgtgccgtgcgcacctgc
tggaaacagctcgccccgttccgtgagacgggccaggcgctaaaactgcgttatgactca
gctgtcaaggtgtccagtgccaccaacgaggccttgggccgcctggagctgtgggcgccc
gcccggccaggcagccccaccaagggcccggccccgcggcccggggacctggtctatatg
gaagactcgcccagtttctgccggcccagcaagtactcgcccggcacggcgggcagggtg
tgttcccgggaggccagctgcagcagcctgtgctgcggccggggctacgacacccagagc
cgcctggtggccttctcctgccactgccaggtgcagtggtgctgctacgtggagtgccag
cagtgcgtgcaggaggagctcatatacacctgcaagcattag

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