KEGG   Camelus bactrianus (Bactrian camel): 105063697
Entry
105063697         CDS       T07534                                 
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
cbai  Camelus bactrianus (Bactrian camel)
Pathway
cbai04150  mTOR signaling pathway
cbai04310  Wnt signaling pathway
cbai04390  Hippo signaling pathway
cbai04550  Signaling pathways regulating pluripotency of stem cells
cbai04916  Melanogenesis
cbai04934  Cushing syndrome
cbai05010  Alzheimer disease
cbai05022  Pathways of neurodegeneration - multiple diseases
cbai05165  Human papillomavirus infection
cbai05200  Pathways in cancer
cbai05205  Proteoglycans in cancer
cbai05217  Basal cell carcinoma
cbai05224  Breast cancer
cbai05225  Hepatocellular carcinoma
cbai05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:cbai00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105063697 (WNT2B)
   04390 Hippo signaling pathway
    105063697 (WNT2B)
   04150 mTOR signaling pathway
    105063697 (WNT2B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105063697 (WNT2B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105063697 (WNT2B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105063697 (WNT2B)
   05205 Proteoglycans in cancer
    105063697 (WNT2B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105063697 (WNT2B)
   05226 Gastric cancer
    105063697 (WNT2B)
   05217 Basal cell carcinoma
    105063697 (WNT2B)
   05224 Breast cancer
    105063697 (WNT2B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105063697 (WNT2B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105063697 (WNT2B)
   05022 Pathways of neurodegeneration - multiple diseases
    105063697 (WNT2B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105063697 (WNT2B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:cbai00536]
    105063697 (WNT2B)
Glycosaminoglycan binding proteins [BR:cbai00536]
 Heparan sulfate / Heparin
  Morphogens
   105063697 (WNT2B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 105063697
NCBI-ProteinID: XP_010946614
UniProt: A0A9W3EFW2
LinkDB
Position
Unknown
AA seq 330 aa
MLPARVDTSWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQ
FRHHRWNCTTLDRDHTVFGRVMLRSSREAGFVYAIYCSQGELSVCSCDPYTRGRHHDQRG
DFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECKCHG
VSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTDLVY
FDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECKFHW
CCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq 993 nt   +upstreamnt  +downstreamnt
atgctgccggcccgcgtagacacgtcctggtggtacattggggcactgggggcccgagtg
atctgtgacaatatccctggtctggtgagccggcagcggcagctgtgccagcgttaccca
gacatcatgcgctcagtgggtgagggtgcccgagaatggatccgagagtgtcagcaccag
ttccgccaccaccgctggaactgcaccaccctggaccgggaccacactgtcttcggccga
gtcatgctcagaagtagccgggaggcaggctttgtatatgccatctactgtagccagggt
gaactgagtgtgtgcagctgtgacccctatacccgtggccgacaccatgaccaacgtggg
gactttgactggggtggttgcagtgacaacattcactatggtgttcgctttgccaaggcc
ttcgtggatgccaaggagaagaggcttaaggatgcccgggctctcatgaacttacataac
aaccgctgtggtcgcacggctgtgcggcggtttctgaagctggaatgtaagtgccacggc
gtgagtggctcctgtactctgcgcacctgctggcgtgctctctcagacttccgccgcaca
ggtgattacctgcggcggcgctatgacggggccgtgcaggtgacggccacccaggatggt
gctaacttcacagcagcccgccaaggctatcgccgtgccacccggactgaccttgtctac
tttgacaactccccagactactgtgttttggacaaggctgcaggttccctaggcactgca
ggccgtgtctgcagcaagacatctaaagggacagacggttgtgaaatcatgtgctgcggc
cgagggtatgacacaactcgagttacccgcgtcacccagtgtgagtgcaaattccactgg
tgctgtgctgtgcgctgcaaggaatgcagaaacactgtggacgtccatacttgcaaggcc
cccaagaaggcagagtggctggatcagacctga

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