KEGG   Myotis brandtii (Brandt's bat): 102241642
Entry
102241642         CDS       T02920                                 
Symbol
WNT5B
Name
(RefSeq) Wnt family member 5B
  KO
K00444  wingless-type MMTV integration site family, member 5
Organism
myb  Myotis brandtii (Brandt's bat)
Pathway
myb04150  mTOR signaling pathway
myb04310  Wnt signaling pathway
myb04360  Axon guidance
myb04390  Hippo signaling pathway
myb04550  Signaling pathways regulating pluripotency of stem cells
myb04916  Melanogenesis
myb04934  Cushing syndrome
myb05010  Alzheimer disease
myb05022  Pathways of neurodegeneration - multiple diseases
myb05165  Human papillomavirus infection
myb05200  Pathways in cancer
myb05205  Proteoglycans in cancer
myb05217  Basal cell carcinoma
myb05224  Breast cancer
myb05225  Hepatocellular carcinoma
myb05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:myb00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102241642 (WNT5B)
   04390 Hippo signaling pathway
    102241642 (WNT5B)
   04150 mTOR signaling pathway
    102241642 (WNT5B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102241642 (WNT5B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102241642 (WNT5B)
  09158 Development and regeneration
   04360 Axon guidance
    102241642 (WNT5B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102241642 (WNT5B)
   05205 Proteoglycans in cancer
    102241642 (WNT5B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102241642 (WNT5B)
   05226 Gastric cancer
    102241642 (WNT5B)
   05217 Basal cell carcinoma
    102241642 (WNT5B)
   05224 Breast cancer
    102241642 (WNT5B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102241642 (WNT5B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102241642 (WNT5B)
   05022 Pathways of neurodegeneration - multiple diseases
    102241642 (WNT5B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102241642 (WNT5B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:myb00536]
    102241642 (WNT5B)
Glycosaminoglycan binding proteins [BR:myb00536]
 Heparan sulfate / Heparin
  Morphogens
   102241642 (WNT5B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 102241642
NCBI-ProteinID: XP_005865982
LinkDB
Position
Un
AA seq 358 aa
MPGLLLLAAALLSSWAQLPAEASSWWSLAMNPVQRPEMFIIGAQPVCSQLPGLSPGQRKL
CQLYQEHMAYIGEGAKMGIKECQHQFRQRRWNCSTVDDTSVFGRVMQIGSRETAFTYAVS
AAGVVNAISRACREGELSTCGCSRTARPKDLPRDWLWGGCGDNVEYGYRFAKEFVDARER
EKNFAKGSEEQGRVLMNLQNNEAGRRAVYKMADVACKCHGVSGSCSLKTCWLQLAEFRKV
GDQLKEKYDSAAAMRITRKGKLELVNSRFNQPTPEDLVYVDPSPDYCLRNETTGSLGTQG
RLCNKTSEGMDGCELMCCGRGYDQFKSVQVERCHCKFHWCCFVKCRKCTEVVDQHVCK
NT seq 1077 nt   +upstreamnt  +downstreamnt
atgccaggcctgctgctgctcgctgctgcgctgctctccagctgggctcagctcccagcc
gaagccagctcctggtggtcgctagctatgaacccggtgcagagacctgagatgttcatc
attggtgcccagcctgtgtgcagccagcttcctgggctctccccgggccagagaaagctg
tgccagttgtaccaggagcacatggcctacataggggagggagccaagatgggcatcaag
gagtgccagcaccagttccggcagaggcggtggaactgcagcaccgtggacgacacctct
gtctttgggagggtcatgcagatagggagccgggagacggccttcacctatgctgtgagt
gccgcgggggtggtgaacgccatcagcagggcctgccgagagggtgagctgtccacatgt
ggctgcagcaggacagcgcggcccaaggaccttccccgggactggctgtggggcggctgt
ggggacaacgtggagtacggctaccggtttgctaaggagtttgtggatgcccgggagcgg
gagaagaactttgccaagggatcggaggagcagggccgggtgcttatgaacctgcagaac
aacgaggcgggtcgaagggctgtgtataagatggcagatgtagcctgcaaatgccatggc
gtctctgggtcctgcagcctcaagacctgctggctccagctggctgagttccgcaaggtg
ggggaccagctgaaggagaagtacgacagcgccgctgccatgcgcatcacccgcaaaggc
aagctggagctggtcaacagccgcttcaaccagcccaccccggaggacctggtgtatgtg
gaccccagccctgactactgcctgcgcaacgagaccacgggctccctgggcacccagggc
cgcctctgcaacaagacctcggagggcatggatggctgcgagctcatgtgctgcggccgc
ggctacgaccagtttaagagcgtccaggtggagcgctgccactgcaagttccactggtgc
tgcttcgtcaagtgcaggaagtgcacggaggtcgtcgaccagcacgtctgcaaatag

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