KEGG   Talpa occidentalis (Iberian mole): 119247151
Entry
119247151         CDS       T07495                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X2
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
tod  Talpa occidentalis (Iberian mole)
Pathway
tod04150  mTOR signaling pathway
tod04310  Wnt signaling pathway
tod04390  Hippo signaling pathway
tod04550  Signaling pathways regulating pluripotency of stem cells
tod04916  Melanogenesis
tod04934  Cushing syndrome
tod05010  Alzheimer disease
tod05022  Pathways of neurodegeneration - multiple diseases
tod05165  Human papillomavirus infection
tod05200  Pathways in cancer
tod05205  Proteoglycans in cancer
tod05217  Basal cell carcinoma
tod05224  Breast cancer
tod05225  Hepatocellular carcinoma
tod05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:tod00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    119247151 (WNT7B)
   04390 Hippo signaling pathway
    119247151 (WNT7B)
   04150 mTOR signaling pathway
    119247151 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    119247151 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    119247151 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    119247151 (WNT7B)
   05205 Proteoglycans in cancer
    119247151 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    119247151 (WNT7B)
   05226 Gastric cancer
    119247151 (WNT7B)
   05217 Basal cell carcinoma
    119247151 (WNT7B)
   05224 Breast cancer
    119247151 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    119247151 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    119247151 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    119247151 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    119247151 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:tod00536]
    119247151 (WNT7B)
Glycosaminoglycan binding proteins [BR:tod00536]
 Heparan sulfate / Heparin
  Morphogens
   119247151 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973 DUF7259
Other DBs
NCBI-GeneID: 119247151
NCBI-ProteinID: XP_037369275
LinkDB
Position
Unknown
AA seq 353 aa
MLLLSPRRALLSVYCPQLFLILSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEAVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctgctgtcgccgcgccgcgcgctgctctccgtctattgcccgcagctctttctc
atcctgtccagcggcagctacctagcgctgtcgtctgtcgtggccctgggagccaacatc
atctgcaataagatccccgggttggccccgcggcagcgcgccatctgccagagccggccc
gatgccatcatcgtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccag
ttccgcttcgggcgctggaactgctccgcgctgggcgagaagaccgtcttcgggcaggag
ctccgagtagggagccgcgaggccgccttcacctacgccatcaccgctgctggcgtggcc
cacgccgtcactgctgcctgcagccagggcaacctcagcaactgcgggtgcgaccgcgag
aagcagggctactacaaccaggccgagggctggaagtggggcggctgctcggccgacgtg
cgctacggcatcgacttctcccggcgcttcgtggacgcccgagagatcaagaagaacgcg
cggcgcctcatgaacctgcacaacaatgaggcgggcaggaaggtcctggaggagcgcatg
aagctggagtgcaagtgccacggcgtgtcgggctcctgcaccaccaagacgtgctggacc
acgctgcccaagttccgggaggtgggccacctgctcaaggagaagtacaacgcggccgtg
caggtggaggcggtgcgcgccagccgcctgcggcagcccaccttcctgcgcatcaagcag
ctgcgcagctaccagaagcccatggagacggacctggtgtacatcgagaagtcacccaac
tactgcgaggaggacgcggccacgggcagcgtgggcacgcagggccgcctgtgcaaccgc
acgtcgccgggcgccgacggctgcgacaccatgtgctgcggccgcggctacaacacccac
cagtacaccaaggtctggcagtgcaactgcaagttccactggtgctgcttcgtcaagtgc
aacacctgcagcgagcgcaccgaggtcttcacctgcaagtga

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