KEGG   Ursus arctos horribilis (North American brown bear): 113269338
Entry
113269338         CDS       T05909                                 
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
uah  Ursus arctos horribilis (North American brown bear)
Pathway
uah04150  mTOR signaling pathway
uah04310  Wnt signaling pathway
uah04390  Hippo signaling pathway
uah04550  Signaling pathways regulating pluripotency of stem cells
uah04916  Melanogenesis
uah04934  Cushing syndrome
uah05010  Alzheimer disease
uah05022  Pathways of neurodegeneration - multiple diseases
uah05165  Human papillomavirus infection
uah05200  Pathways in cancer
uah05205  Proteoglycans in cancer
uah05217  Basal cell carcinoma
uah05224  Breast cancer
uah05225  Hepatocellular carcinoma
uah05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:uah00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    113269338 (WNT11)
   04390 Hippo signaling pathway
    113269338 (WNT11)
   04150 mTOR signaling pathway
    113269338 (WNT11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    113269338 (WNT11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    113269338 (WNT11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    113269338 (WNT11)
   05205 Proteoglycans in cancer
    113269338 (WNT11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    113269338 (WNT11)
   05226 Gastric cancer
    113269338 (WNT11)
   05217 Basal cell carcinoma
    113269338 (WNT11)
   05224 Breast cancer
    113269338 (WNT11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    113269338 (WNT11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    113269338 (WNT11)
   05022 Pathways of neurodegeneration - multiple diseases
    113269338 (WNT11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    113269338 (WNT11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:uah00536]
    113269338 (WNT11)
Glycosaminoglycan binding proteins [BR:uah00536]
 Heparan sulfate / Heparin
  Morphogens
   113269338 (WNT11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 113269338
NCBI-ProteinID: XP_026373913
LinkDB
Position
Unknown
AA seq 354 aa
MRARPRVCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTIVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEVKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSHGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq 1065 nt   +upstreamnt  +downstreamnt
atgagggcgcggccgcgggtctgcgaggcgctcctcttcgccctggctctccagaccggc
gtgtgctacggcatcaaatggctggcgctgtccaagaccccggcggccctcgcgctgaac
cagacgcagcactgcaagcagctggaggggctggtgtcggcgcaggtgcagctctgccgc
agcaacctggagctcatgcacaccatcgtgcacgccgcccgcgaggtcatgaaggcctgc
cgcagggcctttgcggacatgcgctggaactgttcctccatcgagcttgcccccaactac
ctgcttgacctggagagagggacccgggagtcagccttcgtgtatgcgttgtcggcggcc
gccatcagccacgccatcgcccgggcctgcacctccggcgacctgcccggctgctcctgc
ggccctgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgcgcctctctggaggtgaagtgtaagtgccacggcgtgtccggctcctgctccatc
cgcacctgctggaaggggctgcaggagctccgggacgtggctgccgacctcaagacccgc
tacctgtcggccaccaaggtggtgcaccgacccatgggcacccgcaagcacctggtgccc
aaggacctggatatcaggcctgtgaaggactcggagcttgtctatctgcagagctcccct
gacttctgcatgaagaacgagaaggtgggctcccatgggacgcaagacaggcagtgcaac
aagacgtcccacggcagtgacagctgtgacctcatgtgctgcggccgtggctacaacccc
tacacggaccgcgtggtcgagcgctgccactgcaagtatcactggtgctgctacgtcacg
tgccgccgctgcgagcgcacggtggagcgctacgtctgcaagtga

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