KEGG   Cricetulus griseus (Chinese hamster): 100761413
Entry
100761413         CDS       T02813                                 
Symbol
Wnt2b
Name
(RefSeq) protein Wnt-2b
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
cge  Cricetulus griseus (Chinese hamster)
Pathway
cge04150  mTOR signaling pathway
cge04310  Wnt signaling pathway
cge04390  Hippo signaling pathway
cge04519  Cadherin signaling
cge04550  Signaling pathways regulating pluripotency of stem cells
cge04916  Melanogenesis
cge04934  Cushing syndrome
cge05010  Alzheimer disease
cge05022  Pathways of neurodegeneration - multiple diseases
cge05165  Human papillomavirus infection
cge05200  Pathways in cancer
cge05205  Proteoglycans in cancer
cge05217  Basal cell carcinoma
cge05224  Breast cancer
cge05225  Hepatocellular carcinoma
cge05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:cge00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100761413 (Wnt2b)
   04390 Hippo signaling pathway
    100761413 (Wnt2b)
   04150 mTOR signaling pathway
    100761413 (Wnt2b)
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    100761413 (Wnt2b)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100761413 (Wnt2b)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100761413 (Wnt2b)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100761413 (Wnt2b)
   05205 Proteoglycans in cancer
    100761413 (Wnt2b)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100761413 (Wnt2b)
   05226 Gastric cancer
    100761413 (Wnt2b)
   05217 Basal cell carcinoma
    100761413 (Wnt2b)
   05224 Breast cancer
    100761413 (Wnt2b)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100761413 (Wnt2b)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100761413 (Wnt2b)
   05022 Pathways of neurodegeneration - multiple diseases
    100761413 (Wnt2b)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100761413 (Wnt2b)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:cge00536]
    100761413 (Wnt2b)
Glycosaminoglycan binding proteins [BR:cge00536]
 Heparan sulfate / Heparin
  Morphogens
   100761413 (Wnt2b)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 100761413
NCBI-ProteinID: XP_035307767
UniProt: A0A9J7H9K0
LinkDB
Position
1
AA seq 299 aa
MRSVGEGAREWIRECQHQFRHHRWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVH
AITRACSQGELSVCSCDPYTRGRHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKD
ARALMNLHNNRCGRTAVRRFLKLECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGA
VQVTATQDGANFTAARQGYRHATRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGT
DGCEIMCCGRGYDTTRVTRVTQCECKFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq 900 nt   +upstreamnt  +downstreamnt
atgcgctcagtgggtgaaggtgcccgagaatggatccgagagtgtcagcaccagttccgc
catcaccgctggaactgcaccacactggaccgggaccatactgtctttggccgtgtcatg
cttagaagtagccgggaagcagcatttgtatatgccatctcatcagctggagtggtccat
gctatcactcgggcctgcagccagggtgaattgagcgtgtgcagctgtgacccatatacc
cgtggtcggcaccatgaccaacgaggggactttgattggggtggctgtagtgacaatatc
cactatggtgtccgctttgccaaggcttttgtggatgccaaagagaagaggcttaaggat
gcccgggccctcatgaacttacataacaaccgctgtggtcgcacggctgtgcggcgattt
ctgaagctggaatgtaagtgtcatggtgtgagtggctcctgtactctacgcacctgctgg
agagcactctcagacttccgccgcactggtgactacctgaggcggaggtatgatggggct
gtgcaggtgactgccacccaggatggtgccaacttcacagcagcccgccaaggctatcgc
catgccacccggactgatcttgtctactttgacaactcccctgactactgtgtcttggac
aaggctgcaggttccctaggtactgcaggccgggtctgcagcaagacatctaaaggaaca
gatggttgtgaaatcatgtgttgtggtcgagggtacgacacaactcgagtcacccgtgtc
acccaatgtgagtgcaaattccactggtgctgtgctgtgcggtgcaaagagtgcagaaac
actgtggatgtccatacttgcaaggcccccaagaaggcagagtggctggaccagacctga

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