Mustela putorius furo (domestic ferret): 101692089
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Entry
101692089 CDS
T07239
Symbol
WNT6
Name
(RefSeq) protein Wnt-6
KO
K00445
wingless-type MMTV integration site family, member 6
Organism
mpuf
Mustela putorius furo (domestic ferret)
Pathway
mpuf04150
mTOR signaling pathway
mpuf04310
Wnt signaling pathway
mpuf04390
Hippo signaling pathway
mpuf04550
Signaling pathways regulating pluripotency of stem cells
mpuf04916
Melanogenesis
mpuf04934
Cushing syndrome
mpuf05010
Alzheimer disease
mpuf05022
Pathways of neurodegeneration - multiple diseases
mpuf05165
Human papillomavirus infection
mpuf05200
Pathways in cancer
mpuf05205
Proteoglycans in cancer
mpuf05217
Basal cell carcinoma
mpuf05224
Breast cancer
mpuf05225
Hepatocellular carcinoma
mpuf05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
mpuf00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
101692089 (WNT6)
04390 Hippo signaling pathway
101692089 (WNT6)
04150 mTOR signaling pathway
101692089 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
101692089 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
101692089 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
101692089 (WNT6)
05205 Proteoglycans in cancer
101692089 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
101692089 (WNT6)
05226 Gastric cancer
101692089 (WNT6)
05217 Basal cell carcinoma
101692089 (WNT6)
05224 Breast cancer
101692089 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
101692089 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
101692089 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
101692089 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
101692089 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mpuf00536
]
101692089 (WNT6)
Glycosaminoglycan binding proteins [BR:
mpuf00536
]
Heparan sulfate / Heparin
Morphogens
101692089 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
101692089
NCBI-ProteinID:
XP_004762845
Ensembl:
ENSMPUG00000016550
UniProt:
M3YYN7
LinkDB
All DBs
Position
Unknown
AA seq
365 aa
AA seq
DB search
MLPPAPSLLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPPGLPGTPGPPGPAGSPDGSAAWEWGGCGDDVDFGD
EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSTAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE
LSLCL
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgctgccgcccgcgccctccctcctcgggctgctgctgctgctcctcctgtgtcccgcg
cacgtcggtggactgtggtgggcggtgggcagccccctggtcatggaccccaccagcatc
tgcaggaaagcacggcggctggcaggacggcaagccgagctgtgccaggccgagccagaa
gtggtggcggagctagcccggggcgcccggcttggggtgcgagagtgccagttccagttc
cgtttccgccgctggaactgctccagccacagcaaggcctttgggcgcatcctgcagcag
gacatccgggagaccgccttcgtgtttgcgattactgctgcgggcgccagccacgcggtt
acgcaggcctgctctatgggtgagctgctgcagtgcggctgccaggcaccccgcgggcgg
gccccgccccgccccccgggtctgccgggcacccccgggcccccgggccccgccggctcc
cccgatggcagcgccgcctgggagtggggaggctgcggcgacgacgtggacttcggggac
gagaagtcgaggctcttcatggatgcgcggcacaagcggggtcgcggagacatccgtgcc
ttagtgcaacttcacaacaatgaggcgggccggctggccgtgcggagccatacgcgcacc
gagtgcaagtgtcacgggctgtcgggctcgtgcgcgctgcggacctgctggcagaagctg
cccccgttccgcgaggtgggcgcgcggctgctcgagcgcttccacggcgcctcgcgtgtt
atgggaaccaacgacggcaaggctctgctgcccgcggtccgcactctcaagccgcctggc
cgcgccgacctcctctacgcagccgactcgcccgacttctgcgctcccaacaggcgcacc
ggctcgcccggcacgcgtggccgcgcctgcaacagcaccgctccggacctcagcggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcaactcgaggagaactgc
ctgtgccgcttccattggtgctgcgtcgttcagtgccatcgctgtcgcgtgcgcaaggag
ctcagcctctgcctctga
DBGET
integrated database retrieval system