KEGG   Microcebus murinus (gray mouse lemur): 105860401
Entry
105860401         CDS       T07238                                 
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
mmur  Microcebus murinus (gray mouse lemur)
Pathway
mmur04150  mTOR signaling pathway
mmur04310  Wnt signaling pathway
mmur04390  Hippo signaling pathway
mmur04550  Signaling pathways regulating pluripotency of stem cells
mmur04916  Melanogenesis
mmur04934  Cushing syndrome
mmur05010  Alzheimer disease
mmur05022  Pathways of neurodegeneration - multiple diseases
mmur05165  Human papillomavirus infection
mmur05200  Pathways in cancer
mmur05205  Proteoglycans in cancer
mmur05217  Basal cell carcinoma
mmur05224  Breast cancer
mmur05225  Hepatocellular carcinoma
mmur05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mmur00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105860401 (WNT11)
   04390 Hippo signaling pathway
    105860401 (WNT11)
   04150 mTOR signaling pathway
    105860401 (WNT11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105860401 (WNT11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105860401 (WNT11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105860401 (WNT11)
   05205 Proteoglycans in cancer
    105860401 (WNT11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105860401 (WNT11)
   05226 Gastric cancer
    105860401 (WNT11)
   05217 Basal cell carcinoma
    105860401 (WNT11)
   05224 Breast cancer
    105860401 (WNT11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105860401 (WNT11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105860401 (WNT11)
   05022 Pathways of neurodegeneration - multiple diseases
    105860401 (WNT11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105860401 (WNT11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mmur00536]
    105860401 (WNT11)
Glycosaminoglycan binding proteins [BR:mmur00536]
 Heparan sulfate / Heparin
  Morphogens
   105860401 (WNT11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 105860401
NCBI-ProteinID: XP_012600597
Ensembl: ENSMICG00000015306
UniProt: A0A8B7F0K4
LinkDB
Position
5:complement(60737777..60758899)
AA seq 354 aa
MRARPQVCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTIVHAAREVTKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq 1065 nt   +upstreamnt  +downstreamnt
atgagggcgcggccgcaggtctgcgaggcgctgctcttcgccctggctctccagaccggc
gtgtgctatggcatcaagtggctggctctgtccaagacgccggcggccctggcgctgaac
cagacgcagcactgcaagcagctggagggcctggtgtccgcgcaggtgcagctgtgccgc
agcaacctggagctcatgcacaccatcgtgcacgccgcccgcgaggtgaccaaggcctgc
cgcagggccttcgccgacatgcgctggaactgctcctccatcgagctcgcccccaactac
ctgcttgacctggagagagggacccgggagtcggccttcgtgtatgcgctgtcggcagcc
gccatcagccacgccatcgcccgggcttgcacctccggcgacctgcccggctgctcctgc
ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgcgcctctctggaaatgaagtgcaagtgccatggggtgtctggctcctgctccatc
cgcacctgctggaaggggctgcaggagctgcgggacgtagctgctgacctcaagacccgc
tacctatcggccaccaaggtagtgcaccgacccatgggcacccgcaagcacctggtgccc
aaggatctggatatccggcctgtaaaggactcggaacttgtctacctgcagagttcgcct
gacttctgcatgaagaacgagaaggtgggctcccacgggacacaagacaggcagtgcaac
aagacatccaacggcagcgacagctgtgacctcatgtgctgtgggcgcggctacaacccc
tacacagaccgtgtggtcgagcggtgccactgcaagtaccactggtgctgctacgtcacc
tgccgcaggtgtgagcgcaccgtggagcgctacgtgtgcaagtga

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