Macaca mulatta (rhesus monkey): 696845
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Entry
696845 CDS
T01028
Symbol
WNT11
Name
(RefSeq) protein Wnt-11 isoform X2
KO
K01384
wingless-type MMTV integration site family, member 11
Organism
mcc
Macaca mulatta (rhesus monkey)
Pathway
mcc04150
mTOR signaling pathway
mcc04310
Wnt signaling pathway
mcc04390
Hippo signaling pathway
mcc04550
Signaling pathways regulating pluripotency of stem cells
mcc04916
Melanogenesis
mcc04934
Cushing syndrome
mcc05010
Alzheimer disease
mcc05022
Pathways of neurodegeneration - multiple diseases
mcc05165
Human papillomavirus infection
mcc05200
Pathways in cancer
mcc05205
Proteoglycans in cancer
mcc05217
Basal cell carcinoma
mcc05224
Breast cancer
mcc05225
Hepatocellular carcinoma
mcc05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
mcc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
696845 (WNT11)
04390 Hippo signaling pathway
696845 (WNT11)
04150 mTOR signaling pathway
696845 (WNT11)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
696845 (WNT11)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
696845 (WNT11)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
696845 (WNT11)
05205 Proteoglycans in cancer
696845 (WNT11)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
696845 (WNT11)
05226 Gastric cancer
696845 (WNT11)
05217 Basal cell carcinoma
696845 (WNT11)
05224 Breast cancer
696845 (WNT11)
09172 Infectious disease: viral
05165 Human papillomavirus infection
696845 (WNT11)
09164 Neurodegenerative disease
05010 Alzheimer disease
696845 (WNT11)
05022 Pathways of neurodegeneration - multiple diseases
696845 (WNT11)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
696845 (WNT11)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mcc00536
]
696845 (WNT11)
Glycosaminoglycan binding proteins [BR:
mcc00536
]
Heparan sulfate / Heparin
Morphogens
696845 (WNT11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
696845
NCBI-ProteinID:
XP_001086955
UniProt:
F7EV26
LinkDB
All DBs
Position
14:complement(69248135..69272542)
Genome browser
AA seq
354 aa
AA seq
DB search
MRARPQVCEALLFALALQTGICYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTVVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
TISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq
1065 nt
NT seq
+upstream
nt +downstream
nt
atgagggcgcggccgcaggtctgcgaggcgctgctcttcgccctggcgctccagaccggc
atatgctatggcatcaagtggctggcactgtccaagacaccagcagccctggcactgaac
cagacgcaacactgcaagcagctggagggcctggtgtctgcacaggtgcagctgtgccgc
agcaacctggagctcatgcacacggtggtgcacgctgcccgtgaggtcatgaaggcctgt
cgccgggccttcgccgacatgcgctggaactgctcctccatcgagctcgcccccaactat
ttgcttgacctggagagagggacccgggagtcggccttcgtgtatgcgctgtcggccgcc
accatcagccacgccatcgcccgggcctgcacctccggcgacctgccgggctgctcctgc
ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgcgcctctctggaaatgaagtgtaagtgccatggggtgtctggctcctgctccatc
cgcacctgctggaaggggctgcaggagctacgggatgtggctgctgacctcaagacccga
tacctgtcggccaccaaggtagtgcaccgacccatgggcacccgcaagcacctggtgccc
aaagacctggatatccggcctgtgaaggactcagaactcgtctatctgcagagctcacct
gacttctgcatgaagaatgagaaggtgggctcccacggaacacaagacaggcagtgcaac
aagacatccaatggaagtgacagctgcgatcttatgtgctgcgggcgtggctacaacccc
tacacagaccgcgtggtagagcggtgccactgtaagtaccactggtgctgctacgtcacc
tgccgcaggtgtgagcgtaccgtggagcgctatgtctgcaagtga
DBGET
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