Trachypithecus francoisi (Francois's langur): 117076502
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Entry
117076502 CDS
T07225
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
tfn
Trachypithecus francoisi (Francois's langur)
Pathway
tfn04150
mTOR signaling pathway
tfn04310
Wnt signaling pathway
tfn04390
Hippo signaling pathway
tfn04550
Signaling pathways regulating pluripotency of stem cells
tfn04916
Melanogenesis
tfn04934
Cushing syndrome
tfn05010
Alzheimer disease
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Pathways of neurodegeneration - multiple diseases
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Human papillomavirus infection
tfn05200
Pathways in cancer
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Proteoglycans in cancer
tfn05217
Basal cell carcinoma
tfn05224
Breast cancer
tfn05225
Hepatocellular carcinoma
tfn05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
tfn00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
117076502 (WNT2B)
04390 Hippo signaling pathway
117076502 (WNT2B)
04150 mTOR signaling pathway
117076502 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
117076502 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
117076502 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
117076502 (WNT2B)
05205 Proteoglycans in cancer
117076502 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
117076502 (WNT2B)
05226 Gastric cancer
117076502 (WNT2B)
05217 Basal cell carcinoma
117076502 (WNT2B)
05224 Breast cancer
117076502 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
117076502 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
117076502 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
117076502 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
117076502 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
tfn00536
]
117076502 (WNT2B)
Glycosaminoglycan binding proteins [BR:
tfn00536
]
Heparan sulfate / Heparin
Morphogens
117076502 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
117076502
NCBI-ProteinID:
XP_033055975
LinkDB
All DBs
Position
Unknown
AA seq
391 aa
AA seq
DB search
MLRPGGAEEAAQLPLRRARAPVPVPSPAVPDGSRASARLGLACLLLLLLLTLPARVDTSW
WYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNCTT
LDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHDQR
GDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECKCH
GVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVMATQDGANFTAARQGYRRATRTDLV
YFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECKFH
WCCAVRCKECRNTVDVHTCKAPKTAEWLDQT
NT seq
1176 nt
NT seq
+upstream
nt +downstream
nt
atgctgagaccgggtggtgcggaggaagctgcgcagctcccgcttcggcgcgcccgcgcc
ccggtccctgtgccctcgcctgcggtccccgacggctcccgggcttcggcccgcctaggt
cttgcctgccttctgctcctgctgctgctgacgctgccggcccgcgtagacacgtcctgg
tggtacattggggcactgggggcacgagtgatctgtgacaatatccctggtttggtgagc
cggcagcggcagctgtgccagcgttacccagacatcatgcgttcagtgggcgagggtgcc
cgagaatggatccgagagtgtcagcaccaattccgccaccaccgctggaactgtaccacc
ctggaccgggaccacactgtctttggccgtgtcatgctcagaagtagccgagaagcagct
tttgtatatgccatctcatcagcaggggtagtccatgctattactcgtgcctgtagccag
ggtgaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgaccagcgt
ggggactttgactggggtggctgcagtgacaacatccattatggtgtccgttttgccaag
gccttcgtggatgccaaggagaagaggcttaaggatgcccgggccctcatgaacttacat
aataaccgttgtggtcgcacggctgtgcggcggtttctgaagctggagtgtaagtgccat
ggcgtgagtggttcctgtactctgcgcacctgctggcgtgcgctctcagatttccgccgc
acaggtgattacctgcggcggcgctatgatggggctgtgcaggtgatggccacgcaggat
ggtgccaacttcaccgcagcccgccaaggctatcgccgtgccacccggactgatcttgtc
tactttgacaactccccagattactgtgtcttggacaaggctgcaggttccctaggcact
gcaggccgtgtctgcagcaagacatcaaaaggaacagacggttgtgaaatcatgtgctgt
ggccgagggtatgacacaactcgagtcacccgtgttacccagtgtgagtgcaaattccac
tggtgctgtgctgtacggtgcaaggaatgcagaaatactgtggatgtccatacttgcaag
gcccccaagacggcagagtggctggaccagacctga
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