KEGG   Echinops telfairi (small Madagascar hedgehog): 101656448
Entry
101656448         CDS       T08707                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
etf  Echinops telfairi (small Madagascar hedgehog)
Pathway
etf04150  mTOR signaling pathway
etf04310  Wnt signaling pathway
etf04390  Hippo signaling pathway
etf04550  Signaling pathways regulating pluripotency of stem cells
etf04916  Melanogenesis
etf04934  Cushing syndrome
etf05010  Alzheimer disease
etf05022  Pathways of neurodegeneration - multiple diseases
etf05165  Human papillomavirus infection
etf05200  Pathways in cancer
etf05205  Proteoglycans in cancer
etf05217  Basal cell carcinoma
etf05224  Breast cancer
etf05225  Hepatocellular carcinoma
etf05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:etf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101656448 (WNT7B)
   04390 Hippo signaling pathway
    101656448 (WNT7B)
   04150 mTOR signaling pathway
    101656448 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101656448 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    101656448 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101656448 (WNT7B)
   05205 Proteoglycans in cancer
    101656448 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101656448 (WNT7B)
   05226 Gastric cancer
    101656448 (WNT7B)
   05217 Basal cell carcinoma
    101656448 (WNT7B)
   05224 Breast cancer
    101656448 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101656448 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101656448 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    101656448 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101656448 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:etf00536]
    101656448 (WNT7B)
Glycosaminoglycan binding proteins [BR:etf00536]
 Heparan sulfate / Heparin
  Morphogens
   101656448 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 101656448
NCBI-ProteinID: XP_004700278
LinkDB
Position
Unknown
AA seq 353 aa
MLLLSSRSALLSVYCPQIFLILSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
EAIIVVGEGAQMGINECQHQFRFARWNCSALGERTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSSCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFRELGHLLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSFQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSQGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVRCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctgctgtcgtctcgcagcgcgctcctgtcggtctactgcccgcagatctttctc
atcctgtccagcggcagctacctagcgctgtcctccgtggtggccctgggagctaacatc
atctgcaacaagatccctggcttggccccgcggcagcgcgccatctgccagagtcgccct
gaggccatcatcgtggtcggcgagggcgcgcagatgggcatcaacgagtgccagcaccag
tttcgctttgcccgctggaactgctcggcgctgggcgagaggacggtcttcgggcaggag
ctccgagtaggaagccgagaagcggccttcacctacgccatcaccgcggccggcgtggcg
cacgccgtcaccgccgcctgcagccaaggcaacttgagcagctgcggctgcgaccgcgag
aagcagggctactacaaccaggcggagggctggaagtggggcggctgctccgccgacgtg
cgctacggcatcgacttctccaggcgcttcgtggatgcccgcgagatcaagaagaacgcg
cggcgactcatgaacctgcacaacaacgaggccggccgcaaggtcctggaggaacgcatg
aagctggagtgtaagtgtcacggcgtgtcgggctcgtgcaccaccaagacgtgctggacg
acgctgcccaaattccgcgagctgggccacctgctcaaggagaagtacaacgctgccgtg
caggtggaggtggtgcgcgccagccgcctgcggcagcccaccttcctgcgcatcaagcag
ctgcgcagcttccagaagcccatggagacggacctggtatacatcgagaagtcgcccaac
tactgcgaggaggacgcggccacgggcagcgtgggcacgcagggccgcctgtgcaaccgc
acctcgcaaggggccgacggctgcgacaccatgtgctgcggccgcggctacaacacgcac
caatacaccaaggtctggcagtgcaactgcaagttccactggtgctgtttcgtcaggtgc
aacacctgcagcgagcgcaccgaggtcttcacctgcaagtga

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