Vulpes lagopus (Arctic fox): 121480717
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Entry
121480717 CDS
T07435
Symbol
WNT6
Name
(RefSeq) protein Wnt-6
KO
K00445
wingless-type MMTV integration site family, member 6
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
121480717 (WNT6)
04390 Hippo signaling pathway
121480717 (WNT6)
04150 mTOR signaling pathway
121480717 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
121480717 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
121480717 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
121480717 (WNT6)
05205 Proteoglycans in cancer
121480717 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
121480717 (WNT6)
05226 Gastric cancer
121480717 (WNT6)
05217 Basal cell carcinoma
121480717 (WNT6)
05224 Breast cancer
121480717 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
121480717 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
121480717 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
121480717 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
121480717 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
vlg00536
]
121480717 (WNT6)
Glycosaminoglycan binding proteins [BR:
vlg00536
]
Heparan sulfate / Heparin
Morphogens
121480717 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
121480717
NCBI-ProteinID:
XP_041593493
LinkDB
All DBs
Position
22:25554270..25567367
Genome browser
AA seq
365 aa
AA seq
DB search
MLPPAPSPLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPPGLPGTPGPPGPSGSPDGSATWEWGGCGDDVDFGD
EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE
LSLCL
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgctgccgcccgcgccctccccgctcgggctgctgctgctgctgctcctgtgccccgcg
cacgtcggtggactgtggtgggcggtgggcagccccctggtcatggaccctaccagcatc
tgcaggaaagcgcggcggctggcagggcggcaggctgagctgtgccaggctgagccagaa
gtggtggcggagctagcccggggcgcccggcttggggtgcgagagtgccagttccagttc
cgtttccgccgctggaactgttccagccacagcaaggccttcgggcgcatcctgcagcag
gacatccgggagacggcctttgtgtttgccatcacggctgcgggcgccagccacgcggtc
acgcaggcctgctccatgggggagctgctgcagtgcggctgccaggcgccccgcggccgg
gccccgcccaggccccctggcctgcctggcaccccggggcccccggggccctccggctcc
cccgatggcagcgccacctgggagtggggaggctgtggcgacgacgtggacttcggggac
gagaaatcaaggctctttatggatgcccggcacaagcggggtcgtggagacatccgtgca
ttggtgcaacttcacaacaatgaggcaggccgtctggccgtgcggagccacacgcgcacc
gagtgcaagtgccacgggctgtcgggctcgtgcgcgctgcgaacctgctggcagaagctg
cccccgttccgcgaggtgggcgcgcggctgctcgagcgcttccacggcgcctcgcgcgtc
atgggaaccaacgacggcaaggccctgctgcccgccgtccgcaccctgaagccgccgggc
cgcgccgacctcctctacgcagccgactcgcccgacttctgcgcgcccaaccggcgcacc
ggctctccgggcacgcgaggccgcgcgtgcaacagcagcgccccggacctcagcggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcagctcgaggagaactgc
ctgtgccgcttccactggtgctgcgtcgtgcagtgccaccgctgccgcgtgcgcaaggag
ctcagcctctgcctctga
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integrated database retrieval system