Pan paniscus (bonobo): 100983371
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Entry
100983371 CDS
T02283
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
pps
Pan paniscus (bonobo)
Pathway
pps04150
mTOR signaling pathway
pps04310
Wnt signaling pathway
pps04390
Hippo signaling pathway
pps04550
Signaling pathways regulating pluripotency of stem cells
pps04916
Melanogenesis
pps04934
Cushing syndrome
pps05010
Alzheimer disease
pps05022
Pathways of neurodegeneration - multiple diseases
pps05165
Human papillomavirus infection
pps05200
Pathways in cancer
pps05205
Proteoglycans in cancer
pps05217
Basal cell carcinoma
pps05224
Breast cancer
pps05225
Hepatocellular carcinoma
pps05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pps00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100983371 (WNT2B)
04390 Hippo signaling pathway
100983371 (WNT2B)
04150 mTOR signaling pathway
100983371 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100983371 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100983371 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100983371 (WNT2B)
05205 Proteoglycans in cancer
100983371 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100983371 (WNT2B)
05226 Gastric cancer
100983371 (WNT2B)
05217 Basal cell carcinoma
100983371 (WNT2B)
05224 Breast cancer
100983371 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100983371 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
100983371 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
100983371 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100983371 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pps00536
]
100983371 (WNT2B)
Glycosaminoglycan binding proteins [BR:
pps00536
]
Heparan sulfate / Heparin
Morphogens
100983371 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100983371
NCBI-ProteinID:
XP_003810739
Ensembl:
ENSPPAG00000026756
UniProt:
A0A2R8ZR94
LinkDB
All DBs
Position
1:complement(114513844..114526373)
Genome browser
AA seq
391 aa
AA seq
DB search
MLRPGGAEEAAQLPLRRASAPVPVPSPAAPDGSRASARLGLACLLLLLLLTLPARVDTSW
WYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNCTT
LDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHDQR
GDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECKCH
GVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVMATQDGANFTAARQGYRRATRTDLV
YFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECKFH
WCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
1176 nt
NT seq
+upstream
nt +downstream
nt
atgctgagaccgggtggtgcggaggaagctgcgcagctcccgcttcggcgcgccagcgcc
ccggtccctgtgccgtcgcccgcggcccccgacggctcccgggcttcggcccgcctaggt
cttgcctgccttctgctcctgctgctgctgacactgccggcccgcgtagacacgtcctgg
tggtacattggggcactgggggcacgagtgatctgtgacaatatccctggtttggtgagc
cggcagcggcagctgtgccagcgttacccagacatcatgcgttcagtgggcgagggtgcc
cgagaatggatccgagagtgtcagcaccaattccgccaccaccgctggaactgtaccacc
ctggaccgggaccacaccgtctttggccgtgtcatgctcagaagtagccgagaggcagct
tttgtatatgccatctcatcagcaggggtagtccacgctattactcgtgcctgtagccag
ggtgaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgaccagcgt
ggggactttgactggggtggctgcagtgacaacatccactacggtgtccgttttgccaag
gccttcgtggatgccaaggagaagaggcttaaggatgcccgggccctcatgaacttacat
aataaccgctgtggtcgcacggctgtgcggcggtttctgaagctggagtgtaagtgccat
ggcgtgagtggttcctgtactctgcgcacctgctggcgtgcactctcagatttccgccgc
acaggtgattacctgcggcggcgctatgatggggctgtgcaggtgatggccacccaagat
ggtgccaacttcaccgcagcccgccaaggctatcgccgtgccacccggactgatcttgtc
tactttgacaactctccagattactgtgtcttggacaaggctgcaggttccctaggcact
gcaggccgtgtctgcagcaagacatcaaaaggaacagacggttgtgaaatcatgtgctgt
ggccgagggtacgacacaactcgagtcacccgtgttacccagtgtgagtgcaaattccac
tggtgctgtgctgtacggtgcaaggaatgcagaaatactgtggacgtccatacttgcaag
gcccccaagaaggcagagtggctggaccagacctga
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