KEGG   Myotis yumanensis (Yuma myotis): 139018213
Entry
139018213         CDS       T10762                                 
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
  KO
K01384  wingless-type MMTV integration site family, member 11
Organism
myum  Myotis yumanensis (Yuma myotis)
Pathway
myum04150  mTOR signaling pathway
myum04310  Wnt signaling pathway
myum04390  Hippo signaling pathway
myum04550  Signaling pathways regulating pluripotency of stem cells
myum04916  Melanogenesis
myum04934  Cushing syndrome
myum05010  Alzheimer disease
myum05022  Pathways of neurodegeneration - multiple diseases
myum05165  Human papillomavirus infection
myum05200  Pathways in cancer
myum05205  Proteoglycans in cancer
myum05217  Basal cell carcinoma
myum05224  Breast cancer
myum05225  Hepatocellular carcinoma
myum05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:myum00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    139018213 (WNT11)
   04390 Hippo signaling pathway
    139018213 (WNT11)
   04150 mTOR signaling pathway
    139018213 (WNT11)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    139018213 (WNT11)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    139018213 (WNT11)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    139018213 (WNT11)
   05205 Proteoglycans in cancer
    139018213 (WNT11)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    139018213 (WNT11)
   05226 Gastric cancer
    139018213 (WNT11)
   05217 Basal cell carcinoma
    139018213 (WNT11)
   05224 Breast cancer
    139018213 (WNT11)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    139018213 (WNT11)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    139018213 (WNT11)
   05022 Pathways of neurodegeneration - multiple diseases
    139018213 (WNT11)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    139018213 (WNT11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:myum00536]
    139018213 (WNT11)
Glycosaminoglycan binding proteins [BR:myum00536]
 Heparan sulfate / Heparin
  Morphogens
   139018213 (WNT11)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 139018213
NCBI-ProteinID: XP_070282965
LinkDB
Position
Unknown
AA seq 354 aa
MRARPQVCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTIVHAAREVMKACRRAFSDMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
TISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVATDLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSHGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq 1065 nt   +upstreamnt  +downstreamnt
atgagggcgcggccgcaggtttgcgaggcgctgctcttcgccctggcgctgcagaccggc
gtgtgctatggcatcaagtggctggcgctgtccaagacgcccgcagccctggctctgaac
cagacgcagcactgcaagcagctggagggcctggtgtccgcgcaggtgcagctgtgtcgc
agcaacctggaactcatgcacaccatcgtgcacgccgcccgcgaggtcatgaaggcctgc
cgcagggccttctcggacatgcgctggaactgctcttccattgagctggcccccaactac
ctgcttgacctggagagagggacccgggagtccgccttcgtgtatgcgctgtcagcagcc
accatcagccacgccatcgcccgggcctgcacctccggcgacctgcctggctgctcctgc
ggccctgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgtgcgtctctggaaatgaagtgtaaatgccatggggtatctggctcctgctccatc
cgcacctgctggaaggggctgcaggagcttcgggacgtggccactgacctgaagacccgc
tacctgtcggccaccaaggtagtgcaccgacccatgggcacccgcaagcacttggtgccc
aaggacttggacattcggcctgtgaaggactcggagctcgtctatctgcagagctcacct
gacttctgcatgaagaacgagaaggtgggctcccacgggacgcaagacaggcaatgcaac
aagacatcccacggcagtgacagctgcgacctcatgtgctgtggacgcggctacaacccc
tacacagaccgcgtggtcgagcggtgccactgcaagtaccactggtgctgctacgtcacc
tgccgcaggtgtgagcgcacggtggagcgctacgtctgcaagtga

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