KEGG   Carlito syrichta (Philippine tarsier): 103257117
Entry
103257117         CDS       T07836                                 
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
csyr  Carlito syrichta (Philippine tarsier)
Pathway
csyr04150  mTOR signaling pathway
csyr04310  Wnt signaling pathway
csyr04390  Hippo signaling pathway
csyr04550  Signaling pathways regulating pluripotency of stem cells
csyr04916  Melanogenesis
csyr04934  Cushing syndrome
csyr05010  Alzheimer disease
csyr05022  Pathways of neurodegeneration - multiple diseases
csyr05165  Human papillomavirus infection
csyr05200  Pathways in cancer
csyr05205  Proteoglycans in cancer
csyr05217  Basal cell carcinoma
csyr05224  Breast cancer
csyr05225  Hepatocellular carcinoma
csyr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:csyr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    103257117 (WNT2B)
   04390 Hippo signaling pathway
    103257117 (WNT2B)
   04150 mTOR signaling pathway
    103257117 (WNT2B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103257117 (WNT2B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    103257117 (WNT2B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103257117 (WNT2B)
   05205 Proteoglycans in cancer
    103257117 (WNT2B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103257117 (WNT2B)
   05226 Gastric cancer
    103257117 (WNT2B)
   05217 Basal cell carcinoma
    103257117 (WNT2B)
   05224 Breast cancer
    103257117 (WNT2B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103257117 (WNT2B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103257117 (WNT2B)
   05022 Pathways of neurodegeneration - multiple diseases
    103257117 (WNT2B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103257117 (WNT2B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:csyr00536]
    103257117 (WNT2B)
Glycosaminoglycan binding proteins [BR:csyr00536]
 Heparan sulfate / Heparin
  Morphogens
   103257117 (WNT2B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 103257117
NCBI-ProteinID: XP_008053040
Ensembl: ENSTSYG00000033599
UniProt: A0A1U7T5H3
LinkDB
Position
Unknown
AA seq 299 aa
MRSVGEGAREWIRECQHQFRHHRWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVH
AITRACSQGELSVCSCDPYTRGRHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKD
ARALMNLHNNRCGRTAVRRFLKLECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGA
VQVTATQDGANFTAARQGYRRATRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGT
DGCEIMCCGRGYDTTRVTRVTQCECKFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq 900 nt   +upstreamnt  +downstreamnt
atgcgctcggtgggcgagggcgcccgagagtggattagagagtgccagcaccagttccgc
caccaccgctggaactgcaccacgctggaccgggaccacaccgtcttcggccgcgtcatg
ctcagaagtagccgggaggcagcgttcgtgtatgccatctcatcagcaggggtggtccat
gccatcactcgtgcctgtagccagggtgaactgagtgtgtgcagctgtgacccctacacc
cgtggccgacaccatgaccaacgtggggactttgactggggtggctgcagtgacaacatc
cactatggtgtccgttttgccaaagccttcgtggatgccaaggagaagaggcttaaggat
gcccgggccctcatgaacttacataacaaccgctgtggccgcacggctgtgcggcggttt
ctgaagctggagtgcaagtgccacggcgtgagtggttcctgtactctgcgcacctgctgg
cgtgcgctctcagacttccgccgcacaggtgattacctgcggcggcgctacgatggggct
gtgcaggtgacagccacccaggatggtgccaacttcacagcagcccgccaaggctatcgc
cgtgccacccggaccgatcttgtctactttgacaactccccagactactgtgtcttggac
aaagctgcaggctccctaggcaccgcaggccgtgtctgcagcaagacatctaaaggaaca
gacggctgtgaaatcatgtgctgtggccgagggtatgacacgactcgagtcacccgtgtc
acccagtgtgagtgcaaattccactggtgctgtgctgtgcggtgcaaggagtgcagaaac
actgtggacgtccatacctgcaaggctcccaagaaggcagagtggctggaccaaacttga

DBGET integrated database retrieval system