Myotis davidii (David's myotis): 102757803
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Entry
102757803 CDS
T02992
Symbol
WNT6
Name
(RefSeq) Wnt family member 6
KO
K00445
wingless-type MMTV integration site family, member 6
Organism
myd
Myotis davidii (David's myotis)
Pathway
myd04150
mTOR signaling pathway
myd04310
Wnt signaling pathway
myd04390
Hippo signaling pathway
myd04550
Signaling pathways regulating pluripotency of stem cells
myd04916
Melanogenesis
myd04934
Cushing syndrome
myd05010
Alzheimer disease
myd05022
Pathways of neurodegeneration - multiple diseases
myd05165
Human papillomavirus infection
myd05200
Pathways in cancer
myd05205
Proteoglycans in cancer
myd05217
Basal cell carcinoma
myd05224
Breast cancer
myd05225
Hepatocellular carcinoma
myd05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
myd00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
102757803 (WNT6)
04390 Hippo signaling pathway
102757803 (WNT6)
04150 mTOR signaling pathway
102757803 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102757803 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102757803 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102757803 (WNT6)
05205 Proteoglycans in cancer
102757803 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102757803 (WNT6)
05226 Gastric cancer
102757803 (WNT6)
05217 Basal cell carcinoma
102757803 (WNT6)
05224 Breast cancer
102757803 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102757803 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
102757803 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
102757803 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102757803 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
myd00536
]
102757803 (WNT6)
Glycosaminoglycan binding proteins [BR:
myd00536
]
Heparan sulfate / Heparin
Morphogens
102757803 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
102757803
NCBI-ProteinID:
XP_015419174
LinkDB
All DBs
Position
Un
AA seq
347 aa
AA seq
DB search
MSVIYDPLKVIPTPPNLHQQEEGCKSCKVCKKADMFFDAAAEDLGAVGSPLVMDPTSICR
KARRLAGRQAELCQEEPEVVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQGQ
CEEGTSGLRGEGGGLGRLLEPHLSHKSLGTLPRPCLPAPPXPPGLVGSPEGSAAWEWGGC
GDDVDFGDEKSRLFMDARHKRGSGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCA
LRTCWQKLPPFREVGAELLERFHGASRVMGTNDGKALLPAVRNLKPPSRADLLYVADSPD
FCDLLCCGRGHREESVQLEENCLCRFHWCCVVQCHQCLVRKELSLCL
NT seq
1044 nt
NT seq
+upstream
nt +downstream
nt
atgtctgtcatctatgatcccttgaaagttattcccactcccccaaatctgcaccagcag
gaggagggctgtaaaagttgtaaggtctgcaagaaggcagatatgttctttgatgcagct
gcagaggatcttggggcagtgggcagccccttggtcatggaccccaccagtatctgcagg
aaagcacggaggctggcagggcggcaggctgagttgtgccaggaggagccggaagtggtg
gctgagctggcgcggggtgcccggcttggggttcgagagtgccagttccagttccgtttc
cgccgctggaactgctcgagccacagcaaggcctttgggcgcatcctgcagcagggtcag
tgtgaggagggaacctccgggctcagaggagagggtggaggtttggggaggctgctggag
ccccacctctcccacaaatctttgggcaccctgccccgaccctgtcttccagccccaccn
nngccccctggccttgtgggctccccagagggcagtgcagcctgggagtggggaggctgt
ggggacgatgtggacttcggggacgagaagtccaggctctttatggacgcgaggcataag
cggggaagtggagacatccgagcgttggtgcaacttcacaacaacgaggcgggccggctg
gcggtgcggagccacacgcgcactgaatgcaagtgccacggactgtcgggctcatgcgct
ctgcgcacctgctggcagaagctgcccccgttccgagaggtgggcgcggagctgctcgag
cgcttccacggcgcctcgcgtgtcatgggcaccaacgatggcaaggctctgctgcccgcg
gtccgcaatctcaagccgccgagtcgcgctgacctactctatgtcgccgactcgcccgac
ttctgcgacctgctgtgctgcggccgcgggcaccgcgaggagagcgtgcagctggaggag
aactgcctgtgccgcttccactggtgctgcgtagtgcagtgccaccagtgcctcgtgcgc
aaggagctcagcctctgcctctga
DBGET
integrated database retrieval system