KEGG   Rhinopithecus bieti (black snub-nosed monkey): 108527394
Entry
108527394         CDS       T04641                                 
Symbol
WNT11
Name
(RefSeq) protein Wnt-11 isoform X1
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
rbb  Rhinopithecus bieti (black snub-nosed monkey)
Pathway
rbb04150  mTOR signaling pathway
rbb04310  Wnt signaling pathway
rbb04390  Hippo signaling pathway
rbb04550  Signaling pathways regulating pluripotency of stem cells
rbb04916  Melanogenesis
rbb04934  Cushing syndrome
rbb05010  Alzheimer disease
rbb05022  Pathways of neurodegeneration - multiple diseases
rbb05165  Human papillomavirus infection
rbb05200  Pathways in cancer
rbb05205  Proteoglycans in cancer
rbb05217  Basal cell carcinoma
rbb05224  Breast cancer
rbb05225  Hepatocellular carcinoma
rbb05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:rbb00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    108527394 (WNT11)
   04390 Hippo signaling pathway
    108527394 (WNT11)
   04150 mTOR signaling pathway
    108527394 (WNT11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    108527394 (WNT11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    108527394 (WNT11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    108527394 (WNT11)
   05205 Proteoglycans in cancer
    108527394 (WNT11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    108527394 (WNT11)
   05226 Gastric cancer
    108527394 (WNT11)
   05217 Basal cell carcinoma
    108527394 (WNT11)
   05224 Breast cancer
    108527394 (WNT11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    108527394 (WNT11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    108527394 (WNT11)
   05022 Pathways of neurodegeneration - multiple diseases
    108527394 (WNT11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    108527394 (WNT11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:rbb00536]
    108527394 (WNT11)
Glycosaminoglycan binding proteins [BR:rbb00536]
 Heparan sulfate / Heparin
  Morphogens
   108527394 (WNT11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 108527394
NCBI-ProteinID: XP_017724120
LinkDB
Position
Unknown
AA seq 393 aa
MCPRSHGVGGESTALPAGTLGAFLGRSQETRRQSPLKAGVRRAVGGHVAPDNPVSPSIGH
GLSMVCRALSKTPAALALNQTQHCKQLEGLVSAQVQLCRSNLELMHTVVHAAREVMKACR
RAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAAAISHAIARACTSGDLPGCSCG
PVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKKTGSQANKLMRLHNSEVGRQAL
RASLEMKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTRYLSATKVVHRPMGTRKHLVPK
DLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCNKTSNGSDSCDLMCCGRGYNPY
TDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq 1182 nt   +upstreamnt  +downstreamnt
atgtgcccaaggtcacacggggtgggaggggagtccactgctctgccagctggcactttg
ggagcctttcttggaaggagccaggaaaccaggaggcaaagtccattgaaggctggggtc
agaagggcggttggaggccatgtggcccctgacaaccctgtctctccttccatcggtcat
ggcctttccatggtgtgcagggcactgtccaagacaccagcagccctggcactgaaccag
acacaacactgcaagcagctggagggcctggtgtctgcacaggtgcagctgtgccgcagc
aacctggagctcatgcacacggtggtgcacgctgcccgcgaggtcatgaaggcctgtcgc
cgggccttcgccgacatgcgctggaactgctcctccattgagctcgcccccaactatttg
cttgacctggagagagggacccgggagtcggccttcgtgtatgcgctgtcggccgccgcc
atcagccacgccatcgcccgggcctgcacctccggcgacctgccgggctgctcctgcggc
cccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaacctc
agctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaaaca
ggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggctctg
cgcgcctctctggaaatgaagtgtaagtgccatggggtgtctggctcctgctccatccgc
acctgctggaaggggctgcaggagctacgggatgtggctgctgacctcaagacccgatac
ctgtcggccaccaaggtagtgcaccgacccatgggcacccgcaagcacctggtgcccaaa
gacctggatatccggcctgtgaaggactcagaactcgtctacctgcagagctcacctgac
ttctgcatgaagaatgagaaggtgggctcccacggaacacaagacaggcagtgcaacaag
acatccaatggaagtgacagctgcgatcttatgtgctgtgggcgtggctacaacccctat
acagaccgcgtggtcgagcggtgccactgtaagtaccactggtgctgctacgtcacctgc
cgcaggtgtgagcgtaccgtggagcgctatgtctgcaagtga

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