KEGG   Nomascus leucogenys (northern white-cheeked gibbon): 100607954
Entry
100607954         CDS       T03265                                 
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b isoform X2
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
nle  Nomascus leucogenys (northern white-cheeked gibbon)
Pathway
nle04150  mTOR signaling pathway
nle04310  Wnt signaling pathway
nle04390  Hippo signaling pathway
nle04550  Signaling pathways regulating pluripotency of stem cells
nle04916  Melanogenesis
nle04934  Cushing syndrome
nle05010  Alzheimer disease
nle05022  Pathways of neurodegeneration - multiple diseases
nle05165  Human papillomavirus infection
nle05200  Pathways in cancer
nle05205  Proteoglycans in cancer
nle05217  Basal cell carcinoma
nle05224  Breast cancer
nle05225  Hepatocellular carcinoma
nle05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:nle00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100607954 (WNT2B)
   04390 Hippo signaling pathway
    100607954 (WNT2B)
   04150 mTOR signaling pathway
    100607954 (WNT2B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100607954 (WNT2B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100607954 (WNT2B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100607954 (WNT2B)
   05205 Proteoglycans in cancer
    100607954 (WNT2B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100607954 (WNT2B)
   05226 Gastric cancer
    100607954 (WNT2B)
   05217 Basal cell carcinoma
    100607954 (WNT2B)
   05224 Breast cancer
    100607954 (WNT2B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100607954 (WNT2B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100607954 (WNT2B)
   05022 Pathways of neurodegeneration - multiple diseases
    100607954 (WNT2B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100607954 (WNT2B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:nle00536]
    100607954 (WNT2B)
Glycosaminoglycan binding proteins [BR:nle00536]
 Heparan sulfate / Heparin
  Morphogens
   100607954 (WNT2B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 100607954
NCBI-ProteinID: XP_003268034
Ensembl: ENSNLEG00000004104
LinkDB
Position
12:complement(63485718..63548141)
AA seq 299 aa
MRSVGEGAREWIRECQHQFRHHRWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVH
AITRACSQGELSVCSCDPYTRGRHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKD
ARALMNLHNNRCGRTAVRRFLKLECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGA
VQVMATQDGANFTAARQGYRRATRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGT
DGCEIMCCGRGYDTTRVTRVTQCECKFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq 900 nt   +upstreamnt  +downstreamnt
atgcgttcagtgggcgagggtgcccgagaatggatccgagagtgtcagcaccaattccgc
caccaccgctggaactgtaccaccctggaccgggaccacaccgtctttggccgtgtcatg
ctcagaagtagccgagaggcagcttttgtatatgccatctcatcagcaggggtagtccac
gctattactcgtgcctgtagccaaggtgaactgagtgtgtgcagctgtgacccctatacc
cgtggccgacaccatgaccagcgtggggactttgactggggtggctgcagtgacaacatc
cactatggtgtccgttttgccaaggccttcgtggatgccaaggagaagaggcttaaggat
gcccgggccctcatgaacttacataataaccgctgtggtcgcacggctgtgcggcggttt
ctgaagctggagtgtaagtgccatggcgtgagtggttcctgtactctgcgcacctgctgg
cgtgcactctcagatttccgccgcacaggtgattacctgcggcggcgctatgatggggct
gtgcaggtgatggccacccaggatggtgccaacttcaccgcagcccgccaaggctatcgc
cgtgccacccggactgatcttgtctactttgacaactctccagattactgtgtcttggac
aaggctgcaggttccctaggcactgcaggccgtgtctgcagcaagacttcaaaaggaaca
gacggttgtgaaatcatgtgctgtggccgagggtacgacacaactcgagtcacccgtgtt
acccagtgtgagtgcaaattccactggtgctgtgctgtacggtgcaaggaatgcagaaat
actgtggacgtccatacttgcaaggcccccaagaaggcagagtggctggaccagacctga

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