KEGG   Pan paniscus (bonobo): 100992168
Entry
100992168         CDS       T02283                                 
Symbol
WNT4
Name
(RefSeq) protein Wnt-4 isoform X1
  KO
K00408  wingless-type MMTV integration site family, member 4
Organism
pps  Pan paniscus (bonobo)
Pathway
pps04150  mTOR signaling pathway
pps04310  Wnt signaling pathway
pps04360  Axon guidance
pps04390  Hippo signaling pathway
pps04550  Signaling pathways regulating pluripotency of stem cells
pps04916  Melanogenesis
pps04919  Thyroid hormone signaling pathway
pps04934  Cushing syndrome
pps05010  Alzheimer disease
pps05022  Pathways of neurodegeneration - multiple diseases
pps05165  Human papillomavirus infection
pps05200  Pathways in cancer
pps05205  Proteoglycans in cancer
pps05217  Basal cell carcinoma
pps05224  Breast cancer
pps05225  Hepatocellular carcinoma
pps05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pps00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100992168 (WNT4)
   04390 Hippo signaling pathway
    100992168 (WNT4)
   04150 mTOR signaling pathway
    100992168 (WNT4)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100992168 (WNT4)
 09150 Organismal Systems
  09152 Endocrine system
   04919 Thyroid hormone signaling pathway
    100992168 (WNT4)
   04916 Melanogenesis
    100992168 (WNT4)
  09158 Development and regeneration
   04360 Axon guidance
    100992168 (WNT4)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100992168 (WNT4)
   05205 Proteoglycans in cancer
    100992168 (WNT4)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100992168 (WNT4)
   05226 Gastric cancer
    100992168 (WNT4)
   05217 Basal cell carcinoma
    100992168 (WNT4)
   05224 Breast cancer
    100992168 (WNT4)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100992168 (WNT4)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100992168 (WNT4)
   05022 Pathways of neurodegeneration - multiple diseases
    100992168 (WNT4)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100992168 (WNT4)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pps00536]
    100992168 (WNT4)
Glycosaminoglycan binding proteins [BR:pps00536]
 Heparan sulfate / Heparin
  Morphogens
   100992168 (WNT4)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100992168
NCBI-ProteinID: XP_034813661
Ensembl: ENSPPAG00000009237
Position
1:complement(21310228..21335985)
AA seq 351 aa
MSPRSCLRSLRLLVFAVFSAAASNWLYLAKLSSVGSISEEETCEKLKGLIQRQVQMCKRN
LEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAISSAGV
AFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRERSKGAS
SSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALKEKFDG
ATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGTRGRTCNKTS
KAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR
NT seq 1056 nt   +upstreamnt  +downstreamnt
atgagtccccgctcgtgcctgcgttcgctgcgcctcctcgtcttcgccgtcttctcagcc
gccgcgagcaactggctgtacctggccaagctgtcgtcggtggggagcatctcagaggag
gagacgtgcgagaaactcaagggcctgatccagaggcaggtgcagatgtgcaagcggaac
ctggaagtcatggactcggtgcgccgcggtgcccagctggccattgaggagtgccagtac
cagttccggaaccggcgctggaactgctccacactcgactccttgcccgtcttcggcaag
gtggtgacgcaagggactcgggaggcggccttcgtgtacgccatctcttcggcaggtgtg
gcctttgcagtgacgcgggcgtgcagcagtggggagctggagaagtgcggctgtgacagg
acggtgcatggggtcagtccacagggcttccagtggtcaggatgctctgacaacatcgcc
tacggtgtggccttctcacagtcgtttgtggatgtgcgggagagaagcaagggggcctca
tccagcagagccctcatgaacctccacaacaatgaggccggcaggaaggccatcctgaca
cacatgcgggtggaatgcaagtgccacggggtgtcaggctcctgtgaggtaaagacgtgc
tggcgagccgtgccgcccttccgccaggtgggtcacgcactgaaggagaagtttgatggt
gccactgaggtggagccacgccgcgtgggctcctccagggcactggtgccacgcaacgca
cagttcaagccgcacacagatgaggacctggtgtacttggagcctagccccgacttctgt
gagcaggacatgcgcagcggcgtgctgggcacgaggggccgcacatgcaacaagacgtcc
aaggccatcgacggctgtgagctgctgtgctgtggccgcggcttccacacggcgcaggtg
gagctggctgaacgctgcagctgcaaattccactggtgctgcttcgtcaagtgccggcag
tgccagcggctcgtggagttgcacacgtgccgatga

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