Vulpes lagopus (Arctic fox): 121475935
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Entry
121475935 CDS
T07435
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
KO
K01384
wingless-type MMTV integration site family, member 11
Organism
vlg
Vulpes lagopus (Arctic fox)
Pathway
vlg04150
mTOR signaling pathway
vlg04310
Wnt signaling pathway
vlg04390
Hippo signaling pathway
vlg04550
Signaling pathways regulating pluripotency of stem cells
vlg04916
Melanogenesis
vlg04934
Cushing syndrome
vlg05010
Alzheimer disease
vlg05022
Pathways of neurodegeneration - multiple diseases
vlg05165
Human papillomavirus infection
vlg05200
Pathways in cancer
vlg05205
Proteoglycans in cancer
vlg05217
Basal cell carcinoma
vlg05224
Breast cancer
vlg05225
Hepatocellular carcinoma
vlg05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
vlg00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
121475935 (WNT11)
04390 Hippo signaling pathway
121475935 (WNT11)
04150 mTOR signaling pathway
121475935 (WNT11)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
121475935 (WNT11)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
121475935 (WNT11)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
121475935 (WNT11)
05205 Proteoglycans in cancer
121475935 (WNT11)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
121475935 (WNT11)
05226 Gastric cancer
121475935 (WNT11)
05217 Basal cell carcinoma
121475935 (WNT11)
05224 Breast cancer
121475935 (WNT11)
09172 Infectious disease: viral
05165 Human papillomavirus infection
121475935 (WNT11)
09164 Neurodegenerative disease
05010 Alzheimer disease
121475935 (WNT11)
05022 Pathways of neurodegeneration - multiple diseases
121475935 (WNT11)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
121475935 (WNT11)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
vlg00536
]
121475935 (WNT11)
Glycosaminoglycan binding proteins [BR:
vlg00536
]
Heparan sulfate / Heparin
Morphogens
121475935 (WNT11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
121475935
NCBI-ProteinID:
XP_041585538
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All DBs
Position
15:complement(27202272..27223721)
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AA seq
354 aa
AA seq
DB search
MRARPRVCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTIVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSHGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq
1065 nt
NT seq
+upstream
nt +downstream
nt
atgagggcgcggccgcgggtgtgcgaggcgctcctcttcgccctggcgctccagaccggc
gtgtgctacggcatcaaatggctggcgctgtccaagaccccggcggccctggcgctgaac
cagacgcagcactgcaagcagctggaggggctggtgtctgcgcaggtgcagctctgccgc
agcaacctggagcttatgcacaccatcgtgcacgctgcccgcgaggtcatgaaggcctgc
cgcagggcctttgcggacatgcgctggaactgctcctccatcgagcttgcccccaactac
ctgcttgacctggagagagggacccgggagtcggccttcgtgtatgcgctgtcggcggcc
gccatcagccacgccatcgcccgggcctgcacctccggggacctgcccggctgctcctgc
ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggcttctcatgggagccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgcgcctctctggaaatgaagtgtaagtgccatggggtatctggctcctgctccatc
cgcacctgctggaaggggctgcaggagcttcgggatgtggctgccgacctcaagacccgc
tacctgtcagccaccaaggtggtgcaccgccccatgggcacccgcaagcacctggtgccc
aaggacctggacatcaggcctgtgaaggactcagagcttgtctatctgcagagttcgccc
gacttctgcatgaagaacgagaaggtgggctcccacgggacgcaagacaggcagtgcaac
aaaacatcccatggcagtgacagctgtgacctcatgtgctgcggccgtggctacaaccct
tacacagaccgcgtggtcgagcgctgccactgcaagtatcactggtgctgctacgttacc
tgccgccgctgcgagcgcacagtggagcgctacgtttgcaagtga
DBGET
integrated database retrieval system