KEGG   Pipistrellus kuhlii (Kuhl's pipistrelle): 118708801
Entry
118708801         CDS       T07682                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
pkl  Pipistrellus kuhlii (Kuhl's pipistrelle)
Pathway
pkl04150  mTOR signaling pathway
pkl04310  Wnt signaling pathway
pkl04390  Hippo signaling pathway
pkl04550  Signaling pathways regulating pluripotency of stem cells
pkl04916  Melanogenesis
pkl04934  Cushing syndrome
pkl05010  Alzheimer disease
pkl05022  Pathways of neurodegeneration - multiple diseases
pkl05165  Human papillomavirus infection
pkl05200  Pathways in cancer
pkl05205  Proteoglycans in cancer
pkl05217  Basal cell carcinoma
pkl05224  Breast cancer
pkl05225  Hepatocellular carcinoma
pkl05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pkl00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    118708801 (WNT7B)
   04390 Hippo signaling pathway
    118708801 (WNT7B)
   04150 mTOR signaling pathway
    118708801 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    118708801 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    118708801 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    118708801 (WNT7B)
   05205 Proteoglycans in cancer
    118708801 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    118708801 (WNT7B)
   05226 Gastric cancer
    118708801 (WNT7B)
   05217 Basal cell carcinoma
    118708801 (WNT7B)
   05224 Breast cancer
    118708801 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    118708801 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    118708801 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    118708801 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    118708801 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pkl00536]
    118708801 (WNT7B)
Glycosaminoglycan binding proteins [BR:pkl00536]
 Heparan sulfate / Heparin
  Morphogens
   118708801 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 118708801
NCBI-ProteinID: XP_036276155
LinkDB
Position
Unknown
AA seq 356 aa
MAQPPAPDHAQKLPRVALLRVPLLRRPLREARSAVVRRGPRGQHHLQQDPRVGPAAARHL
PEPARCHHRDRGGGADGHQRVPVPVPLRPLELLRPRREDGLRAGAPRSREAAFTYAITAA
GVAHAVTAACSQGNLSNCGCDREKQGFYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIK
KNARRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYS
AAVQVEAVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRL
CNRTSPGADGCHTMCCGRGYNTHQYTRVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1071 nt   +upstreamnt  +downstreamnt
atggcgcagccccccgccccggatcatgcacagaaactcccgcgagtggctcttctacgt
gttcctctgcttcggcgtcctctacgtgaagctcggagcgctgtcgtccgtcgtggccct
cggggccaacatcatctgcaacaagatccccgggttggccccgcggcagcgcgccatctg
ccagagccggcccgatgccatcatcgtgatcggggagggggcgcagatgggcatcaacga
gtgccagtaccagttccgcttcggccgctggaactgctccgccctcggcgagaagacggt
cttcgggcaggagctccgaggagccgggaggccgccttcacctacgccatcacggcggcc
ggcgtggcgcacgccgtcacggccgcctgcagccagggcaacctgagcaactgcggctgc
gaccgcgagaagcagggcttctacaaccaggccgagggctggaagtggggcggctgctcg
gccgacgtgcgctacggcatcgacttctcccgccgcttcgtggacgcgcgcgagatcaag
aagaacgcgcggcgcctcatgaacctgcacaacaacgaggcgggccgcaaggtcctggag
gagcgcatgaagctggagtgcaagtgccacggcgtgtcgggctcctgcaccaccaagacc
tgctggaccacgctgcccaagttccgcgaggtgggccacctgctcaaggagaagtacagc
gcggctgtgcaggtggaggcggtgcgcgccagccggctgcggcagcccaccttcctgcgc
atcaagcagctgcgcagctaccagaagcccatggagacggacctggtgtacatcgagaag
tcgcccaactactgcgaggaggacgcggccacgggcagcgtgggcacacagggccggctg
tgcaaccgcacctcgcccggcgccgacggctgccacaccatgtgctgcggccgcggctac
aacacgcaccagtacacccgcgtgtggcagtgcaactgcaagttccactggtgctgcttc
gtcaagtgcaacacgtgcagcgagcgcaccgaggtcttcacctgcaagtga

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