KEGG   Mustela putorius furo (domestic ferret): 101672902
Entry
101672902         CDS       T07239                                 
Symbol
WNT10B
Name
(RefSeq) protein Wnt-10b
  KO
K01357  wingless-type MMTV integration site family, member 10
Organism
mpuf  Mustela putorius furo (domestic ferret)
Pathway
mpuf04150  mTOR signaling pathway
mpuf04310  Wnt signaling pathway
mpuf04390  Hippo signaling pathway
mpuf04550  Signaling pathways regulating pluripotency of stem cells
mpuf04916  Melanogenesis
mpuf04934  Cushing syndrome
mpuf05010  Alzheimer disease
mpuf05022  Pathways of neurodegeneration - multiple diseases
mpuf05165  Human papillomavirus infection
mpuf05200  Pathways in cancer
mpuf05205  Proteoglycans in cancer
mpuf05217  Basal cell carcinoma
mpuf05224  Breast cancer
mpuf05225  Hepatocellular carcinoma
mpuf05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mpuf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101672902 (WNT10B)
   04390 Hippo signaling pathway
    101672902 (WNT10B)
   04150 mTOR signaling pathway
    101672902 (WNT10B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101672902 (WNT10B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    101672902 (WNT10B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101672902 (WNT10B)
   05205 Proteoglycans in cancer
    101672902 (WNT10B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101672902 (WNT10B)
   05226 Gastric cancer
    101672902 (WNT10B)
   05217 Basal cell carcinoma
    101672902 (WNT10B)
   05224 Breast cancer
    101672902 (WNT10B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101672902 (WNT10B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101672902 (WNT10B)
   05022 Pathways of neurodegeneration - multiple diseases
    101672902 (WNT10B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101672902 (WNT10B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mpuf00536]
    101672902 (WNT10B)
Glycosaminoglycan binding proteins [BR:mpuf00536]
 Heparan sulfate / Heparin
  Morphogens
   101672902 (WNT10B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 101672902
NCBI-ProteinID: XP_004778956
Ensembl: ENSMPUG00000014727
UniProt: M3YTF8
LinkDB
Position
Unknown
AA seq 389 aa
MPEEPRPRPPPSGFAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG
LCLRSPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS
FSMLAAGVMHAVATACSLGRLASCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPHSLPSS
GPGLGPSPGPQDTWEWGGCNQDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT
ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAVFIDIHNRNSGAFQPRLR
PRRLSGELVYFEKSPDFCERDPTVGSPGTRGRACNKTSRLLDGCGSLCCGRGHNMLRQTR
VERCHCRFHWCCYVLCDECKVTEWVNVCK
NT seq 1170 nt   +upstreamnt  +downstreamnt
atgccggaggagccccggccgcggcctccgccctcgggctttgcgggtctcctgttcctg
gcgttgtgcagtcgggccctcagcaatgagattctgggcctgaagctgcccggcgagccg
ccgctgaccgccaacaccgtgtgcttgacgctgtcgggcctgagcaagcggcagctgggc
ctctgcctgcgcagccccgacgtgacggcatccgcacttcaaggcctgcacatcgcggtc
cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctccgcgctcgagggcggc
ggccgcctgccgcaccacagcgccatcctcaagcgcggttttcgggagagtgctttttcc
ttctccatgctggcggcaggggtcatgcacgcggtcgcaacggcctgcagcctgggcagg
ctagcgagctgcggctgcggctggaagggcagtggtgagcaggaccggctgagggccaag
ctgctgcagctgcaggctctgtcccggggcaagagtttcccccactccctgcccagctct
ggccccggcttaggtcccagccccggcccccaggacacatgggaatggggtggctgtaac
caggacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc
cgggacatccaggcaagaatgcgaatccacaacaacagggtggggcgacaggtggtaact
gaaaacctgaagcggaaatgcaagtgtcacggcacttcgggcagctgccagttcaagacc
tgctggagggcggccccagagttccgggcggtgggggcagcgctgagggagcggctaggt
cgggccgtcttcatcgatatccacaaccgcaactccggagccttccaaccccgcctgcgt
ccccgtcgcctttcgggagagctggtttactttgagaagtctcccgacttctgtgagcga
gaccctaccgtgggctcccccggcactcggggccgggcatgcaacaagaccagccgtctg
ctggacggctgcggcagcctgtgctgcggccgtgggcacaatatgcttcggcagactcga
gttgagcgctgtcattgccgcttccattggtgctgctacgtgctgtgcgacgagtgcaaa
gtcacagagtgggttaacgtgtgtaagtga

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