Vicugna pacos (alpaca): 102536488
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Entry
102536488 CDS
T08098
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
KO
K01384
wingless-type MMTV integration site family, member 11
Organism
vpc
Vicugna pacos (alpaca)
Pathway
vpc04150
mTOR signaling pathway
vpc04310
Wnt signaling pathway
vpc04390
Hippo signaling pathway
vpc04550
Signaling pathways regulating pluripotency of stem cells
vpc04916
Melanogenesis
vpc04934
Cushing syndrome
vpc05010
Alzheimer disease
vpc05022
Pathways of neurodegeneration - multiple diseases
vpc05165
Human papillomavirus infection
vpc05200
Pathways in cancer
vpc05205
Proteoglycans in cancer
vpc05217
Basal cell carcinoma
vpc05224
Breast cancer
vpc05225
Hepatocellular carcinoma
vpc05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
vpc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
102536488 (WNT11)
04390 Hippo signaling pathway
102536488 (WNT11)
04150 mTOR signaling pathway
102536488 (WNT11)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102536488 (WNT11)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102536488 (WNT11)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102536488 (WNT11)
05205 Proteoglycans in cancer
102536488 (WNT11)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102536488 (WNT11)
05226 Gastric cancer
102536488 (WNT11)
05217 Basal cell carcinoma
102536488 (WNT11)
05224 Breast cancer
102536488 (WNT11)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102536488 (WNT11)
09164 Neurodegenerative disease
05010 Alzheimer disease
102536488 (WNT11)
05022 Pathways of neurodegeneration - multiple diseases
102536488 (WNT11)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102536488 (WNT11)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
vpc00536
]
102536488 (WNT11)
Glycosaminoglycan binding proteins [BR:
vpc00536
]
Heparan sulfate / Heparin
Morphogens
102536488 (WNT11)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
102536488
NCBI-ProteinID:
XP_031537222
UniProt:
A0A6J3AVL6
LinkDB
All DBs
Position
10
AA seq
262 aa
AA seq
DB search
MRTRPQVCQALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTIVHAAREAMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTSGDLQELRDVATDLKTRYLSATKVVHRPMGTRKHLVPKDLDIRPVKDSE
LVYLQSSPDFCMKNEKVGSHGTQDRQCNKTSHGSDSCDLMCCGRGYNPYTDRVVERCHCK
YHWCCYVTCRRCERTVERYVCK
NT seq
789 nt
NT seq
+upstream
nt +downstream
nt
atgaggacgcggccgcaggtctgccaggcgcttctcttcgccctggcgctccagaccggc
gtgtgctatggcatcaagtggctggcgctgtccaagaccccggcggccctggcgctgaac
cagacacagcactgcaaacagctggagggcctggtgtcggcgcaggtgcagctgtgccgc
agcaacctggagctcatgcacaccatcgtgcacgccgcccgcgaggccatgaaggcctgc
cgcagggccttcgctgacatgcgctggaactgctcctccatcgagctcgcccccaactac
ctgcttgacctggagagagggacccgggagtcagccttcgtgtatgcgctgtcggcggcc
gccatcagccacgccatcgcccgggcctgcacctccggcgacctgcaggagctccgggat
gtggccactgaccttaagacccgctacctgtcggccaccaaggtggtgcaccgacctatg
ggcacccgcaagcacctagtgcccaaggacctggacattcggcccgtgaaggactcggag
ctcgtctatctgcagagctcccccgacttctgcatgaagaacgagaaggtgggctctcac
gggacgcaggacaggcagtgcaacaagacatcacatggcagcgacagctgtgacctcatg
tgctgtggacgcggctacaacccctacacagaccgcgtggtggagcggtgccactgcaag
taccactggtgctgctatgtcacctgccgcaggtgtgagcgcaccgtggagcgctatgtc
tgcaagtga
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integrated database retrieval system