Equus asinus (ass): 106838461
Help
Entry
106838461 CDS
T04645
Symbol
WNT6
Name
(RefSeq) protein Wnt-6 isoform X3
KO
K00445
wingless-type MMTV integration site family, member 6
Organism
eai
Equus asinus (ass)
Pathway
eai04150
mTOR signaling pathway
eai04310
Wnt signaling pathway
eai04390
Hippo signaling pathway
eai04550
Signaling pathways regulating pluripotency of stem cells
eai04916
Melanogenesis
eai04934
Cushing syndrome
eai05010
Alzheimer disease
eai05022
Pathways of neurodegeneration - multiple diseases
eai05165
Human papillomavirus infection
eai05200
Pathways in cancer
eai05205
Proteoglycans in cancer
eai05217
Basal cell carcinoma
eai05224
Breast cancer
eai05225
Hepatocellular carcinoma
eai05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
eai00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
106838461 (WNT6)
04390 Hippo signaling pathway
106838461 (WNT6)
04150 mTOR signaling pathway
106838461 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
106838461 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
106838461 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
106838461 (WNT6)
05205 Proteoglycans in cancer
106838461 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
106838461 (WNT6)
05226 Gastric cancer
106838461 (WNT6)
05217 Basal cell carcinoma
106838461 (WNT6)
05224 Breast cancer
106838461 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
106838461 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
106838461 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
106838461 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
106838461 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
eai00536
]
106838461 (WNT6)
Glycosaminoglycan binding proteins [BR:
eai00536
]
Heparan sulfate / Heparin
Morphogens
106838461 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
106838461
NCBI-ProteinID:
XP_014708053
UniProt:
A0A8C4LX87
LinkDB
All DBs
Position
19:complement(19956229..19969976)
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
gtggtggctgagctggcccggggcgcccgactaggggtgcgagagtgccagttccagttt
cggttccgccgctggaactgctccagccacagcaaggccttcgggcgcatcctgcagcag
gacatccgggagacggccttcgtgttcgccataacggcggcgggtgccagccacgcggtc
acgcaggcctgctccatgggcgagctgctgcaatgcggctgccaggcgccccgggggcgc
gccccaccccgcccccctggcctgccaggcaccccggggccccctggccctgcgggctcc
ccggatggcagcgccgcctgggagtggggaggctgcggcgacgacgtggacttcggggat
gagaagtcgaggctctttatggatgcgcggcacaagcggggacgcggagacatccgtgca
ttggtgcagcttcacaacaacgaggcaggccggctggctgtgcggagccatacgcgcacc
gagtgcaagtgccacgggctgtcgggctcgtgcgcgctgcgcacctgctggcagaagctg
cccccgttccgcgaggtgggcgcgcggctgctcgagcgcttccacggtgcctcgcgtgtc
atgggcaccaacgacggcaaggctctgctgcccgccgtccgcactctcaagccgccgggc
cgcgccgacctgctctacgccgccgactcgcccgacttctgcgcccccaaccggcgcacc
ggctcgcccggcacgcgcggccgcgcctgcaacagcagtgccccggacctcagcggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagtgtgcagctcgaggagaactgc
ctgtgtcgcttccactggtgctgcgtagtgcagtgccaccgctgccgcgtgcacaaggag
ctcagcctctgcctctga
DBGET
integrated database retrieval system