KEGG   Ailuropoda melanoleuca (giant panda): 100473854
Entry
100473854         CDS       T01329                                 
Symbol
WNT5B
Name
(RefSeq) protein Wnt-5b isoform X3
  KO
K00444  wingless-type MMTV integration site family, member 5
Organism
aml  Ailuropoda melanoleuca (giant panda)
Pathway
aml04150  mTOR signaling pathway
aml04310  Wnt signaling pathway
aml04360  Axon guidance
aml04390  Hippo signaling pathway
aml04550  Signaling pathways regulating pluripotency of stem cells
aml04916  Melanogenesis
aml04934  Cushing syndrome
aml05010  Alzheimer disease
aml05022  Pathways of neurodegeneration - multiple diseases
aml05165  Human papillomavirus infection
aml05200  Pathways in cancer
aml05205  Proteoglycans in cancer
aml05217  Basal cell carcinoma
aml05224  Breast cancer
aml05225  Hepatocellular carcinoma
aml05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:aml00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100473854 (WNT5B)
   04390 Hippo signaling pathway
    100473854 (WNT5B)
   04150 mTOR signaling pathway
    100473854 (WNT5B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100473854 (WNT5B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100473854 (WNT5B)
  09158 Development and regeneration
   04360 Axon guidance
    100473854 (WNT5B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100473854 (WNT5B)
   05205 Proteoglycans in cancer
    100473854 (WNT5B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100473854 (WNT5B)
   05226 Gastric cancer
    100473854 (WNT5B)
   05217 Basal cell carcinoma
    100473854 (WNT5B)
   05224 Breast cancer
    100473854 (WNT5B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100473854 (WNT5B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100473854 (WNT5B)
   05022 Pathways of neurodegeneration - multiple diseases
    100473854 (WNT5B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100473854 (WNT5B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:aml00536]
    100473854 (WNT5B)
Glycosaminoglycan binding proteins [BR:aml00536]
 Heparan sulfate / Heparin
  Morphogens
   100473854 (WNT5B)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100473854
NCBI-ProteinID: XP_019649301
Ensembl: ENSAMEG00000004263
LinkDB
Position
16:complement(2091395..2119502)
AA seq 329 aa
MNPVQRPEMFIIGAQPVCSQLPGLSPGQRKLCQLYQEHMAYIGEGAKTGIKECQYQFRQR
RWNCSTVDNASVFGRVMQIGSRETAFTYAVSAAGVVNAISRACREGELSTCGCSRSARPK
DLPRDWLWGGCGDNVEYGYRFAKEFVDAREREKNFAKGSEEQGRVLMNLQNNEAGRRAVY
RMADVACKCHGVSGSCSLKTCWLQLAEFRKVGDQLKEKYDSAAAMRITRRGKLELVNSRF
NQPTPEDLVYVDPSPDYCLRNETTGSLGTQGRLCNKTSEGMDGCELMCCGRGYDQFKSVQ
VERCHCKFHWCCYVKCKKCTEIVDQYVCK
NT seq 990 nt   +upstreamnt  +downstreamnt
atgaacccggtgcagagacccgagatgtttatcatcggtgcccagcccgtgtgcagccag
cttcctgggctctcccctggccagaggaagctgtgccaactgtaccaggagcacatggcc
tatattggggagggagccaagacgggcatcaaggagtgccagtaccagttccggcagcgg
cggtggaactgtagcacggtggacaacgcgtctgtcttcgggagagtcatgcagataggg
agccgggagaccgccttcacctacgcggtgagcgccgccggggtggtgaacgccatcagc
cgggcttgcagggagggggagctctccacgtgcggctgcagccggtcggcgcggcccaag
gaccttccccgggactggctgtggggcggctgcggggacaacgtggagtacggctaccgc
tttgctaaggagttcgtggatgcccgcgagcgggagaagaactttgccaaggggtcggag
gagcaaggccgagtgctcatgaacctgcagaacaacgaggcggggcggagggcggtgtac
aggatggccgacgtggcctgcaaatgccacggcgtctcggggtcctgcagcctcaagacg
tgctggctgcagctggctgagttccgcaaggtgggggaccagctgaaggagaagtacgac
agcgcggccgccatgcgcatcacccgcaggggcaagctggagctggtcaacagccgcttc
aaccagcccaccccggaggacctggtctacgtggaccccagcccagactactgcctgcgc
aacgagaccaccggctcgctgggcacgcagggccgcctgtgcaacaagacgtcggagggc
atggacggctgcgagctcatgtgctgcggccgcggctacgaccagttcaagagcgtgcag
gtggagcgctgccactgcaaattccactggtgctgctacgtcaagtgcaagaagtgcacg
gagatcgtcgaccagtacgtctgtaaatag

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