Equus caballus (horse): 100058824
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Entry
100058824 CDS
T01058
Symbol
WNT6
Name
(RefSeq) protein Wnt-6 isoform X1
KO
K00445
wingless-type MMTV integration site family, member 6
Organism
ecb
Equus caballus (horse)
Pathway
ecb04150
mTOR signaling pathway
ecb04310
Wnt signaling pathway
ecb04390
Hippo signaling pathway
ecb04550
Signaling pathways regulating pluripotency of stem cells
ecb04916
Melanogenesis
ecb04934
Cushing syndrome
ecb05010
Alzheimer disease
ecb05022
Pathways of neurodegeneration - multiple diseases
ecb05165
Human papillomavirus infection
ecb05200
Pathways in cancer
ecb05205
Proteoglycans in cancer
ecb05217
Basal cell carcinoma
ecb05224
Breast cancer
ecb05225
Hepatocellular carcinoma
ecb05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ecb00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100058824 (WNT6)
04390 Hippo signaling pathway
100058824 (WNT6)
04150 mTOR signaling pathway
100058824 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100058824 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100058824 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100058824 (WNT6)
05205 Proteoglycans in cancer
100058824 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100058824 (WNT6)
05226 Gastric cancer
100058824 (WNT6)
05217 Basal cell carcinoma
100058824 (WNT6)
05224 Breast cancer
100058824 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100058824 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
100058824 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
100058824 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100058824 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ecb00536
]
100058824 (WNT6)
Glycosaminoglycan binding proteins [BR:
ecb00536
]
Heparan sulfate / Heparin
Morphogens
100058824 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
100058824
NCBI-ProteinID:
XP_023498120
LinkDB
All DBs
Position
6:8224943..8237893
Genome browser
AA seq
365 aa
AA seq
DB search
MLPPAPSRLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPPGLPGTPGPPGPAGSPDGSAAWEWGGCGDDVDFGD
EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVHKE
LSLCL
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgctgccgcccgcgccctcccgcctcgggctgctgctgctgctgctcctgtgtccggcg
cacgtcggcggactgtggtgggccgtgggcagccccttggtcatggaccctaccagcatc
tgcaggaaggcacggcggctggcaggtcggcaggctgagttgtgccaggccgagccagaa
gtggtggctgagctggcccggggcgcccgactaggggtgcgagagtgccagttccagttc
cggttccgccgctggaactgctccagccacagcaaggccttcgggcgcatcctgcagcag
gacatccgggagacggccttcgtgttcgccataacggcggcgggtgccagccacgcggtc
acgcaggcctgctccatgggcgagctgctgcaatgcggctgccaggcgccccgggggcgc
gccccaccccgcccccctggcctgccaggcaccccggggccccctggccctgcgggctcc
ccggatggcagcgccgcctgggagtggggaggctgcggcgacgacgtggacttcggggat
gagaagtcgaggctctttatggatgcgcggcacaagcggggacgcggagacatccgtgca
ttggtgcagcttcacaacaacgaggcaggccggctggctgtgcggagccatacgcgcacc
gagtgcaagtgccacgggctgtcgggctcgtgcgcgctgcgcacctgctggcagaagctg
cccccgttccgcgaggtgggcgcgcggctgctcgagcgcttccacggtgcctcgcgtgtc
atgggcaccaacgacggcaaggctctgctgcccgccgtccgcactctcaagccgccgggc
cgcgccgacctgctctacgccgccgactcgcccgacttctgcgcccccaaccggcgcacc
ggctcgcccggcacgcgcggccgcgcctgcaacagcagtgccccggacctcagcggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagtgtgcagctcgaggagaactgc
ctgtgtcgcttccactggtgctgcgtagtgcagtgccaccgctgccgcgtgcacaaagag
ctcagcctctgcctctga
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