KEGG   Pipistrellus kuhlii (Kuhl's pipistrelle): 118730320
Entry
118730320         CDS       T07682                                 
Symbol
WNT1
Name
(RefSeq) proto-oncogene Wnt-1
  KO
K03209  wingless-type MMTV integration site family, member 1
Organism
pkl  Pipistrellus kuhlii (Kuhl's pipistrelle)
Pathway
pkl04150  mTOR signaling pathway
pkl04310  Wnt signaling pathway
pkl04390  Hippo signaling pathway
pkl04550  Signaling pathways regulating pluripotency of stem cells
pkl04916  Melanogenesis
pkl04934  Cushing syndrome
pkl05010  Alzheimer disease
pkl05022  Pathways of neurodegeneration - multiple diseases
pkl05165  Human papillomavirus infection
pkl05200  Pathways in cancer
pkl05205  Proteoglycans in cancer
pkl05207  Chemical carcinogenesis - receptor activation
pkl05217  Basal cell carcinoma
pkl05224  Breast cancer
pkl05225  Hepatocellular carcinoma
pkl05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pkl00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    118730320 (WNT1)
   04390 Hippo signaling pathway
    118730320 (WNT1)
   04150 mTOR signaling pathway
    118730320 (WNT1)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    118730320 (WNT1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    118730320 (WNT1)
   05205 Proteoglycans in cancer
    118730320 (WNT1)
   05207 Chemical carcinogenesis - receptor activation
    118730320 (WNT1)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    118730320 (WNT1)
   05226 Gastric cancer
    118730320 (WNT1)
   05217 Basal cell carcinoma
    118730320 (WNT1)
   05224 Breast cancer
    118730320 (WNT1)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    118730320 (WNT1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    118730320 (WNT1)
   05022 Pathways of neurodegeneration - multiple diseases
    118730320 (WNT1)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    118730320 (WNT1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pkl00536]
    118730320 (WNT1)
Glycosaminoglycan binding proteins [BR:pkl00536]
 Heparan sulfate / Heparin
  Morphogens
   118730320 (WNT1)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 118730320
NCBI-ProteinID: XP_036314091
LinkDB
Position
Unknown
AA seq 370 aa
MGHGALLPGWVSAALLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS
LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTASGPHLFGKIVNRG
CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF
GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR
AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT
YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC
THTRVLHECL
NT seq 1113 nt   +upstreamnt  +downstreamnt
atggggcacggggcgctgctgcccggctgggtttccgctgcgctgctgctggcgctggcc
gcgctgcccgccgctctggccgccaacagcagcggccgatggtggggcatcgtgaacgta
gcctcctccacgaacctcctgaccgactccaagagcctgcagctggtgctggagcccagc
ctgcagctgctgagccgcaagcagcggcggctgatccgccagaacccggggatcctgcac
agcgtgagtggggggctgcagagcgccgtgcgcgagtgcaagtggcagttccggaaccgc
cgctggaactgccccacagcctcggggccccacctcttcggcaagatcgtcaaccgaggc
tgtcgggaaacagcgtttatcttcgccatcacctccgccggcgtgacccactcggtggct
cgctcctgctccgagggctccatagagtcctgcacgtgcgactaccggcggcgcggcccc
ggcggccccgactggcactggggtggctgcagcgacaacatcgacttcggccgcctcttc
ggccgcgagtttgtggattccggggagaaggggcgggacctgcgcttcctcatgaacctt
cacaacaacgaggcgggccgcacgaccgtgttctccgagatgcgccaggagtgcaagtgc
cacggcatgtcgggctcgtgcacggtgcgcacgtgctggatgcggctgcccacgctgcgc
gccgtgggcgacgtgctgcgcgaccgcttcgacggcgcctcgcgcgtcctctacggcaac
cgcggcagcaaccgcgcctcgcgggccgagctgctccgcctcgagcccgaggaccccgcg
cacaagccgccctcgccccacgacctcgtctacttcgagaaatcgcccaacttctgcacg
tacagcgggcgcctgggcacggccggcaccgcggggcgcgcctgcaacagctcatcgccc
gcgctggacggctgcgagctgctctgctgcggccgcggccaccgcacccgcacgcagcgc
gtcacggagcgctgcaactgcaccttccactggtgctgccacgtcagctgccgcaactgc
acgcacacgcgcgtcctgcacgagtgtctgtga

DBGET integrated database retrieval system