KEGG   Myotis davidii (David's myotis): 102771010
Entry
102771010         CDS       T02992                                 
Symbol
WNT5A
Name
(RefSeq) Wnt family member 5A
  KO
K00444  wingless-type MMTV integration site family, member 5
Organism
myd  Myotis davidii (David's myotis)
Pathway
myd04150  mTOR signaling pathway
myd04310  Wnt signaling pathway
myd04360  Axon guidance
myd04390  Hippo signaling pathway
myd04550  Signaling pathways regulating pluripotency of stem cells
myd04916  Melanogenesis
myd04934  Cushing syndrome
myd05010  Alzheimer disease
myd05022  Pathways of neurodegeneration - multiple diseases
myd05165  Human papillomavirus infection
myd05200  Pathways in cancer
myd05205  Proteoglycans in cancer
myd05217  Basal cell carcinoma
myd05224  Breast cancer
myd05225  Hepatocellular carcinoma
myd05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:myd00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102771010 (WNT5A)
   04390 Hippo signaling pathway
    102771010 (WNT5A)
   04150 mTOR signaling pathway
    102771010 (WNT5A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102771010 (WNT5A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102771010 (WNT5A)
  09158 Development and regeneration
   04360 Axon guidance
    102771010 (WNT5A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102771010 (WNT5A)
   05205 Proteoglycans in cancer
    102771010 (WNT5A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102771010 (WNT5A)
   05226 Gastric cancer
    102771010 (WNT5A)
   05217 Basal cell carcinoma
    102771010 (WNT5A)
   05224 Breast cancer
    102771010 (WNT5A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102771010 (WNT5A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102771010 (WNT5A)
   05022 Pathways of neurodegeneration - multiple diseases
    102771010 (WNT5A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102771010 (WNT5A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:myd00536]
    102771010 (WNT5A)
Glycosaminoglycan binding proteins [BR:myd00536]
 Heparan sulfate / Heparin
  Morphogens
   102771010 (WNT5A)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 102771010
NCBI-ProteinID: XP_015426492
LinkDB
Position
Un
AA seq 348 aa
MKKSTGILSPGVALGTAGSAMSSKFFLMALAIFFSFAQVVIEANSWWSLGMNNPVQMSEV
YIIGAQPLCSQLAGLSQGQKKLCHLYQDHMQYIGEGAKTGIKECQYQFRHRRWNCSTVDN
TSVFGRVMQIGRRPLNIFYIYINFSPRKSPYDNIDYGYRFAKEFVDARERERIHAKGSYE
SARILMNLHNNEAGRRTVYNLADVACKCHGVSGSCSLKTCWLQLADFRKVGDALKEKYDS
AAAMRLNGRGKLVQVNSRFNSPTTQDLVYIDPSPDYCVRNESTGSLGTQGRLCNKTSEGM
DGCELMCCGRGYDQFKTVQTERCHCKFHWCCYVKCKKCTEIVDQFVCK
NT seq 1047 nt   +upstreamnt  +downstreamnt
atgaagaagtccactggaatattaagcccaggagttgctttggggacggctgggagtgcc
atgtcttccaagttcttcctaatggctttggccatatttttctccttcgcccaggttgta
atagaagccaattcttggtggtcgctaggtatgaataaccctgttcagatgtcagaagta
tatatcataggagcacagcctctctgcagccagctggcaggactctctcaaggacagaag
aaactctgccacttgtaccaggaccacatgcagtacattggtgaaggcgcgaagacgggc
atcaaagaatgccagtatcagttccggcatcggcgatggaactgcagcactgtggataac
acctccgtgtttggcagggttatgcagataggtaggagaccacttaacatattttatata
tatataaacttttctcctagaaaaagtccttacgacaacattgactacggctaccgcttc
gccaaggagttcgtggacgcgcgcgagcgggagcgcatccacgccaaaggctcctacgag
agcgcgcgcatcctcatgaacctgcacaacaacgaggccggccgcaggacagtgtacaac
ctggccgatgtggcctgcaagtgccacggggtgtccggctcctgtagcctcaagacgtgc
tggctgcagctggccgacttccgcaaggtgggcgacgccctgaaggagaagtatgacagc
gcggcggccatgcggctcaacggccggggcaagctggtgcaggtgaacagccgcttcaac
tcgcccaccacgcaggacctggtctacatcgaccccagccccgattactgcgtgcgcaac
gagagcacgggctcgctgggcacgcagggccgcctgtgcaacaagacgtccgagggcatg
gacggctgcgagctcatgtgctgcggccgcggctacgaccagttcaagaccgtgcagacc
gagcgctgccactgcaagttccactggtgctgctacgtcaagtgcaagaagtgcacggag
atcgtggaccagttcgtgtgcaaatag

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