KEGG   Cricetulus griseus (Chinese hamster): 100774690
Entry
100774690         CDS       T02813                                 
Symbol
Wnt11
Name
(RefSeq) protein Wnt-11 isoform X1
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
cge  Cricetulus griseus (Chinese hamster)
Pathway
cge04150  mTOR signaling pathway
cge04310  Wnt signaling pathway
cge04390  Hippo signaling pathway
cge04519  Cadherin signaling
cge04550  Signaling pathways regulating pluripotency of stem cells
cge04916  Melanogenesis
cge04934  Cushing syndrome
cge05010  Alzheimer disease
cge05022  Pathways of neurodegeneration - multiple diseases
cge05165  Human papillomavirus infection
cge05200  Pathways in cancer
cge05205  Proteoglycans in cancer
cge05217  Basal cell carcinoma
cge05224  Breast cancer
cge05225  Hepatocellular carcinoma
cge05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:cge00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100774690 (Wnt11)
   04390 Hippo signaling pathway
    100774690 (Wnt11)
   04150 mTOR signaling pathway
    100774690 (Wnt11)
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    100774690 (Wnt11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100774690 (Wnt11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100774690 (Wnt11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100774690 (Wnt11)
   05205 Proteoglycans in cancer
    100774690 (Wnt11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100774690 (Wnt11)
   05226 Gastric cancer
    100774690 (Wnt11)
   05217 Basal cell carcinoma
    100774690 (Wnt11)
   05224 Breast cancer
    100774690 (Wnt11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100774690 (Wnt11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100774690 (Wnt11)
   05022 Pathways of neurodegeneration - multiple diseases
    100774690 (Wnt11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100774690 (Wnt11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:cge00536]
    100774690 (Wnt11)
Glycosaminoglycan binding proteins [BR:cge00536]
 Heparan sulfate / Heparin
  Morphogens
   100774690 (Wnt11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100774690
NCBI-ProteinID: XP_035297243
UniProt: G3HUR9
LinkDB
Position
3:complement(100703962..100725616)
AA seq 354 aa
MRTRPQVCEALLFALALHTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMRTIVHAAREAMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
SISHTIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLETKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq 1065 nt   +upstreamnt  +downstreamnt
atgaggacgcggccgcaggtctgtgaggctctgctcttcgccctggcgctccacactggc
gtgtgctatggcatcaagtggctggcactgtccaagacgccagcagccctggcactcaac
cagacacaacactgcaaacagctggaaggcctggtgtctgcgcaggtgcagctctgccgc
agcaacctggagctcatgcgtaccatcgtgcacgcagcacgggaggccatgaaggcctgc
cgcagggccttcgctgacatgcgctggaattgctcctccatcgagcttgctcccaactac
ctgcttgacctggagagaggtacccgggagtcagccttcgtgtatgccctgtcggccgcc
agcatcagccacaccatcgcccgggcctgcacctctggcgacctgcccggctgctcctgc
ggccctgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcggctacacaacagtgaagtggggagacaggct
ctacgtgcctccctggaaacgaagtgtaagtgccatggggtgtctggctcctgctccatc
cgcacctgttggaaggggctgcaagagctccgggatgtggctgctgacctcaagacccgc
tacctttcggccacaaaagtggtgcaccggcctatgggcacccgcaagcacttggtgccc
aaggacctggatattaggcctgtgaaggactcagaactagtatatctgcagagctcccct
gacttctgtatgaagaacgagaaagtgggatcccatgggacccaagacaggcagtgcaac
aagacctcaaatggcagtgacagctgcgacctcatgtgctgtgggcgcggctacaacccc
tacacggaccgagtggtggagcgatgccactgcaagtaccattggtgctgctatgtcacc
tgccgcaggtgtgagcgcacagtggagcgctatgtctgcaagtga

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