KEGG   Galeopterus variegatus (Sunda flying lemur): 103598980
Entry
103598980         CDS       T08727                                 
Name
(RefSeq) protein Wnt-4
  KO
K00408  wingless-type MMTV integration site family, member 4
Organism
gvr  Galeopterus variegatus (Sunda flying lemur)
Pathway
gvr04150  mTOR signaling pathway
gvr04310  Wnt signaling pathway
gvr04360  Axon guidance
gvr04390  Hippo signaling pathway
gvr04550  Signaling pathways regulating pluripotency of stem cells
gvr04916  Melanogenesis
gvr04919  Thyroid hormone signaling pathway
gvr04934  Cushing syndrome
gvr05010  Alzheimer disease
gvr05022  Pathways of neurodegeneration - multiple diseases
gvr05165  Human papillomavirus infection
gvr05200  Pathways in cancer
gvr05205  Proteoglycans in cancer
gvr05217  Basal cell carcinoma
gvr05224  Breast cancer
gvr05225  Hepatocellular carcinoma
gvr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:gvr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    103598980
   04390 Hippo signaling pathway
    103598980
   04150 mTOR signaling pathway
    103598980
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103598980
 09150 Organismal Systems
  09152 Endocrine system
   04919 Thyroid hormone signaling pathway
    103598980
   04916 Melanogenesis
    103598980
  09158 Development and regeneration
   04360 Axon guidance
    103598980
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103598980
   05205 Proteoglycans in cancer
    103598980
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103598980
   05226 Gastric cancer
    103598980
   05217 Basal cell carcinoma
    103598980
   05224 Breast cancer
    103598980
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103598980
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103598980
   05022 Pathways of neurodegeneration - multiple diseases
    103598980
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103598980
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:gvr00536]
    103598980
Glycosaminoglycan binding proteins [BR:gvr00536]
 Heparan sulfate / Heparin
  Morphogens
   103598980
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 103598980
NCBI-ProteinID: XP_008581278
LinkDB
Position
Unknown
AA seq 230 aa
MCKRNLEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQAGAGKPPDQGA
VFTTLLGHSPLLCSQAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALKEKFDGA
TEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGTRGRTCNKTSK
AIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR
NT seq 693 nt   +upstreamnt  +downstreamnt
atgtgcaagcggaacctggaggtgatggactcagtgcgccgtggcgcccagctcgccatc
gaggagtgtcagtaccagttccggaaccggcgctggaactgctccaccctcgactctctg
cctgtcttcggcaaggtggtgactcaagctggggcaggcaaaccccctgaccagggagca
gtatttaccaccttgctggggcactccccgctgctctgctcccaggctatcctgacgcac
atgcgggtagagtgcaagtgccacggggtgtcgggctcctgtgaggtgaagacatgctgg
cgagccgtgccacccttccgccaggtgggccatgcgctgaaggagaagtttgatggcgcc
actgaggtggagccacgccgtgtgggctcctccagggcactggtgccacgcaacgcacag
ttcaagccacatacagatgaggacctggtgtacttggagcccagcccagacttctgcgaa
caggacatgcgcagtggcgtgctcggcacgaggggccgcacatgcaacaagacatccaag
gccattgacggctgtgagttgctatgctgtggccgtggcttccacacagcacaggtagag
ctggcagaacgctgcagttgcaaattccactggtgttgcttcgtcaagtgccggcagtgc
cagcggctcgtggagttgcacacgtgccgatga

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