Ovis aries (sheep): 101102299
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Entry
101102299 CDS
T03117
Symbol
WNT10B
Name
(RefSeq) protein Wnt-10b
KO
K01357
wingless-type MMTV integration site family, member 10
Organism
oas
Ovis aries (sheep)
Pathway
oas04150
mTOR signaling pathway
oas04310
Wnt signaling pathway
oas04390
Hippo signaling pathway
oas04550
Signaling pathways regulating pluripotency of stem cells
oas04916
Melanogenesis
oas04934
Cushing syndrome
oas05010
Alzheimer disease
oas05022
Pathways of neurodegeneration - multiple diseases
oas05165
Human papillomavirus infection
oas05200
Pathways in cancer
oas05205
Proteoglycans in cancer
oas05217
Basal cell carcinoma
oas05224
Breast cancer
oas05225
Hepatocellular carcinoma
oas05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
oas00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
101102299 (WNT10B)
04390 Hippo signaling pathway
101102299 (WNT10B)
04150 mTOR signaling pathway
101102299 (WNT10B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
101102299 (WNT10B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
101102299 (WNT10B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
101102299 (WNT10B)
05205 Proteoglycans in cancer
101102299 (WNT10B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
101102299 (WNT10B)
05226 Gastric cancer
101102299 (WNT10B)
05217 Basal cell carcinoma
101102299 (WNT10B)
05224 Breast cancer
101102299 (WNT10B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
101102299 (WNT10B)
09164 Neurodegenerative disease
05010 Alzheimer disease
101102299 (WNT10B)
05022 Pathways of neurodegeneration - multiple diseases
101102299 (WNT10B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
101102299 (WNT10B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
oas00536
]
101102299 (WNT10B)
Glycosaminoglycan binding proteins [BR:
oas00536
]
Heparan sulfate / Heparin
Morphogens
101102299 (WNT10B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
101102299
NCBI-ProteinID:
XP_004023119
EnsemblRapid:
ENSOARG00020001413
UniProt:
W5NXT3
LinkDB
All DBs
Position
3:137250023..137256320
Genome browser
AA seq
391 aa
AA seq
DB search
MREQPRPRPPPSGLAGLLFLALCSRALGNEILGLKLPGGGEPPLTANTVCLTLSGLSKRQ
LGLCLRSPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESA
FSFSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPHSLP
STGPGSGPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQV
VTENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGTALRERLGRAIFIDAHNRNSGAFQPR
LRPRRLSGELVYFEKSPDFCERDPTVGSPGTRGRACNKTSRLLDGCGSLCCGRGHNVLRQ
TRVERCHCRFHWCCYVLCEECKVTEWVNVCK
NT seq
1176 nt
NT seq
+upstream
nt +downstream
nt
atgcgggagcagccccggccgcggcctccgccctcgggcctcgccggtctcctgttcctg
gcgttgtgcagtcgggccctcggcaatgagattctgggcttgaagctgccgggcggcggc
gagccgccgctgaccgccaacacagtctgcttgacgctgtcgggcctgagcaagcggcag
ctgggcctgtgcctgcgcagccccgacgtgacggcgtcggcgctccagggcctgcacatc
gcagtccacgagtgtcagcaccagctgcgcgatcagcgctggaactgctctgcgctcgag
ggcggcggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgagagagcgct
ttttccttctccatgctggctgctggggtcatgcatgcagtagccaccgcctgcagcctg
ggcaagctggtgagctgcggctgtggctggaagggcagtggtgagcaggatcgactgagg
gcgaaactgctgcagctgcaggcactatcgcggggcaaaagctttccccactccctgccc
agcacgggccctggctctggtcccagccctggtccccaggacacgtgggaatggggcggc
tgtaaccatgacatggacttcggggagaagttctctcgggattttttggattccagggaa
gctccccgggacatccaggcacgaatgcggatccacaacaacagggtggggcgtcaggtg
gtaactgaaaacttgaagcggaaatgcaagtgccatggcacgtcaggcagctgccagttc
aagacgtgctggagggcagccccagagttccgggcagtgggaacagccttgcgggagcgg
ctgggccgggccatcttcattgatgctcacaaccgcaactccggagccttccaaccccgc
cttcggccccgtcgcctctcaggagagctggtctacttcgagaagtctcctgacttctgc
gagcgagaccccactgtgggctccccaggcacgcggggccgggcctgcaacaagaccagc
cgcctgctggatggctgtggcagcctgtgctgtggccgcgggcacaacgtgctccggcag
acccgagtcgagcgctgtcattgccgcttccactggtgctgctacgtgctgtgtgaagag
tgcaaggtcacagagtgggtcaatgtgtgtaagtga
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