Canis lupus familiaris (dog): 486561
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Entry
486561 CDS
T01007
Symbol
WNT10B
Name
(RefSeq) protein Wnt-10b
KO
K01357
wingless-type MMTV integration site family, member 10
Organism
cfa
Canis lupus familiaris (dog)
Pathway
cfa04150
mTOR signaling pathway
cfa04310
Wnt signaling pathway
cfa04390
Hippo signaling pathway
cfa04550
Signaling pathways regulating pluripotency of stem cells
cfa04916
Melanogenesis
cfa04934
Cushing syndrome
cfa05010
Alzheimer disease
cfa05022
Pathways of neurodegeneration - multiple diseases
cfa05165
Human papillomavirus infection
cfa05200
Pathways in cancer
cfa05205
Proteoglycans in cancer
cfa05217
Basal cell carcinoma
cfa05224
Breast cancer
cfa05225
Hepatocellular carcinoma
cfa05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
cfa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
486561 (WNT10B)
04390 Hippo signaling pathway
486561 (WNT10B)
04150 mTOR signaling pathway
486561 (WNT10B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
486561 (WNT10B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
486561 (WNT10B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
486561 (WNT10B)
05205 Proteoglycans in cancer
486561 (WNT10B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
486561 (WNT10B)
05226 Gastric cancer
486561 (WNT10B)
05217 Basal cell carcinoma
486561 (WNT10B)
05224 Breast cancer
486561 (WNT10B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
486561 (WNT10B)
09164 Neurodegenerative disease
05010 Alzheimer disease
486561 (WNT10B)
05022 Pathways of neurodegeneration - multiple diseases
486561 (WNT10B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
486561 (WNT10B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
cfa00536
]
486561 (WNT10B)
Glycosaminoglycan binding proteins [BR:
cfa00536
]
Heparan sulfate / Heparin
Morphogens
486561 (WNT10B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
486561
NCBI-ProteinID:
XP_543687
Ensembl:
ENSCAFG00000008767
UniProt:
A0A8C0P6D0
A0A8I3PFR7
LinkDB
All DBs
Position
27:complement(40652204..40660691)
Genome browser
AA seq
389 aa
AA seq
DB search
MPEEPRPRPPPSGFAGLLLLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG
LCLRSPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS
FSMLAAGVMHAVATACSLGRLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPHSLPSP
GPGSGPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT
ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLR
PRRLSGELVYFEKSPDFCERDPTVGSPGTRGRACNKTSRLLDGCGSLCCGRGHNMLRQTR
VERCHCRFHWCCYVLCEECKVTEWVNVCK
NT seq
1170 nt
NT seq
+upstream
nt +downstream
nt
atgccggaggagccccggccgcggcctccgccctcgggcttcgcgggtctcctgctcctg
gcgctgtgcagtcgggccctcagcaatgagatcctgggcctgaagctgcccggggagccg
ccgctgaccgccaacaccgtgtgcctgacgctgtcgggcctgagcaagcggcagctgggc
ctctgcctgcgcagccccgacgtgacggcatccgcgcttcagggcctgcacatcgcggtc
cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctcggcgctcgagggcggc
ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgtgagagtgctttttcc
ttctccatgctggcggcaggggtcatgcacgcggtcgccacggcctgcagcctgggcagg
ctagtgagctgcggctgcggctggaagggcagtggtgagcaggaccggctgagggccaag
ctgctgcagctgcaggctctgtcccggggcaagagtttcccccactccctgcccagccct
ggccccggctcaggtcccagccctggcccccaggacacatgggaatggggtggctgtaac
catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc
cgggacatccaggcaagaatgcgaatccacaacaacagggtggggcgacaggtggtaact
gaaaacctgaagcggaaatgcaagtgccacggcacgtcgggcagctgccagttcaagacg
tgctggagggcggccccagagttccgggcagtgggggcagccctgagggagcggctgggt
cgggccatcttcatcgatacccacaaccgcaactccggagccttccagccccgcctgcgt
ccccgccgcctctcaggagagctggtttacttcgagaagtctccggacttctgcgagcga
gaccctaccgtgggctcccccggcactcggggccgggcctgcaacaagaccagccggctg
ctcgatggctgtggcagcctgtgctgcggccgtgggcacaacatgctccggcagacacga
gttgagcgctgtcactgccgcttccactggtgctgctatgtgctgtgcgaggagtgcaag
gtcacggagtgggtcaacgtgtgtaagtga
DBGET
integrated database retrieval system