KEGG   Galeopterus variegatus (Sunda flying lemur): 103609951
Entry
103609951         CDS       T08727                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
gvr  Galeopterus variegatus (Sunda flying lemur)
Pathway
gvr04150  mTOR signaling pathway
gvr04310  Wnt signaling pathway
gvr04390  Hippo signaling pathway
gvr04550  Signaling pathways regulating pluripotency of stem cells
gvr04916  Melanogenesis
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
    103609951 (WNT7B)
   04390 Hippo signaling pathway
    103609951 (WNT7B)
   04150 mTOR signaling pathway
    103609951 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103609951 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    103609951 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103609951 (WNT7B)
   05205 Proteoglycans in cancer
    103609951 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103609951 (WNT7B)
   05226 Gastric cancer
    103609951 (WNT7B)
   05217 Basal cell carcinoma
    103609951 (WNT7B)
   05224 Breast cancer
    103609951 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103609951 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103609951 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    103609951 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103609951 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:gvr00536]
    103609951 (WNT7B)
Glycosaminoglycan binding proteins [BR:gvr00536]
 Heparan sulfate / Heparin
  Morphogens
   103609951 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 103609951
NCBI-ProteinID: XP_008592426
LinkDB
Position
Unknown
AA seq 282 aa
MGINECQYQFRFGRWNCSALGERTVFGQELRVGSREAAFTYAITAAGVAHAVTAACSQGN
LSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNARRLMNLHNNEA
GRKVLEDRMKLECKCHGVSGSCTTKTCWTTLPKFREVGHQLKEKYNAAVQVEVVRASRLR
QPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTSPGADGCDTM
CCGRGYNTHQYTKVWQCNCKFHWCCFVRCSTCSERTEVFTCK
NT seq 849 nt   +upstreamnt  +downstreamnt
atgggcatcaacgagtgccagtaccagttccgcttcggccgctggaactgctccgccctc
ggtgagaggaccgtcttcgggcaagagctccgagtagggagccgtgaggccgccttcacc
tacgccatcaccgcggcgggcgtggcccacgccgtcaccgccgcctgcagccagggcaac
ctgagcaactgcggctgcgaccgcgagaagcagggctactacaaccaggccgagggctgg
aagtggggcggctgctccgccgacgtgcgctacggcatcgacttctcccggcgcttcgtg
gacgcgcgcgagatcaagaagaacgcgcggcgcctcatgaacctgcacaacaacgaggcg
ggcaggaaggttctggaggaccgcatgaagctggagtgcaagtgccacggcgtgtcgggc
tcgtgcaccaccaagacctgctggaccacgctgcccaagttccgcgaggtgggccaccag
ctcaaggagaagtacaacgcggccgtgcaggtggaggtggtgcgggccagccgcctgcgg
cagcccaccttcctacgcatcaagcagctgcgcagctaccagaagcccatggagacggac
ctggtgtacatcgagaagtcgcccaactactgtgaggaggacgcggccacgggcagcgtg
ggcacgcagggccgcctgtgcaaccgcacctcacccggtgccgacggctgtgacaccatg
tgctgcggccgcggctacaacacccaccagtacaccaaggtctggcagtgcaactgcaag
ttccactggtgctgcttcgtcaggtgcagcacgtgcagcgagcgcaccgaggtcttcacc
tgcaagtga

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