KEGG   Peromyscus leucopus (white-footed mouse): 114698691
Entry
114698691         CDS       T07241                                 
Symbol
Wnt11
Name
(RefSeq) protein Wnt-11 isoform X1
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
pleu  Peromyscus leucopus (white-footed mouse)
Pathway
pleu04150  mTOR signaling pathway
pleu04310  Wnt signaling pathway
pleu04390  Hippo signaling pathway
pleu04550  Signaling pathways regulating pluripotency of stem cells
pleu04916  Melanogenesis
pleu04934  Cushing syndrome
pleu05010  Alzheimer disease
pleu05022  Pathways of neurodegeneration - multiple diseases
pleu05165  Human papillomavirus infection
pleu05200  Pathways in cancer
pleu05205  Proteoglycans in cancer
pleu05217  Basal cell carcinoma
pleu05224  Breast cancer
pleu05225  Hepatocellular carcinoma
pleu05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pleu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    114698691 (Wnt11)
   04390 Hippo signaling pathway
    114698691 (Wnt11)
   04150 mTOR signaling pathway
    114698691 (Wnt11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    114698691 (Wnt11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    114698691 (Wnt11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    114698691 (Wnt11)
   05205 Proteoglycans in cancer
    114698691 (Wnt11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    114698691 (Wnt11)
   05226 Gastric cancer
    114698691 (Wnt11)
   05217 Basal cell carcinoma
    114698691 (Wnt11)
   05224 Breast cancer
    114698691 (Wnt11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    114698691 (Wnt11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    114698691 (Wnt11)
   05022 Pathways of neurodegeneration - multiple diseases
    114698691 (Wnt11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    114698691 (Wnt11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pleu00536]
    114698691 (Wnt11)
Glycosaminoglycan binding proteins [BR:pleu00536]
 Heparan sulfate / Heparin
  Morphogens
   114698691 (Wnt11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 114698691
NCBI-ProteinID: XP_028733320
LinkDB
Position
1:complement(106258812..106273525)
AA seq 354 aa
MRARPQVCEALLFALALHTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMRTVVYAAREAMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
TISHTIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLETKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq 1065 nt   +upstreamnt  +downstreamnt
atgagggcgcggccgcaggtctgcgaggctctgctcttcgccctggcgctccacaccggc
gtgtgctatggcatcaagtggctggcactgtccaagacgccagcggccctggccctcaac
cagacgcaacactgcaaacagctggagggcctggtgtctgcgcaggtgcagctgtgccgc
agcaacctggagctcatgcgcaccgtcgtgtacgcggcacgggaggccatgaaggcctgc
cgcagggccttcgccgacatgcgctggaactgctcctccatcgagctcgcccccaactac
ctgctcgacctggaaagaggtacccgggagtcagccttcgtgtatgccctgtcggccgcc
accatcagccacaccatcgcccgggcctgcacctctggcgacctgcccggctgctcctgc
ggccctgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggagccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctccgtgcctccctggaaacgaagtgtaagtgccatggggtgtctggctcctgctccatc
cgcacctgttggaaggggctccaggagctccgggatgtggctgctgacctcaagacccgc
tacctgtcagccaccaaagtggtgcaccgacctatgggtacccgcaagcacttggtgccc
aaggacctggatatccggcctgtgaaggactcagagctagtgtatctacagagctcccct
gacttctgtatgaagaacgagaaggtgggatcccacgggacccaagacaggcagtgcaac
aagacttccaacggcagtgacagctgcgacctcatgtgctgtgggcgtggctacaacccc
tacacagaccgagtggtggagaggtgccattgcaagtaccattggtgctgctacgtcacc
tgccgcaggtgtgagcgcacagtggagcgctacgtctgcaagtga

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