KEGG   Otolemur garnettii (small-eared galago): 100954223
Entry
100954223         CDS       T07855                                 
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
oga  Otolemur garnettii (small-eared galago)
Pathway
oga04150  mTOR signaling pathway
oga04310  Wnt signaling pathway
oga04390  Hippo signaling pathway
oga04550  Signaling pathways regulating pluripotency of stem cells
oga04916  Melanogenesis
oga04934  Cushing syndrome
oga05010  Alzheimer disease
oga05022  Pathways of neurodegeneration - multiple diseases
oga05165  Human papillomavirus infection
oga05200  Pathways in cancer
oga05205  Proteoglycans in cancer
oga05217  Basal cell carcinoma
oga05224  Breast cancer
oga05225  Hepatocellular carcinoma
oga05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:oga00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100954223 (WNT11)
   04390 Hippo signaling pathway
    100954223 (WNT11)
   04150 mTOR signaling pathway
    100954223 (WNT11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100954223 (WNT11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100954223 (WNT11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100954223 (WNT11)
   05205 Proteoglycans in cancer
    100954223 (WNT11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100954223 (WNT11)
   05226 Gastric cancer
    100954223 (WNT11)
   05217 Basal cell carcinoma
    100954223 (WNT11)
   05224 Breast cancer
    100954223 (WNT11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100954223 (WNT11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100954223 (WNT11)
   05022 Pathways of neurodegeneration - multiple diseases
    100954223 (WNT11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100954223 (WNT11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:oga00536]
    100954223 (WNT11)
Glycosaminoglycan binding proteins [BR:oga00536]
 Heparan sulfate / Heparin
  Morphogens
   100954223 (WNT11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100954223
NCBI-ProteinID: XP_003780934
Ensembl: ENSOGAG00000001568
UniProt: H0WIV9
LinkDB
Position
Unknown
AA seq 354 aa
MRARPQVCEALLFALALQTSMCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLDLMHTIVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEVKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq 1065 nt   +upstreamnt  +downstreamnt
atgagggcgcggccgcaggtctgcgaggcgctactcttcgccctagcgctccagaccagc
atgtgctatggcatcaagtggctggcactgtccaagactccggcggccctggcgctgaac
cagacgcaacactgcaagcagctggagggcctggtgtcagcacaggtgcagctgtgccgc
agcaacctggatctcatgcacaccatcgtgcatgccgcacgggaggtgatgaaggcctgc
cgcagggcctttgccgacatgcgctggaactgctcctccattgagctcgcccccaactac
ctgcttgacctggagagagggacccgggagtcagccttcgtgtatgcgctgtcggccgcc
gccatcagccacgccatcgcccgggcttgtacctccggtgacctgcccggctgctcctgc
ggccctgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgtgcctctctggaagtgaagtgcaagtgccacggggtatctggctcctgctccatc
cgcacctgctggaaggggctgcaggagctgcgggatgtagctgctgacctcaagacccgc
tacctctcagccaccaaggtagtgcaccgccccatgggcacccgcaaacacctggtgccc
aaggatctggatatccggcctgtgaaggactcagaacttgtatacctacagagttcgcct
gacttctgcatgaagaatgagaaagtgggctctcatgggacacaagacaggcagtgcaac
aagacatccaacggcagcgacagctgcgacctcatgtgctgtgggcgcggctacaacccc
tacacagaccgcgtggtcgagcggtgccactgcaagtaccactggtgctgctatgtcacc
tgccgcaggtgtgagcgcacagtggagcgctatgtctgcaagtga

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