KEGG   Mastomys coucha (southern multimammate mouse): 116102613
Entry
116102613         CDS       T07224                                 
Symbol
Wnt11
Name
(RefSeq) protein Wnt-11 isoform X1
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
mcoc  Mastomys coucha (southern multimammate mouse)
Pathway
mcoc04150  mTOR signaling pathway
mcoc04310  Wnt signaling pathway
mcoc04390  Hippo signaling pathway
mcoc04550  Signaling pathways regulating pluripotency of stem cells
mcoc04916  Melanogenesis
mcoc04934  Cushing syndrome
mcoc05010  Alzheimer disease
mcoc05022  Pathways of neurodegeneration - multiple diseases
mcoc05165  Human papillomavirus infection
mcoc05200  Pathways in cancer
mcoc05205  Proteoglycans in cancer
mcoc05217  Basal cell carcinoma
mcoc05224  Breast cancer
mcoc05225  Hepatocellular carcinoma
mcoc05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mcoc00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    116102613 (Wnt11)
   04390 Hippo signaling pathway
    116102613 (Wnt11)
   04150 mTOR signaling pathway
    116102613 (Wnt11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    116102613 (Wnt11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    116102613 (Wnt11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    116102613 (Wnt11)
   05205 Proteoglycans in cancer
    116102613 (Wnt11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    116102613 (Wnt11)
   05226 Gastric cancer
    116102613 (Wnt11)
   05217 Basal cell carcinoma
    116102613 (Wnt11)
   05224 Breast cancer
    116102613 (Wnt11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    116102613 (Wnt11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    116102613 (Wnt11)
   05022 Pathways of neurodegeneration - multiple diseases
    116102613 (Wnt11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    116102613 (Wnt11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mcoc00536]
    116102613 (Wnt11)
Glycosaminoglycan binding proteins [BR:mcoc00536]
 Heparan sulfate / Heparin
  Morphogens
   116102613 (Wnt11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 116102613
NCBI-ProteinID: XP_031243337
LinkDB
Position
Unknown
AA seq 354 aa
MRARPQVCEALLFALALHTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMRTIVHAAREAMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
TISHTIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLETKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERMVERYVCK
NT seq 1065 nt   +upstreamnt  +downstreamnt
atgagggcgcggccgcaggtctgcgaggctctgctctttgccctggcgctccacaccggc
gtgtgctatggcatcaagtggctggcactgtccaagactccggcagccctggcactgaat
cagacacaacactgtaaacagctggagggcctggtgtctgcgcaggtgcagctctgccgc
agcaacctggagctcatgcgcaccatcgtgcatgctgcacgggaggccatgaaggcctgc
cgccgggccttcgctgacatgcgctggaactgctcctccattgagctcgcccccaactac
ctgcttgacctggagagaggtacccgggaatcagccttcgtgtatgccctgtctgccgcc
accatcagtcacaccatcgcccgggcctgcacctctggcgacctgcctggctgctcctgc
ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctacgtgcctccctggaaacgaagtgtaagtgccatggggtgtctggctcctgctccatc
cgcacctgttggaaggggctgcaagagctccgggatgtggctgctgacctcaagacccgc
tacctgtcagccacgaaggtggtacaccggcctatgggcacccgcaagcacttggtgccc
aaagacctggatatccggcctgtgaaggactcagaactcgtgtatctacagagttcccct
gacttctgcatgaagaatgagaaggtgggatcccatgggacccaagacaggcaatgcaac
aagacctccaacggcagtgacagctgcgacctcatgtgctgtgggcgcggctacaacccc
tacacggacagagtggtggagcgatgtcactgcaagtaccactggtgctgctatgtcacc
tgccgcaggtgtgagcgcatggtggagcgctatgtctgcaagtga

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