KEGG   Panthera pardus (leopard): 109249054
Entry
109249054         CDS       T06062                                 
Symbol
WNT10B
Name
(RefSeq) protein Wnt-10b
  KO
K01357  wingless-type MMTV integration site family, member 10
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
    109249054 (WNT10B)
   04390 Hippo signaling pathway
    109249054 (WNT10B)
   04150 mTOR signaling pathway
    109249054 (WNT10B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    109249054 (WNT10B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    109249054 (WNT10B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    109249054 (WNT10B)
   05205 Proteoglycans in cancer
    109249054 (WNT10B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    109249054 (WNT10B)
   05226 Gastric cancer
    109249054 (WNT10B)
   05217 Basal cell carcinoma
    109249054 (WNT10B)
   05224 Breast cancer
    109249054 (WNT10B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    109249054 (WNT10B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    109249054 (WNT10B)
   05022 Pathways of neurodegeneration - multiple diseases
    109249054 (WNT10B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    109249054 (WNT10B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ppad00536]
    109249054 (WNT10B)
Glycosaminoglycan binding proteins [BR:ppad00536]
 Heparan sulfate / Heparin
  Morphogens
   109249054 (WNT10B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 109249054
NCBI-ProteinID: XP_019274764
Ensembl: ENSPPRG00000011632
UniProt: A0A9V1E5U9
LinkDB
Position
Unknown
AA seq 389 aa
MPEEPRPRPPPSGFAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG
LCLRSPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS
FSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPHSLPSP
GPGSGPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT
ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLR
PRRLSGELVYFEKSPDFCERDPAVGSPGTRGRACNKTSRLLDGCGSLCCGRGHNLLRQTR
VERCHCRFHWCCYVLCDECKVTEWVNVCK
NT seq 1170 nt   +upstreamnt  +downstreamnt
atgccggaggagccccggccgcgccctccgccctcgggcttcgcgggtctcctgtttctg
gcgttgtgcagtcgggccctcagcaatgagattctgggcctgaagctgcccggcgagccg
ccgctgaccgccaacaccgtatgcttgacgctgtcgggcctgagcaaacggcagctaggc
ctgtgcctgcgcagccccgacgtgacggcatccgcgcttcagggcctgcatatcgcggtc
cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctcggcgctggagggcggc
ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgggagagtgctttttcc
ttctccatgctggctgcaggggtcatgcacgcggtagccacggcctgcagcctgggcaag
ctggtgagctgcggctgcggctggaagggcagtggtgagcaggatcggctgagggccaaa
ctactgcagctgcaggcactgtcccggggcaagagtttcccccactccctgcccagtcct
ggccctggctcaggccccagccctggcccccaggacacatgggaatggggtggctgtaac
catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc
cgggacatccaggcaagaatgcgaatccacaacaacagggtggggcgacaggtggtgact
gaaaacctgaagcggaaatgcaagtgccatggcacgtcaggcagttgccagttcaagacc
tgctggagggcggccccagagttccgggcagtgggggcggcgttgagggagcggctgggt
cgggccatcttcatcgatacccacaaccgcaactccggagccttccagccccgcctgcgt
ccccgtcgcctctcaggagagctggtctactttgagaagtcgcctgacttctgtgagcga
gaccctgccgtgggctccccgggcactcggggccgggcctgcaataagaccagccgcctg
ctggatggctgtggcagcctgtgctgtggccgtgggcacaacctgctccggcagacacga
gtcgagcgctgtcattgccgcttccactggtgctgctacgtgctgtgtgatgagtgcaag
gtcacagagtgggtcaacgtgtgtaagtga

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