Equus caballus (horse): 100063730
Help
Entry
100063730 CDS
T01058
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
KO
K01064
wingless-type MMTV integration site family, member 9
Organism
ecb
Equus caballus (horse)
Pathway
ecb04150
mTOR signaling pathway
ecb04310
Wnt signaling pathway
ecb04390
Hippo signaling pathway
ecb04550
Signaling pathways regulating pluripotency of stem cells
ecb04916
Melanogenesis
ecb04934
Cushing syndrome
ecb05010
Alzheimer disease
ecb05022
Pathways of neurodegeneration - multiple diseases
ecb05165
Human papillomavirus infection
ecb05200
Pathways in cancer
ecb05205
Proteoglycans in cancer
ecb05217
Basal cell carcinoma
ecb05224
Breast cancer
ecb05225
Hepatocellular carcinoma
ecb05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ecb00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100063730 (WNT9B)
04390 Hippo signaling pathway
100063730 (WNT9B)
04150 mTOR signaling pathway
100063730 (WNT9B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100063730 (WNT9B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100063730 (WNT9B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100063730 (WNT9B)
05205 Proteoglycans in cancer
100063730 (WNT9B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100063730 (WNT9B)
05226 Gastric cancer
100063730 (WNT9B)
05217 Basal cell carcinoma
100063730 (WNT9B)
05224 Breast cancer
100063730 (WNT9B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100063730 (WNT9B)
09164 Neurodegenerative disease
05010 Alzheimer disease
100063730 (WNT9B)
05022 Pathways of neurodegeneration - multiple diseases
100063730 (WNT9B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100063730 (WNT9B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ecb00536
]
100063730 (WNT9B)
Glycosaminoglycan binding proteins [BR:
ecb00536
]
Heparan sulfate / Heparin
Morphogens
100063730 (WNT9B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
100063730
NCBI-ProteinID:
XP_014595072
Ensembl:
ENSECAG00000011600
VGNC:
25052
LinkDB
All DBs
Position
11:18205804..18215204
Genome browser
AA seq
378 aa
AA seq
DB search
MEIEGTVKPLRRPPSPHLPHVHRDCHPSSSLSQPLKVTGLPPLALSSLTGREVLTPFPGL
GTAAAPAQGGAHLKQCDLLKLSRRQKQLCRREPGLAETLQEAAHLSLLECQFQFRHERWN
CSLEGRTALLKRGFKETAFLYAVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQW
GVCGDNLKYSTKFLSNFLGPKRGSKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSC
AVRTCWKQLSPFREMGQVLKLRYDSAVKVSSATNEALGRLELWAPARPGSPNKGLAPRPG
DLVYMEDSPSFCRPSKYSPGTAGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCC
YVECQQCVQEELVYTCKH
NT seq
1137 nt
NT seq
+upstream
nt +downstream
nt
atggagatagaaggaacagtgaagcctctgagaaggcccccttctcctcacctgccccat
gtccacagggattgtcatccttcgtcttccctgtcacaacccctaaaggtcactggtctc
ccccctctcgccctctctagcctgactgggcgggaggtcctgacgcccttcccagggctg
ggcaccgccgcggccccggcgcagggtggggcccacctgaagcagtgtgacctgctgaag
ctgtcccgccggcagaagcagctctgtcgacgggagccgggcctggcggagacgctgcag
gaggccgcgcacctcagcctgctcgagtgccagttccagttccgccacgagcgctggaac
tgcagcctggaggggaggacggccctgctcaagagaggtttcaaggagacagccttcctg
tatgcagtgtcctcggccgccctcacgcacactttggcccgggcctgcagcgctgggcgc
atggagcgctgcacctgcgatgactctccaggcctggagagccggcaggcctggcagtgg
ggcgtgtgcggcgacaacctcaagtacagcaccaagttcctgagcaacttcctggggccc
aagagaggaagcaaggacctgcgggcacgggcagatgcccacaacacccacgtgggcatc
aaggccgtgaagagtggcctcaggaccacgtgtaagtgccacggtgtgtccggctcctgc
gccgtgcgcacctgctggaagcagctgtccccattccgcgagatgggccaggtgctgaag
ctgcgctacgactcagctgtcaaggtgtccagtgccaccaatgaggccttgggccgcctg
gagttgtgggcacccgccaggccgggcagccccaacaagggcctggccccccggcctggg
gaccttgtctacatggaggactcacccagtttctgccggcccagcaagtactcgccaggc
acggcgggcagggtgtgctcccgggaggccagctgcagcagcctgtgctgcgggcggggc
tatgacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgc
tatgtggagtgccagcagtgcgtgcaggaggagctcgtgtacacctgcaagcactag
DBGET
integrated database retrieval system
