Trachypithecus francoisi (Francois's langur): 117090187
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Entry
117090187 CDS
T07225
Symbol
WNT10B
Name
(RefSeq) protein Wnt-10b
KO
K01357
wingless-type MMTV integration site family, member 10
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
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Melanogenesis
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Cushing syndrome
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Alzheimer disease
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Pathways of neurodegeneration - multiple diseases
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Human papillomavirus infection
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Pathways in cancer
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Proteoglycans in cancer
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Basal cell carcinoma
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Breast cancer
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Hepatocellular carcinoma
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Gastric cancer
Brite
KEGG Orthology (KO) [BR:
tfn00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
117090187 (WNT10B)
04390 Hippo signaling pathway
117090187 (WNT10B)
04150 mTOR signaling pathway
117090187 (WNT10B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
117090187 (WNT10B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
117090187 (WNT10B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
117090187 (WNT10B)
05205 Proteoglycans in cancer
117090187 (WNT10B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
117090187 (WNT10B)
05226 Gastric cancer
117090187 (WNT10B)
05217 Basal cell carcinoma
117090187 (WNT10B)
05224 Breast cancer
117090187 (WNT10B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
117090187 (WNT10B)
09164 Neurodegenerative disease
05010 Alzheimer disease
117090187 (WNT10B)
05022 Pathways of neurodegeneration - multiple diseases
117090187 (WNT10B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
117090187 (WNT10B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
tfn00536
]
117090187 (WNT10B)
Glycosaminoglycan binding proteins [BR:
tfn00536
]
Heparan sulfate / Heparin
Morphogens
117090187 (WNT10B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
117090187
NCBI-ProteinID:
XP_033078124
LinkDB
All DBs
Position
Unknown
AA seq
389 aa
AA seq
DB search
MPEEPRPRPPPSGLAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG
LCLRNPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS
FSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPHSLPSP
GPGSGSSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT
ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLR
PRRLSGELVYFEKSPDFCERDPTMGSPGTRGRACNKTSHLLDGCGSLCCGRGHNVLRQTR
VERCHCRFHWCCYVLCDECKITEWVNVCK
NT seq
1170 nt
NT seq
+upstream
nt +downstream
nt
atgccggaggagccccggccacggcctccgccctcgggcctcgcgggtctcctgttcctg
gcgttgtgcagtcgggctctaagcaatgagattctgggcctgaagttgcctggcgagccg
ccgctgacggccaacaccgtgtgcttgacgctgtccggcctgagcaagcggcagctaggc
ctgtgcctgcgcaaccccgacgtgacggcgtcggcgcttcagggtctgcacatcgcggtc
cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctcagcgctcgagggcggt
ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgagaaagtgctttttcc
ttctccatgctggctgctggggtcatgcacgcagtagccactgcctgcagcctgggcaag
ctggtgagctgtggctgtggctggaagggcagtggtgagcaggatcggctgagggccaaa
ctgctgcagctgcaggcattgtcccgaggcaagagtttcccccactctctgcccagccct
ggccctggctcaggctccagccctggcccccaggacacatgggaatggggtggctgtaac
catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc
cgggacatccaggcacgaatgcgaatccacaacaacagggtagggcgccaggtggtaact
gaaaacctgaagcggaaatgcaagtgtcatggcacgtcaggcagctgccagttcaagaca
tgctggagggcggccccagagttccgggcagtgggggccgcgttgagggagcggctgggc
cgggccatcttcatcgatacccacaaccgcaattctggagccttccagccccgtctgcgt
ccccgtcgcctctcaggagaactggtctactttgagaagtctcctgacttctgtgagcga
gaccccactatgggctccccagggacaaggggccgggcctgcaacaagaccagccacctg
ttggatggctgtggcagcctgtgctgtggccgtgggcacaacgtgctccggcagacacga
gttgagcgctgccattgccgcttccactggtgctgctatgtgctgtgtgatgagtgcaag
attacagagtgggtgaatgtgtgtaagtaa
DBGET
integrated database retrieval system
