Equus caballus (horse): 100064184
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Entry
100064184 CDS
T01058
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
KO
K01384
wingless-type MMTV integration site family, member 11
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
100064184 (WNT11)
04390 Hippo signaling pathway
100064184 (WNT11)
04150 mTOR signaling pathway
100064184 (WNT11)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100064184 (WNT11)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100064184 (WNT11)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100064184 (WNT11)
05205 Proteoglycans in cancer
100064184 (WNT11)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100064184 (WNT11)
05226 Gastric cancer
100064184 (WNT11)
05217 Basal cell carcinoma
100064184 (WNT11)
05224 Breast cancer
100064184 (WNT11)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100064184 (WNT11)
09164 Neurodegenerative disease
05010 Alzheimer disease
100064184 (WNT11)
05022 Pathways of neurodegeneration - multiple diseases
100064184 (WNT11)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100064184 (WNT11)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ecb00536
]
100064184 (WNT11)
Glycosaminoglycan binding proteins [BR:
ecb00536
]
Heparan sulfate / Heparin
Morphogens
100064184 (WNT11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
TarH
Motif
Other DBs
NCBI-GeneID:
100064184
NCBI-ProteinID:
XP_023501455
Ensembl:
ENSECAG00000022188
VGNC:
25043
LinkDB
All DBs
Position
7:70214469..70234793
Genome browser
AA seq
354 aa
AA seq
DB search
MRVRPQLCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMRTVVHAAREATKACRRAFSDMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTTGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSHGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq
1065 nt
NT seq
+upstream
nt +downstream
nt
atgagggtgcggccgcagctctgcgaggcgctgctcttcgccctggctctccagaccggc
gtgtgctacggcatcaaatggctggcgctgtccaagacgccggcggcgctggcgctgaac
cagacgcagcactgcaagcagctggagggcctggtgtcggcgcaggtgcagctgtgccgc
agcaacctggagctcatgcgcaccgtggtgcacgccgcccgcgaggccaccaaggcctgc
cgcagggccttctccgacatgcgctggaactgctcctccatagagctggcccccaactac
ctgcttgacctggagagagggacccgggagtccgccttcgtgtatgcgctgtctgcggct
gccatcagccacgccatcgcccgggcctgcaccaccggcgacctgcccggctgctcctgc
ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgcgcctctctggaaatgaagtgtaagtgccacggggtatccggctcctgctccatc
cgcacctgctggaaggggctgcaggagctacgggatgtggccgcagacctcaagacccgc
tacctgtcggccaccaaggtcgtgcaccgacccatgggcacccgcaagcacctggtgccc
aaggacctggacatccggcccgtgaaggactcggagctggtctatctgcagagctcccct
gacttctgcatgaagaacgagaaggtgggctcccacgggacacaggacaggcaatgcaac
aagacgtcccacggcagtgacagctgcgacctcatgtgctgtggccgtggctacaacccc
tacacggaccgcgtggtcgagcggtgccactgcaagtaccactggtgctgctacgtcacc
tgtcgccggtgtgagcgcaccgtggagcgctacgtgtgcaagtga
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integrated database retrieval system