KEGG   Trichosurus vulpecula (common brushtail): 118849996
Entry
118849996         CDS       T10126                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
tvp  Trichosurus vulpecula (common brushtail)
Pathway
tvp04150  mTOR signaling pathway
tvp04310  Wnt signaling pathway
tvp04390  Hippo signaling pathway
tvp04550  Signaling pathways regulating pluripotency of stem cells
tvp04916  Melanogenesis
tvp04934  Cushing syndrome
tvp05010  Alzheimer disease
tvp05022  Pathways of neurodegeneration - multiple diseases
tvp05165  Human papillomavirus infection
tvp05200  Pathways in cancer
tvp05205  Proteoglycans in cancer
tvp05217  Basal cell carcinoma
tvp05224  Breast cancer
tvp05225  Hepatocellular carcinoma
tvp05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:tvp00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    118849996 (WNT7B)
   04390 Hippo signaling pathway
    118849996 (WNT7B)
   04150 mTOR signaling pathway
    118849996 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    118849996 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    118849996 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    118849996 (WNT7B)
   05205 Proteoglycans in cancer
    118849996 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    118849996 (WNT7B)
   05226 Gastric cancer
    118849996 (WNT7B)
   05217 Basal cell carcinoma
    118849996 (WNT7B)
   05224 Breast cancer
    118849996 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    118849996 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    118849996 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    118849996 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    118849996 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:tvp00536]
    118849996 (WNT7B)
Glycosaminoglycan binding proteins [BR:tvp00536]
 Heparan sulfate / Heparin
  Morphogens
   118849996 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 118849996
NCBI-ProteinID: XP_036615043
LinkDB
Position
5:308892894..308986805
AA seq 353 aa
MLPACPHGALFSIYYPQIFLTLTSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQYQFRYGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQEEGWKWGGCSADVRYGIEFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEVVRASRLRQPTFLKVKQLRSYQKPLDTDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctccccgcctgcccgcacggcgctctcttctccatctactacccgcagatcttcctc
actcttaccagcggcagctacctagctctgtcatctgtggtggctttgggagccaatatc
atctgcaacaagatccctggcctggccccccgacaacgagccatctgtcagagccgcccc
gacgccatcatcgtgatcggagaaggtgcacagatggggatcaatgaatgccaataccag
ttccgctatggccgatggaactgttccgcactgggcgagaagactgtctttgggcaagag
ctgcgagtggggagccgggaagctgccttcacttacgccatcacagcagctggcgtggcc
catgcggtcactgcggcctgcagccaaggcaatttgagcaactgtggctgtgacagggag
aagcagggctactacaaccaggaggagggctggaagtggggcggctgctcggctgacgtc
cgctacggcatcgagttctccaggcgctttgtcgatgcccgtgagatcaagaagaatgcc
aggcggctgatgaacctgcataacaatgaagctggaagaaaggtcctcgaggaaaggatg
aagctagaatgcaaatgccacggagtgtcgggctcgtgcaccaccaagacgtgctggacc
acgctgcccaagttccgggaggtgggccacctgctcaaggagaagtacaacgcggcagtg
caggtagaggtggtgcgcgccagccgcctgcgccaacccaccttcctcaaggtcaagcag
ctacgcagctaccagaaacccctggacacggacctggtctacatcgagaagtcccctaac
tactgcgaggaggacgcggccacgggcagcgtgggcacccagggccgcctgtgcaaccgc
acgtcgcccggcgccgacggctgcgacaccatgtgctgcggccgcggctacaacacgcac
cagtacaccaaggtctggcagtgcaactgcaaattccactggtgctgcttcgtcaaatgc
aacacgtgcagcgagcggaccgaggtgttcacctgcaagtag

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