Canis lupus familiaris (dog): 488528
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Entry
488528 CDS
T01007
Symbol
WNT10A
Name
(RefSeq) protein Wnt-10a
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
488528 (WNT10A)
04390 Hippo signaling pathway
488528 (WNT10A)
04150 mTOR signaling pathway
488528 (WNT10A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
488528 (WNT10A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
488528 (WNT10A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
488528 (WNT10A)
05205 Proteoglycans in cancer
488528 (WNT10A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
488528 (WNT10A)
05226 Gastric cancer
488528 (WNT10A)
05217 Basal cell carcinoma
488528 (WNT10A)
05224 Breast cancer
488528 (WNT10A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
488528 (WNT10A)
09164 Neurodegenerative disease
05010 Alzheimer disease
488528 (WNT10A)
05022 Pathways of neurodegeneration - multiple diseases
488528 (WNT10A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
488528 (WNT10A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
cfa00536
]
488528 (WNT10A)
Glycosaminoglycan binding proteins [BR:
cfa00536
]
Heparan sulfate / Heparin
Morphogens
488528 (WNT10A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
DUF7539
Ebola_NP
Motif
Other DBs
NCBI-GeneID:
488528
NCBI-ProteinID:
XP_545648
Ensembl:
ENSCAFG00000014987
VGNC:
48420
UniProt:
A0A8C0TSA8
A0A8I3QPH2
LinkDB
All DBs
Position
37:26283474..26295608
Genome browser
AA seq
417 aa
AA seq
DB search
MGSTHPCPRLRLRPRPQPRPALCALLFFLLLLAAAVPRSAPNDILGLRLPPEPVLNANTV
CLTLPGLSRRQMEVCVRHPDVAASAIQGIQIAIHECQHQFRDQRWNCSSLETRNKIPYES
PIFSRGFRESAFAYAIAAAGVVHAVSNACALGKLKACGCDASRRGDEEAFRRKLHRLQLD
ALQRGKGLSHGVPEHPALPPASPGLQDSWEWGGCSPDVGFGERFSKDFLDSREPHRDIHA
RMRLHNNRVGRQAVMENMRRKCKCHGTSGSCQLKTCWQVTPEFRAVGALLRSRFHRATLI
RPHNRNGGQLEPGPAGAPSPAPGAPGPRRRASPADLVYFEKSPDFCEREPRLDSAGTVGR
LCNKSSAGPDGCGSMCCGRGHNILRQTRSERCHCRFHWCCFVVCEECRITEWVSVCK
NT seq
1254 nt
NT seq
+upstream
nt +downstream
nt
atgggcagcacccacccttgcccccggctgcggctccgacctcggccccagccgcggccc
gcgctctgcgcgctcctgttcttcctactgctgctggctgccgccgtgcccaggtctgca
cccaacgacattctgggcctccgcctccccccggagcctgtgctcaatgccaacacggtg
tgcctaacgttgccgggcctgagcaggaggcagatggaagtgtgtgtgcgccacccagac
gtggctgcctcagccatccagggcatccagatcgccatccatgagtgccagcaccagttc
cgggaccagcgctggaactgctccagtctggagactcgcaacaagatcccctacgagagt
cccatcttcagcagaggttttcgcgagagcgccttcgcctatgccatcgcggcagctggg
gtcgtgcacgctgtgtccaatgcctgtgccctgggcaaactgaaggcctgcggctgtgat
gcctcccggcgcggggacgaggaggccttccgtcggaagctgcaccgcctgcagctggac
gcactgcagcgtggtaagggcttgagccacggggtcccggaacacccggccctgccccct
gccagccccggcctgcaggactcctgggagtggggcggctgtagccccgacgtgggcttc
ggggagcgcttctctaaggactttctggactcccgggagcctcacagagacatccacgca
cgcatgagactccacaacaaccgagttgggagacaggcggtgatggagaacatgcggcgg
aagtgcaagtgccacggcacgtcgggcagctgccagctcaagacgtgctggcaggtgacg
ccggagttccgcgcggtgggggcgctgctgcgcagccgcttccaccgcgccacgctcatc
cggccgcacaaccgcaacggcggccagctggagcccggccccgcgggggcgccctcgccg
gcccccggcgcccccggcccgcggcgccgcgccagccccgccgacctggtctacttcgag
aagtcgcccgacttctgcgagcgcgagccgcgcctggactcggcgggcaccgtgggccgc
ctgtgcaacaagagcagcgcgggccccgacggctgcggcagcatgtgctgcggccgcggc
cacaacatcctgcgccagacgcgcagcgagcgctgccactgccgcttccactggtgctgc
ttcgtggtgtgcgaggagtgccgcatcaccgagtgggtcagcgtgtgcaagtga
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