Trachypithecus francoisi (Francois's langur): 117094507
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Entry
117094507 CDS
T07225
Symbol
WNT10A
Name
(RefSeq) protein Wnt-10a
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
tfn05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
tfn00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
117094507 (WNT10A)
04390 Hippo signaling pathway
117094507 (WNT10A)
04150 mTOR signaling pathway
117094507 (WNT10A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
117094507 (WNT10A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
117094507 (WNT10A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
117094507 (WNT10A)
05205 Proteoglycans in cancer
117094507 (WNT10A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
117094507 (WNT10A)
05226 Gastric cancer
117094507 (WNT10A)
05217 Basal cell carcinoma
117094507 (WNT10A)
05224 Breast cancer
117094507 (WNT10A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
117094507 (WNT10A)
09164 Neurodegenerative disease
05010 Alzheimer disease
117094507 (WNT10A)
05022 Pathways of neurodegeneration - multiple diseases
117094507 (WNT10A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
117094507 (WNT10A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
tfn00536
]
117094507 (WNT10A)
Glycosaminoglycan binding proteins [BR:
tfn00536
]
Heparan sulfate / Heparin
Morphogens
117094507 (WNT10A)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
DUF7539
Ebola_NP
Motif
Other DBs
NCBI-GeneID:
117094507
NCBI-ProteinID:
XP_033086092
LinkDB
All DBs
Position
Unknown
AA seq
417 aa
AA seq
DB search
MGSAHPRPWLRLRPQPQPRPALWVLLFFLLLLAAAMPRSAPNDILDLRLPPEPVLNANTV
CLTLPGLSRRQMEVCVRHPDVAASAIQGIQIAIHECQHQFRDQRWNCSSLETRNKIPYES
PIFSRGFRESAFAYAIAAAGVVHAVSNACALGKLKACGCDASRRGDEEAFRRKLHRLQLD
ALQRGKGLSHGVPEHPALPTASPGLQDSWEWGGCSPDMGFGERFSKDFLDSREPHRDIHA
RMRLHNNRVGRQAVMENMRRKCKCHGTSGSCQLKTCWQVTPEFRTVGALLRSRFHRATLI
RPHNRNGGQLEPGPAGAPSPAPGAPGPRRRASPADLVYFEKSPDFCEREPRLDSAGTVGR
LCNKSSAGSDGCGSMCCGRGHNILRQTRSERCHCRFHWCCFVVCEECRITEWVSVCK
NT seq
1254 nt
NT seq
+upstream
nt +downstream
nt
atgggcagcgcccaccctcgcccctggctgcggctccgaccccagccccagccgcggcca
gcgctctgggtgctcctgttcttcctactgctgctggctgctgccatgcccaggtcagca
cccaatgacattctggacctccgcctccccccggagcctgtgctcaatgccaacacagtg
tgcctaacattgccaggcctgagccggcggcagatggaggtgtgtgtgcgtcaccctgat
gtggctgcctcagccatacagggcatccagatcgctatccacgaatgccaacaccaattc
agggaccagcgctggaactgctcaagcctggagactcgcaacaagatcccctatgaaagt
cccatcttcagcagaggtttccgagagagcgcttttgcctacgccatcgcggcagctggt
gttgtacacgccgtgtccaatgcatgtgccctgggcaaactaaaggcctgtggctgcgac
gcgtcccggcgaggggacgaggaggccttccgtaggaagctgcaccgcctacaactggac
gcactgcagcgtggtaagggcctgagccatggggtcccggaacacccagccctgcccaca
gccagcccaggcctgcaggactcctgggagtggggcggctgcagccccgacatgggcttc
ggggagcgcttctctaaggactttctggactcccgggaacctcacagagacatccacgca
agaatgaggcttcacaacaaccgagttgggaggcaggcagtgatggagaacatgcggcgg
aagtgcaagtgccacggcacgtcaggcagctgccagctcaagacgtgctggcaggtgacg
cccgagttccgcaccgtgggggcgctgctgcgcagccgcttccaccgcgccacgctcatc
cggccgcacaaccgcaacggcggccagctggagccgggcccagcgggggcaccctcgccg
gctcccggagctcccgggcctcgccgccgggccagccccgccgacctggtctacttcgaa
aagtcgcccgacttctgcgagcgcgagccgcgcctggactcggcgggcaccgtgggccgc
ctgtgcaacaagagcagcgcgggctcggatggctgcggcagcatgtgttgcggccgcggc
cacaacatcctgcgccagacgcgcagcgagcgctgccactgccgcttccactggtgctgc
ttcgtggtctgcgaagagtgccgcatcaccgagtgggtcagcgtctgcaagtga
DBGET
integrated database retrieval system