Mustela lutreola (European mink): 131827444
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Entry
131827444 CDS
T09578
Symbol
WNT6
Name
(RefSeq) protein Wnt-6
KO
K00445
wingless-type MMTV integration site family, member 6
Organism
mlk
Mustela lutreola (European mink)
Pathway
mlk04150
mTOR signaling pathway
mlk04310
Wnt signaling pathway
mlk04390
Hippo signaling pathway
mlk04550
Signaling pathways regulating pluripotency of stem cells
mlk04916
Melanogenesis
mlk04934
Cushing syndrome
mlk05010
Alzheimer disease
mlk05022
Pathways of neurodegeneration - multiple diseases
mlk05165
Human papillomavirus infection
mlk05200
Pathways in cancer
mlk05205
Proteoglycans in cancer
mlk05217
Basal cell carcinoma
mlk05224
Breast cancer
mlk05225
Hepatocellular carcinoma
mlk05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
mlk00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
131827444 (WNT6)
04390 Hippo signaling pathway
131827444 (WNT6)
04150 mTOR signaling pathway
131827444 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
131827444 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
131827444 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
131827444 (WNT6)
05205 Proteoglycans in cancer
131827444 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
131827444 (WNT6)
05226 Gastric cancer
131827444 (WNT6)
05217 Basal cell carcinoma
131827444 (WNT6)
05224 Breast cancer
131827444 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
131827444 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
131827444 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
131827444 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
131827444 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mlk00536
]
131827444 (WNT6)
Glycosaminoglycan binding proteins [BR:
mlk00536
]
Heparan sulfate / Heparin
Morphogens
131827444 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
131827444
NCBI-ProteinID:
XP_059024010
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All DBs
Position
3:complement(182537460..182551924)
Genome browser
AA seq
365 aa
AA seq
DB search
MLPPAPSLLRLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPSGLPGTPGPPGPAGSPDGSAAWEWGGCGDDVDFGD
EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSTAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE
LSLCL
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgctgccgcccgcgccctccctcctccggctgctgctgctgctgctcctgtgtcccgcg
cacgtcggtggactgtggtgggcggtgggcagccccctggtcatggaccccaccagcatc
tgcaggaaagcacggcggctggcaggacggcaagccgagctgtgccaggcggagccagaa
gtggtggcggagctagcccggggcgcccggcttggggtgcgagagtgccagttccagttc
cgtttccgccgctggaactgctccagccacagcaaggcctttgggcgcatcctgcagcag
gacatccgggagacggccttcgtgtttgcgattactgctgcgggcgccagccacgcggtt
acgcaggcctgctctatgggtgagctgctgcagtgcggctgccaggcaccccgcgggcgg
gccccgccccgcccctcgggtctgccgggcacccccgggcccccgggccccgccggctcc
cccgatggcagcgccgcctgggagtggggaggctgcggcgacgacgtggacttcggggac
gagaagtcgaggctcttcatggatgcgcggcacaagcggggtcgcggagacatccgtgcc
ttagtgcaacttcacaacaatgaggcgggccggctggccgtgcggagccatacgcgcacc
gagtgcaagtgtcacgggctgtcgggctcgtgcgcgctgcggacctgctggcagaagctg
cccccgttccgcgaggtgggcgcgcggctgctcgagcgcttccacggcgcctcgcgtgtt
atgggaaccaacgacggcaaggctctgctgcccgcggtccgcactctcaagccgcctggc
cgcgccgacctcctctacgcagccgactcgcccgacttctgcgctcccaacaggcgcacc
ggctcgcccggcacgcgtggccgcgcctgcaacagcaccgctccggacctcagcggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcaactcgaggagaactgc
ctgtgccgcttccattggtgctgcgtcgttcagtgccatcgctgtcgcgtgcgcaaggag
ctcagcctctgcctctga
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