KEGG   Suncus etruscus (white-toothed pygmy shrew): 126006279
Entry
126006279         CDS       T09902                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
setr  Suncus etruscus (white-toothed pygmy shrew)
Pathway
setr04150  mTOR signaling pathway
setr04310  Wnt signaling pathway
setr04390  Hippo signaling pathway
setr04550  Signaling pathways regulating pluripotency of stem cells
setr04916  Melanogenesis
setr04934  Cushing syndrome
setr05010  Alzheimer disease
setr05022  Pathways of neurodegeneration - multiple diseases
setr05165  Human papillomavirus infection
setr05200  Pathways in cancer
setr05205  Proteoglycans in cancer
setr05217  Basal cell carcinoma
setr05224  Breast cancer
setr05225  Hepatocellular carcinoma
setr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:setr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    126006279 (WNT7B)
   04390 Hippo signaling pathway
    126006279 (WNT7B)
   04150 mTOR signaling pathway
    126006279 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    126006279 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    126006279 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    126006279 (WNT7B)
   05205 Proteoglycans in cancer
    126006279 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    126006279 (WNT7B)
   05226 Gastric cancer
    126006279 (WNT7B)
   05217 Basal cell carcinoma
    126006279 (WNT7B)
   05224 Breast cancer
    126006279 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    126006279 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    126006279 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    126006279 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    126006279 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:setr00536]
    126006279 (WNT7B)
Glycosaminoglycan binding proteins [BR:setr00536]
 Heparan sulfate / Heparin
  Morphogens
   126006279 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973 DUF7259
Other DBs
NCBI-GeneID: 126006279
NCBI-ProteinID: XP_049627618
LinkDB
Position
4:1689025..1715370
AA seq 353 aa
MLLQRRRRALLSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGIDECQHQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYSGQADGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYHAAV
QVEVVRASRLRQPTFLRVKQLRSFQKPLETDLVYIDKSPNYCEEDAATGSVGTRGRLCNR
TSPGGDGCHTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVYTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctgcagagaaggcggcgcgcgctcctgtccgtctactgcccgcagatcttcctc
ctgctgtccagcggcagttacctggcactgtcgtccgtggtggcgctgggcgccaacatc
atctgtaacaagatcccgggcctggccccgcggcagcgtgccatctgccagagccggccg
gacgccatcatcgtcatcggggagggggcacagatgggcatcgacgagtgtcagcaccag
ttccgcttcggccgctggaactgctcggccctgggcgagaagacggtcttcgggcaggag
ctgcgagtagggagccgcgaggccgccttcacctatgccatcaccgcggcaggcgtggcc
cacgccgtcacggccgcctgcagccaagggaacctgagcaactgcggctgcgaccgggag
aagcaaggctactcgggccaggcggacggctggaagtggggcggctgctcggccgacgtg
cgctacggcattgacttctcccgccgcttcgtggacgcgagggagatcaagaagaacgcg
cggcgcctcatgaacctgcacaacaacgaggcgggcaggaaggtgctggaggagcgcatg
aagctggagtgcaagtgccacggcgtgtcgggctcctgcaccaccaagacgtgctggacc
acgctgcccaagttccgcgaggtgggccacctgctcaaggagaagtaccacgcggccgtg
caggtggaggtggtgcgcgccagccgcctgcgccagcccaccttcctgcgcgtcaagcag
ctgcgcagcttccagaagccgctggagacggacctggtgtacatcgacaagtcgcccaac
tactgcgaggaggacgcggccacgggcagcgtgggcacgcgcggccgcctgtgcaaccgc
acctcgcccggcggcgacggctgccacaccatgtgctgcggccgcggctacaacacgcac
cagtacaccaaggtgtggcagtgcaactgcaagttccactggtgctgcttcgtcaagtgc
aacacctgcagcgagcgcaccgaggtctacacctgcaagtga

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