KEGG   Ailuropoda melanoleuca (giant panda): 100481665
Entry
100481665         CDS       T01329                                 
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b isoform X1
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
aml  Ailuropoda melanoleuca (giant panda)
Pathway
aml04150  mTOR signaling pathway
aml04310  Wnt signaling pathway
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
    100481665 (WNT2B)
   04390 Hippo signaling pathway
    100481665 (WNT2B)
   04150 mTOR signaling pathway
    100481665 (WNT2B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100481665 (WNT2B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100481665 (WNT2B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100481665 (WNT2B)
   05205 Proteoglycans in cancer
    100481665 (WNT2B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100481665 (WNT2B)
   05226 Gastric cancer
    100481665 (WNT2B)
   05217 Basal cell carcinoma
    100481665 (WNT2B)
   05224 Breast cancer
    100481665 (WNT2B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100481665 (WNT2B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100481665 (WNT2B)
   05022 Pathways of neurodegeneration - multiple diseases
    100481665 (WNT2B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100481665 (WNT2B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:aml00536]
    100481665 (WNT2B)
Glycosaminoglycan binding proteins [BR:aml00536]
 Heparan sulfate / Heparin
  Morphogens
   100481665 (WNT2B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 100481665
NCBI-ProteinID: XP_002918296
Ensembl: ENSAMEG00000003598
UniProt: G1LA82
LinkDB
Position
2:79130247..79148501
AA seq 393 aa
MLKPGSAEDAAQLPPRRTRAPVPALAPGPAAPDGSRASARLGLACLLLLLLLTLPARVDT
SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC
TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD
QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK
CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD
LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK
FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq 1182 nt   +upstreamnt  +downstreamnt
atgctgaagccgggtagtgcggaggacgccgcgcagctcccccctcggcgcacccgcgcc
cccgtccccgcgctcgcgccaggacccgctgcccccgacggctctcgggcttcggcccgc
ctcggtctcgcctgcctgctgctgctgctgctgctgacgctgccggcccgcgtagacaca
tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaatatccctggtctg
gtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctcagtgggcgag
ggtgcccgagaatggatccgagagtgtcagcaccagttccgccaccaccgctggaactgc
accacgctggaccgggaccacactgtctttgggcgcgtcatgctcagaagcagccgggag
gcagcatttgtatatgccatctcgtcggcaggggtggtccatgctatcacccgtgcctgc
agccagggtgaactgagtgtgtgcagctgtgacccctacactcgtggccgacaccatgac
caacgtggggattttgactggggtggctgcagtgacaacatccactatggtgttcgcttt
gccaaggcctttgtggatgccaaggaaaagaggcttaaggatgcccgggccctcatgaat
ttacataacaaccgctgtggtcgcacggctgtgaggcggtttctgaaactcgagtgcaag
tgccacggcgtaagtggctcctgtaccctgcgcacctgctggcgtgcactctcagacttc
cgccgcacgggtgactatctgcggcggcgctatgatggcgccgtgcaggtgacagcaacc
caggatggcgccaacttcacggcagcccgccaaggctatcgccgtgccacccggactgac
cttgtctactttgacaactccccagactactgtgtcttggacaaggctgcaggttcccta
ggcactgcgggccgtgtctgcagcaagacatctaaagggacggatggttgcgaaatcatg
tgctgtggccgagggtatgacacaactcgagtcacccgcgtcacccagtgtgagtgcaaa
ttccactggtgctgtgcggtgcggtgcaaggagtgcagaaacactgtcgacgtccatact
tgcaaggcccccaagaaggcagagtggctggaccagacctga

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