KEGG   Bison bison bison (American bison): 105001684
Entry
105001684         CDS       T08726                                 
Symbol
WNT10B
Name
(RefSeq) protein Wnt-10b
  KO
K01357  wingless-type MMTV integration site family, member 10
Organism
bbis  Bison bison bison (American bison)
Pathway
bbis04150  mTOR signaling pathway
bbis04310  Wnt signaling pathway
bbis04390  Hippo signaling pathway
bbis04550  Signaling pathways regulating pluripotency of stem cells
bbis04916  Melanogenesis
bbis04934  Cushing syndrome
bbis05010  Alzheimer disease
bbis05022  Pathways of neurodegeneration - multiple diseases
bbis05165  Human papillomavirus infection
bbis05200  Pathways in cancer
bbis05205  Proteoglycans in cancer
bbis05217  Basal cell carcinoma
bbis05224  Breast cancer
bbis05225  Hepatocellular carcinoma
bbis05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:bbis00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105001684 (WNT10B)
   04390 Hippo signaling pathway
    105001684 (WNT10B)
   04150 mTOR signaling pathway
    105001684 (WNT10B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105001684 (WNT10B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105001684 (WNT10B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105001684 (WNT10B)
   05205 Proteoglycans in cancer
    105001684 (WNT10B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105001684 (WNT10B)
   05226 Gastric cancer
    105001684 (WNT10B)
   05217 Basal cell carcinoma
    105001684 (WNT10B)
   05224 Breast cancer
    105001684 (WNT10B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105001684 (WNT10B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105001684 (WNT10B)
   05022 Pathways of neurodegeneration - multiple diseases
    105001684 (WNT10B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105001684 (WNT10B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:bbis00536]
    105001684 (WNT10B)
Glycosaminoglycan binding proteins [BR:bbis00536]
 Heparan sulfate / Heparin
  Morphogens
   105001684 (WNT10B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 105001684
NCBI-ProteinID: XP_010856364
UniProt: A0A6P3IVW2
LinkDB
Position
Unknown
AA seq 369 aa
MREEPRPRPPPSGLAGLLFLALCSRALGNEIQGLKLPGGGEPPLTEQKLGTKTPMALKPG
SIPLLSAVGAPGGSHLSSGLSDLPLSTPLSSPGFRESAFSFSMLAAGVMHAVATACSLGK
LVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFSHSLPSSGPGSGPSPGPQDTWEWGGCN
HDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVTENLKRKCKCHGTSGSCQLKT
CWRAPPEFRAVGAALRERLDRAIFIDTHNRNSGAFQPRLRPRRLSGELVYFENSPDFCER
DPTVGSPGTQGRACNKTSHQLGSCGSLCCGRGHNVLRQTRVERCNCRFHWCCYVLCDECK
VTEWVNVCK
NT seq 1110 nt   +upstreamnt  +downstreamnt
atgcgggaggagccccggccgcggcctccgccctcgggcctcgccggtctcctgttcctg
gcgttgtgcagtcgggccctcggcaatgagattcagggcttgaagctgccgggcggcggc
gagccgccgctgaccgagcagaagctgggaacaaagaccccgatggctttgaagccgggg
agcatccccctcctcagtgctgtgggggccccaggtggctctcacttgagcagtggcttg
tcagacctacccctatccacacccctttcatccccaggtttccgagagagcgctttttcc
ttctccatgctggctgctggggtcatgcatgcggtagccaccgcctgcagcctgggcaag
ctggtgagctgtggctgtggctggaagggcagtggtgagcaggatcgactgagggcgaaa
ctgctgcagctgcaggcactatcgcggggcaagagcttttcccactccctgcccagctcg
ggccccggctccggtcccagccctggcccccaggacacgtgggaatggggcggctgtaac
catgacatggacttcggggagaagttctctcgggattttttggattccagggaagctcct
cgggacatccaggcacgaatgcggatccacaacaacagggtggggcgtcaggtggtaact
gaaaacctgaagcggaaatgcaagtgccatggtacgtcaggcagctgccagctcaagacg
tgctggagggcacccccagagttccgggcagtgggagcagccttgagggagcggctggac
cgggccatcttcattgatactcacaaccgcaactccggagcctttcaaccccgtcttcgg
ccccgtcgcctttcaggagagctggtctacttcgagaactctcctgacttctgtgagcga
gaccccactgtgggctccccaggcacgcagggccgggcctgcaacaagacgagccaccag
ctgggtagctgtggcagcctgtgctgtggccgagggcacaacgtgctccggcagacccga
gtcgagcgctgtaattgccgcttccactggtgctgctacgtgctgtgtgacgagtgcaag
gtcacagagtgggtcaatgtgtgtaagtga

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