KEGG   Macaca mulatta (rhesus monkey): 721685
Entry
721685            CDS       T01028                                 
Symbol
WNT5B
Name
(RefSeq) protein Wnt-5b
  KO
K00444  wingless-type MMTV integration site family, member 5
Organism
mcc  Macaca mulatta (rhesus monkey)
Pathway
mcc04150  mTOR signaling pathway
mcc04310  Wnt signaling pathway
mcc04360  Axon guidance
mcc04390  Hippo signaling pathway
mcc04550  Signaling pathways regulating pluripotency of stem cells
mcc04916  Melanogenesis
mcc04934  Cushing syndrome
mcc05010  Alzheimer disease
mcc05022  Pathways of neurodegeneration - multiple diseases
mcc05165  Human papillomavirus infection
mcc05200  Pathways in cancer
mcc05205  Proteoglycans in cancer
mcc05217  Basal cell carcinoma
mcc05224  Breast cancer
mcc05225  Hepatocellular carcinoma
mcc05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mcc00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    721685 (WNT5B)
   04390 Hippo signaling pathway
    721685 (WNT5B)
   04150 mTOR signaling pathway
    721685 (WNT5B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    721685 (WNT5B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    721685 (WNT5B)
  09158 Development and regeneration
   04360 Axon guidance
    721685 (WNT5B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    721685 (WNT5B)
   05205 Proteoglycans in cancer
    721685 (WNT5B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    721685 (WNT5B)
   05226 Gastric cancer
    721685 (WNT5B)
   05217 Basal cell carcinoma
    721685 (WNT5B)
   05224 Breast cancer
    721685 (WNT5B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    721685 (WNT5B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    721685 (WNT5B)
   05022 Pathways of neurodegeneration - multiple diseases
    721685 (WNT5B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    721685 (WNT5B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mcc00536]
    721685 (WNT5B)
Glycosaminoglycan binding proteins [BR:mcc00536]
 Heparan sulfate / Heparin
  Morphogens
   721685 (WNT5B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 721685
NCBI-ProteinID: XP_015006256
LinkDB
Position
11:1691948..1709174
AA seq 359 aa
MPSLLLLFTAALLSSWVQLLTDANSWWSLALNPVQRPEMFIIGAQPVCSQLPGLSPGQRK
LCQLYQEHMAYIGEGAKTGIKECQHQFRQRRWNCSTVDNVSVFGRVMQIGSRETAFTYAV
SAAGVVNAISRACREGELSTCGCSRTARPKDLPRDWLWGGCGDNVDYGYRFAKEFVDARE
REKNFAKGSEEQGRVLMNLQNNEAGRRAVYKTADVACKCHGVSGSCSLKTCWLQLAEFRK
VGDRLKEKYDSAAAMRVTRKGRLELVNSRFTQPTPEDLVYVDPSPDYCLRNESTGSLGTQ
GRLCNKTSEGMDGCELMCCGRGYNQFKSVQVERCHCKFHWCCFVKCKKCTEIVDQYICK
NT seq 1080 nt   +upstreamnt  +downstreamnt
atgcccagcctgctgctgctgttcactgctgctctgctgtccagctgggttcagcttctg
acagacgccaactcctggtggtcgttagctctgaacccggtgcagagacccgagatgttt
atcatcggtgcccagcccgtgtgcagtcagcttcctgggctctcccctggccagaggaag
ctgtgccaactgtaccaggagcacatggcctacataggggagggagccaagacaggcatc
aaggaatgccagcaccagttccggcagcggcgatggaactgcagcacggtggacaacgtg
tctgtctttgggagagtcatgcagataggtagccgtgagaccgccttcacctacgcagtg
agcgccgcaggggtggtcaacgccatcagccgggcctgccgcgagggcgaactctccacc
tgcggctgcagccggaccgcgcggcccaaggacctgccccgggactggctgtggggtggc
tgtggggacaatgtggattacggctaccgcttcgccaaggagtttgtggatgcccgggag
cgagagaagaactttgccaaaggatcggaggagcagggccgggtgctcatgaacctccag
aacaacgaggctggccgcagggctgtgtataagacagcagacgtagcctgcaaatgccac
ggcgtctcggggtcctgcagcctcaagacctgctggctacagctggccgagttccgcaag
gtgggggaccggctgaaggagaagtacgacagtgcggccgccatgcgcgtcacccgcaag
ggccggctggagctggtcaacagccgcttcacccagcccaccccggaggacctggtctac
gtggaccccagccctgactactgcctgcgcaatgagagcacgggctccctgggcacgcag
ggtcgcctctgcaacaagacctcggagggcatggatggctgtgagctcatgtgctgcggg
cgtggctacaaccagttcaagagcgtgcaggtggagcgctgccactgcaagttccactgg
tgctgcttcgtcaagtgcaagaagtgcaccgagatcgtggaccagtacatctgtaaatag

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