Myotis brandtii (Brandt's bat): 102243634
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Entry
102243634 CDS
T02920
Symbol
WNT11
Name
(RefSeq) Wnt family member 11
KO
K01384
wingless-type MMTV integration site family, member 11
Organism
myb
Myotis brandtii (Brandt's bat)
Pathway
myb04150
mTOR signaling pathway
myb04310
Wnt signaling pathway
myb04390
Hippo signaling pathway
myb04550
Signaling pathways regulating pluripotency of stem cells
myb04916
Melanogenesis
myb04934
Cushing syndrome
myb05010
Alzheimer disease
myb05022
Pathways of neurodegeneration - multiple diseases
myb05165
Human papillomavirus infection
myb05200
Pathways in cancer
myb05205
Proteoglycans in cancer
myb05217
Basal cell carcinoma
myb05224
Breast cancer
myb05225
Hepatocellular carcinoma
myb05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
myb00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
102243634 (WNT11)
04390 Hippo signaling pathway
102243634 (WNT11)
04150 mTOR signaling pathway
102243634 (WNT11)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102243634 (WNT11)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102243634 (WNT11)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102243634 (WNT11)
05205 Proteoglycans in cancer
102243634 (WNT11)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102243634 (WNT11)
05226 Gastric cancer
102243634 (WNT11)
05217 Basal cell carcinoma
102243634 (WNT11)
05224 Breast cancer
102243634 (WNT11)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102243634 (WNT11)
09164 Neurodegenerative disease
05010 Alzheimer disease
102243634 (WNT11)
05022 Pathways of neurodegeneration - multiple diseases
102243634 (WNT11)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102243634 (WNT11)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
myb00536
]
102243634 (WNT11)
Glycosaminoglycan binding proteins [BR:
myb00536
]
Heparan sulfate / Heparin
Morphogens
102243634 (WNT11)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
102243634
NCBI-ProteinID:
XP_005867215
LinkDB
All DBs
Position
Un
AA seq
340 aa
AA seq
DB search
VALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCRSNLELMHTIVHAAR
EVMKACRRAFSDMRWNCSSIELAPNYLLDLERGTRESAFVYALSAATISHAIARACTSGD
LPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKKTGSQANKLMRLHNS
EVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVATDLKTRYLSATKVVHRPMGT
RKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCNKTSHGSDSCDLMCC
GRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq
1023 nt
NT seq
+upstream
nt +downstream
nt
gtggcgctgcagaccggcgtgtgctatggcatcaagtggctggcgctgtccaagacgccc
gcagccctggctctgaaccagacgcagcactgcaagcagctggagggcctggtgtccgca
caggtgcagctgtgccgcagcaacctggagctcatgcacaccatcgtgcacgccgcccga
gaggtcatgaaggcctgccgcagggccttctcggacatgcgctggaactgctcttccatc
gagctggcccccaactacctgcttgacctggagagagggacccgggagtccgccttcgtg
tatgcgctgtcagcagccaccatcagtcacgccatcgcccgggcctgcacctccggcgac
ctgcctggctgctcctgcggccctgtcccaggtgagccacccgggcccgggaaccgctgg
ggaggatgtgcggacaacctcagctacgggctcctcatgggggccaagttttccgatgct
cctatgaaggtgaaaaaaacaggatcccaagccaataaactgatgcgtctacacaacagt
gaagtggggagacaggctctgcgtgcgtctctggaaatgaagtgtaaatgccatggagta
tctggctcctgctccatccgcacctgctggaaggggctgcaggagcttcgggacgtggcc
actgacctgaagacccgctacctgtcggccaccaaggtagtgcaccgacccatgggcacc
cgcaagcacttggtgcccaaggacttggacattcggcctgtgaaggactcggagctcgtc
tatctgcagagctcacctgacttctgcatgaagaacgagaaggtgggctcccacgggaca
caagacaggcaatgcaacaagacatcccacggcagtgacagctgcgacctcatgtgctgt
ggacgcggctacaacccctacacggaccgcgtggtcgagcggtgccactgcaagtaccac
tggtgctgctacgtcacctgccgcaggtgtgagcgcacggtggagcgctacgtctgcaag
tga
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integrated database retrieval system