KEGG   Phyllostomus discolor (pale spear-nosed bat): 114513331
Entry
114513331         CDS       T07739                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
pdic  Phyllostomus discolor (pale spear-nosed bat)
Pathway
pdic04150  mTOR signaling pathway
pdic04310  Wnt signaling pathway
pdic04390  Hippo signaling pathway
pdic04550  Signaling pathways regulating pluripotency of stem cells
pdic04916  Melanogenesis
pdic04934  Cushing syndrome
pdic05010  Alzheimer disease
pdic05022  Pathways of neurodegeneration - multiple diseases
pdic05165  Human papillomavirus infection
pdic05200  Pathways in cancer
pdic05205  Proteoglycans in cancer
pdic05217  Basal cell carcinoma
pdic05224  Breast cancer
pdic05225  Hepatocellular carcinoma
pdic05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pdic00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    114513331 (WNT7B)
   04390 Hippo signaling pathway
    114513331 (WNT7B)
   04150 mTOR signaling pathway
    114513331 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    114513331 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    114513331 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    114513331 (WNT7B)
   05205 Proteoglycans in cancer
    114513331 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    114513331 (WNT7B)
   05226 Gastric cancer
    114513331 (WNT7B)
   05217 Basal cell carcinoma
    114513331 (WNT7B)
   05224 Breast cancer
    114513331 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    114513331 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    114513331 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    114513331 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    114513331 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pdic00536]
    114513331 (WNT7B)
Glycosaminoglycan binding proteins [BR:pdic00536]
 Heparan sulfate / Heparin
  Morphogens
   114513331 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 114513331
NCBI-ProteinID: XP_028388421
UniProt: A0A6J2N911
LinkDB
Position
2:complement(215115889..215159670)
AA seq 353 aa
MLLLSPRGALLSLYCPQIFLILSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP
DAIIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA
HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA
RRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV
QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR
TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1062 nt   +upstreamnt  +downstreamnt
atgctcctgctgtcgccgcgcggcgcgctgctctccctctattgcccgcagatctttctc
atcttgtccagcggcagctacctagcgctgtcctcggtcgtggccctgggagccaacatc
atctgcaacaagatccccggtctggccccgcggcagcgcgccatctgccagagccggccc
gacgccatcatcgtgatcggcgagggtgcgcagatgggcatcaacgagtgccagtaccag
ttccgcttcgggcgctggaactgctccgcgctcggcgagaagacggtcttcgggcaggag
ctccgagtagggagccgtgaggccgccttcacgtacgccatcaccgcagcgggcgtggcc
cacgcggtcaccgccgcctgcagccagggcaacctgagcaactgcggctgcgaccgcgag
aagcagggctactacaaccaggccgagggctggaagtggggcggctgctcggccgacgtg
cgctacggcatcgacttctcccggcgcttcgtggacgcgcgcgagatcaagaagaacgcg
cgtcgcctcatgaacctgcacaacaacgaggcaggcaggaaggtcctggaggagcgcatg
aagctggagtgcaagtgccacggggtgtcgggctcctgcaccaccaagacctgctggacc
acgctgcccaagttccgcgaggtgggccacctgctcaaggagaagtacaacgcggccgtg
caggtggaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaagcag
ctgcgcagctaccagaagcccatggagacggacctggtgtacatcgagaagtcgcccaac
tactgcgaggaggacgcggccacgggcagcgtgggcacgcagggccgcctgtgcaaccgc
acgtcgcccggcgcggacggctgcgacaccatgtgctgcggccgcggctacaacacgcac
cagtacaccaaggtctggcagtgcaactgcaagttccactggtgctgcttcgtcaagtgc
aacacctgcagcgagcgcaccgaggtcttcacctgcaagtga

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