KEGG   Myotis yumanensis (Yuma myotis): 138996283
Entry
138996283         CDS       T10762                                 
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b isoform X1
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
myum  Myotis yumanensis (Yuma myotis)
Pathway
myum04150  mTOR signaling pathway
myum04310  Wnt signaling pathway
myum04390  Hippo signaling pathway
myum04519  Cadherin signaling
myum04550  Signaling pathways regulating pluripotency of stem cells
myum04916  Melanogenesis
myum04934  Cushing syndrome
myum05010  Alzheimer disease
myum05022  Pathways of neurodegeneration - multiple diseases
myum05165  Human papillomavirus infection
myum05200  Pathways in cancer
myum05205  Proteoglycans in cancer
myum05217  Basal cell carcinoma
myum05224  Breast cancer
myum05225  Hepatocellular carcinoma
myum05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:myum00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    138996283 (WNT2B)
   04390 Hippo signaling pathway
    138996283 (WNT2B)
   04150 mTOR signaling pathway
    138996283 (WNT2B)
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    138996283 (WNT2B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    138996283 (WNT2B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    138996283 (WNT2B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    138996283 (WNT2B)
   05205 Proteoglycans in cancer
    138996283 (WNT2B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    138996283 (WNT2B)
   05226 Gastric cancer
    138996283 (WNT2B)
   05217 Basal cell carcinoma
    138996283 (WNT2B)
   05224 Breast cancer
    138996283 (WNT2B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    138996283 (WNT2B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    138996283 (WNT2B)
   05022 Pathways of neurodegeneration - multiple diseases
    138996283 (WNT2B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    138996283 (WNT2B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:myum00536]
    138996283 (WNT2B)
Glycosaminoglycan binding proteins [BR:myum00536]
 Heparan sulfate / Heparin
  Morphogens
   138996283 (WNT2B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 138996283
NCBI-ProteinID: XP_070253472
LinkDB
Position
Unknown
AA seq 393 aa
MLKLGGAENAAQLPPRRARAPVPAPAPRPAAPDGSRAAARLSLACLLLLLLLTLPARVDT
SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC
TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD
QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK
CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD
LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK
FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq 1182 nt   +upstreamnt  +downstreamnt
atgctgaagctgggtggtgcggagaacgccgcgcagctcccccctcggcgtgcccgcgct
cctgtccccgcgcccgcgcccagacctgcggcccccgacggctcccgggctgcggcccgc
ctaagccttgcctgcttgctgctgctgctgctgctgacgctgccggcccgcgtagatacg
tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaatatccctggtctg
gtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctcggtgggcgag
ggtgcccgagaatggatccgagagtgtcagcaccagttccgccaccaccgctggaactgc
accaccctggaccgggaccacactgtctttggccgtgtcatgctcagaagcagccgggag
gcagcgtttgtatatgccatctcgtcagcaggggtagttcatgctatcacccgcgcctgt
agccagggggaactgagtgtgtgcagctgtgacccctatacccgtggccgacaccatgat
caacgtggggactttgactggggtggctgcagtgacaacatacactacggcgttcgcttt
gccaaggccttcgtggatgccaaggagaagaggctcaaggatgcccgggccctcatgaac
ttacataacaaccgctgtggtcgcacggctgtacggcggtttctgaagctggagtgtaag
tgccatggcgtgagtggctcctgtactctgcgcacctgctggcgtgcgctctcagacttc
cgccgcacaggtgattacctgcggcggcgctatgatggggctgtgcaggtgacagcaacc
caggatggcgccaacttcacagcagcccgccaaggctatcgccgtgccactcggactgac
cttgtctactttgacaactccccagactactgtgtcttggacaaggctgcaggttcccta
ggcactgcaggccgtgtctgcagcaagacatctaaagggacagatggctgtgaaatcatg
tgctgtggccgagggtatgacacaactcgagtcacccgtgtcacccagtgtgagtgcaaa
ttccactggtgctgcgccgtgcggtgcaaggagtgcagaaacactgtggacgtccacacc
tgcaaggcccccaagaaggcagagtggctggaccagacctga

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