Bos taurus (cow): 539337
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Entry
539337 CDS
T01008
Symbol
WNT10B
Name
(RefSeq) protein Wnt-10b
KO
K01357
wingless-type MMTV integration site family, member 10
Organism
bta
Bos taurus (cow)
Pathway
bta04150
mTOR signaling pathway
bta04310
Wnt signaling pathway
bta04390
Hippo signaling pathway
bta04550
Signaling pathways regulating pluripotency of stem cells
bta04916
Melanogenesis
bta04934
Cushing syndrome
bta05010
Alzheimer disease
bta05022
Pathways of neurodegeneration - multiple diseases
bta05165
Human papillomavirus infection
bta05200
Pathways in cancer
bta05205
Proteoglycans in cancer
bta05217
Basal cell carcinoma
bta05224
Breast cancer
bta05225
Hepatocellular carcinoma
bta05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
bta00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
539337 (WNT10B)
04390 Hippo signaling pathway
539337 (WNT10B)
04150 mTOR signaling pathway
539337 (WNT10B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
539337 (WNT10B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
539337 (WNT10B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
539337 (WNT10B)
05205 Proteoglycans in cancer
539337 (WNT10B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
539337 (WNT10B)
05226 Gastric cancer
539337 (WNT10B)
05217 Basal cell carcinoma
539337 (WNT10B)
05224 Breast cancer
539337 (WNT10B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
539337 (WNT10B)
09164 Neurodegenerative disease
05010 Alzheimer disease
539337 (WNT10B)
05022 Pathways of neurodegeneration - multiple diseases
539337 (WNT10B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
539337 (WNT10B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
bta00536
]
539337 (WNT10B)
Glycosaminoglycan binding proteins [BR:
bta00536
]
Heparan sulfate / Heparin
Morphogens
539337 (WNT10B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
539337
NCBI-ProteinID:
XP_010803331
BGD-bta:
BT29913
Ensembl:
ENSBTAG00000015347
VGNC:
56232
UniProt:
F1MK64
LinkDB
All DBs
Position
5:30841143..30847502
Genome browser
AA seq
391 aa
AA seq
DB search
MREEPRPRPPPSGLAGLLFLALCSRALGNEIQGLKLPGGGEPPLTANTVCLTLSGLSKQQ
LGLCLRSPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESA
FSFSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFSHSLP
SSGPGSGPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQV
VTENLKRKCKCHGTSGSCQLKTCWRAPPEFRAVGAALRERLDRAIFIDTHNRNSGAFQPR
LRPRRLSGELVYFENSPDFCERDPTVGSPGTQGRACNKTSHQLGSCGSLCCGRGHNVLRQ
TRVERCNCRFHWCCYVLCDECKVTEWVNVCK
NT seq
1176 nt
NT seq
+upstream
nt +downstream
nt
atgcgggaggagccccggccgcggcctccgccctcgggcctcgccggtctcctgttcctg
gcgttgtgcagtcgggccctcggaaatgagattcagggcttgaagctgccgggcggcggc
gagccgccgctgaccgccaacaccgtgtgcttgacgctgtcgggcctgagcaagcagcag
ctgggcctgtgcctgcgcagccccgacgtgacggcgtcggcgctccagggcctgcacatc
gcggtccacgagtgccagcaccagctgcgggaccagcgctggaactgctcggcgctcgag
ggcggcggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgagagagcgct
ttttccttctccatgctggctgctggggtcatgcatgcggtagccaccgcctgcagcctg
ggcaagctggtgagctgtggctgtggctggaagggcagtggtgagcaggatcgactgagg
gcgaaactgctgcagctgcaggcactatcgcggggcaagagcttttcccactccctgccc
agctcgggccccggctccggtcccagccctggcccccaggacacgtgggaatggggcggc
tgtaaccatgacatggacttcggggagaagttctctcgggattttttggattccagggaa
gctcctcgggacatccaggcacgaatgcggatccacaacaacagggtggggcgtcaggtg
gtaactgaaaacctgaagcggaaatgcaagtgccatggtacgtcaggcagctgccagctc
aagacgtgctggagggcacccccagagttccgggcagtgggagcagccttgagggagcgg
ctggaccgggccatcttcattgatactcacaaccgcaactccggagcctttcaaccccgt
cttcggccccgtcgcctttcaggagagctggtctacttcgagaactctcctgacttctgt
gagcgagaccccactgtgggctccccaggcacgcagggccgggcctgcaacaagacgagc
caccagctgggtagctgtggcagcctgtgctgtggccgagggcacaacgtgctccggcag
acccgagtcgagcgctgtaattgccgcttccactggtgctgctacgtgctgtgtgacgag
tgcaaggtcacagagtgggtcaatgtgtgtaagtga
DBGET
integrated database retrieval system