KEGG   Myotis brandtii (Brandt's bat): 102240132
Entry
102240132         CDS       T02920                                 
Symbol
WNT5A
Name
(RefSeq) Wnt family member 5A
  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
    102240132 (WNT5A)
   04390 Hippo signaling pathway
    102240132 (WNT5A)
   04150 mTOR signaling pathway
    102240132 (WNT5A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102240132 (WNT5A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102240132 (WNT5A)
  09158 Development and regeneration
   04360 Axon guidance
    102240132 (WNT5A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102240132 (WNT5A)
   05205 Proteoglycans in cancer
    102240132 (WNT5A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102240132 (WNT5A)
   05226 Gastric cancer
    102240132 (WNT5A)
   05217 Basal cell carcinoma
    102240132 (WNT5A)
   05224 Breast cancer
    102240132 (WNT5A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102240132 (WNT5A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102240132 (WNT5A)
   05022 Pathways of neurodegeneration - multiple diseases
    102240132 (WNT5A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102240132 (WNT5A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:myb00536]
    102240132 (WNT5A)
Glycosaminoglycan binding proteins [BR:myb00536]
 Heparan sulfate / Heparin
  Morphogens
   102240132 (WNT5A)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 102240132
NCBI-ProteinID: XP_014396799
LinkDB
Position
Un
AA seq 347 aa
MNSGSTCRSAQKSTGILSPGVALGTAGSAMSSKFFLMALAIFFSFAQVVIEANSWWSLGM
NNPVQMSEVYIIGAQPLCSQLAGLSQGQKKLCHLYQDHMQYIGEGAKTGIKECQYQFRHR
RWNCSTVDNTSVFGRVMQIGRRDWLWGGCGDNIDYGYRFAKEFVDARERERIHAKGSYES
ARILMNLHNNEAGRRTVYNLADVACKCHGVSGSCSLKTCWLQLADFRKVGDALKEKYDSA
AAMRLNGRGKLVQVNSRFNSPTTQDLVYIDPSPDYCVRNESTGSLGTQGRLCNKTSEGMD
GCELMCCGRGYDQFKTVQTERCHCKFHWCCYVKCKKCTEIVDQFVCK
NT seq 1044 nt   +upstreamnt  +downstreamnt
atgaattccggctccacttgtcgctcggcccagaagtccactggaatattaagcccagga
gttgctttggggacggctggaagtgccatgtcttccaagttcttcctaatggctttggcc
atatttttctccttcgcccaggttgtaatagaagccaattcttggtggtcgctaggtatg
aataaccctgttcagatgtcagaagtatatatcataggagcacagcctctctgcagccag
ctggcaggactctctcaaggacagaagaaactctgccacttgtaccaggaccacatgcag
tacattggtgaaggcgcgaagacgggcatcaaagaatgccagtatcagttccggcatcgg
cgatggaactgcagcactgtggataacacctccgtgtttggcagggttatgcagataggt
aggagggactggctgtggggcggctgcggcgacaacatcgactacggctaccgcttcgcc
aaggagttcgtggacgcgcgcgagcgggagcgcatccacgccaaaggctcctacgagagc
gcgcgcatcctcatgaacctgcacaacaacgaggccggccgcaggacagtgtacaacctg
gccgatgtggcctgcaagtgccacggggtgtccggctcctgtagcctcaagacgtgctgg
ctgcagctggccgacttccgcaaggtgggcgacgccctgaaggagaagtatgacagcgcg
gcggccatgcggctcaacggccggggcaagctggtgcaggtgaacagccgcttcaactcg
cccaccacgcaggacctggtctacatcgaccccagccccgactactgcgtgcgcaatgag
agcacgggctcgctgggcacgcagggccgcctgtgcaacaagacgtccgagggcatggac
ggctgcgagctcatgtgctgcggccgcggctatgaccagttcaagaccgtgcagaccgag
cgctgccactgcaagttccactggtgctgctacgtcaagtgcaagaagtgcacggagatc
gtggaccagttcgtgtgcaaatag

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