Ovis aries (sheep): 101111785
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Entry
101111785 CDS
T03117
Symbol
WNT6
Name
(RefSeq) protein Wnt-6 isoform X1
KO
K00445
wingless-type MMTV integration site family, member 6
Organism
oas
Ovis aries (sheep)
Pathway
oas04150
mTOR signaling pathway
oas04310
Wnt signaling pathway
oas04390
Hippo signaling pathway
oas04550
Signaling pathways regulating pluripotency of stem cells
oas04916
Melanogenesis
oas04934
Cushing syndrome
oas05010
Alzheimer disease
oas05022
Pathways of neurodegeneration - multiple diseases
oas05165
Human papillomavirus infection
oas05200
Pathways in cancer
oas05205
Proteoglycans in cancer
oas05217
Basal cell carcinoma
oas05224
Breast cancer
oas05225
Hepatocellular carcinoma
oas05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
oas00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
101111785 (WNT6)
04390 Hippo signaling pathway
101111785 (WNT6)
04150 mTOR signaling pathway
101111785 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
101111785 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
101111785 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
101111785 (WNT6)
05205 Proteoglycans in cancer
101111785 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
101111785 (WNT6)
05226 Gastric cancer
101111785 (WNT6)
05217 Basal cell carcinoma
101111785 (WNT6)
05224 Breast cancer
101111785 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
101111785 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
101111785 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
101111785 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
101111785 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
oas00536
]
101111785 (WNT6)
Glycosaminoglycan binding proteins [BR:
oas00536
]
Heparan sulfate / Heparin
Morphogens
101111785 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
101111785
NCBI-ProteinID:
XP_027820998
LinkDB
All DBs
Position
2:220834607..220847800
Genome browser
AA seq
365 aa
AA seq
DB search
MQPPAPSRLRLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPPGLPGTPGPPGPAGSPDGSAAWEWGGCGDDVDFGD
EKSRLFMDAQHKRGRGDIRMLVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVLLEENCLCRFHWCCVVQCHRCRVRKE
LSLCL
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgcagccgcccgcgccctcccgcctgcggctgctcctgctgctgctcctgtgtccggcg
cacgtcggcggactgtggtgggccgtgggcagccctttggtcatggaccctaccagcatc
tgcaggaaggcccggcggctcgcagggcggcaggctgagttgtgccaggccgagccagaa
gtggtggcagagctagcgcggggcgcccggctgggggttcgggaatgccagttccagttc
cgcttccgacgctggaactgctccagccatagcaaggccttcgggcgcatcctgcaacag
gacatccgggagacggccttcgtgttcgctataacggcggcgggcgccagccatgcggtc
acacaggcctgctccatgggcgagctgctgcagtgcggctgccaggcgccccgaggccgg
gccccaccccggccccccggcctgccaggcaccccagggccccccggccccgcggggtcc
cccgacggcagcgccgcctgggagtgggggggctgcggcgacgacgtggacttcggggac
gagaagtcgaggctcttcatggacgcgcagcacaaacggggacgtggagacatccgtatg
ttggtgcaacttcataacaacgaggcgggccggctggcggtgcggagccacacgcggacc
gaatgcaagtgccacggcctgtccggctcgtgcgcgctgcgcacctgctggcagaagctg
cccccgttccgcgaggtgggcgcgcggctgctcgagcggttccacggcgcctcgcgtgtc
atgggcaccaacgatggcaaggctctgctgcccgccgtccgcacgctcaagccgccgggc
cgcgctgacctgctctatgccgccgactcgcccgacttctgcgcccccaaccggcgcacg
ggttcgccgggcacccgcggccgcgcctgcaacagcagcgccccggacctcagcggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcttctcgaggagaactgc
ctgtgccgcttccactggtgctgcgtggtgcagtgccaccgctgccgcgtgcgcaaggag
ctcagcctttgcctttga
DBGET
integrated database retrieval system