KEGG   Gorilla gorilla gorilla (western lowland gorilla): 101139722
Entry
101139722         CDS       T02442                                 
Symbol
WNT4
Name
(RefSeq) protein Wnt-4 isoform X2
  KO
K00408  wingless-type MMTV integration site family, member 4
Organism
ggo  Gorilla gorilla gorilla (western lowland gorilla)
Pathway
ggo04150  mTOR signaling pathway
ggo04310  Wnt signaling pathway
ggo04360  Axon guidance
ggo04390  Hippo signaling pathway
ggo04550  Signaling pathways regulating pluripotency of stem cells
ggo04916  Melanogenesis
ggo04919  Thyroid hormone signaling pathway
ggo04934  Cushing syndrome
ggo05010  Alzheimer disease
ggo05022  Pathways of neurodegeneration - multiple diseases
ggo05165  Human papillomavirus infection
ggo05200  Pathways in cancer
ggo05205  Proteoglycans in cancer
ggo05217  Basal cell carcinoma
ggo05224  Breast cancer
ggo05225  Hepatocellular carcinoma
ggo05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ggo00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101139722 (WNT4)
   04390 Hippo signaling pathway
    101139722 (WNT4)
   04150 mTOR signaling pathway
    101139722 (WNT4)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101139722 (WNT4)
 09150 Organismal Systems
  09152 Endocrine system
   04919 Thyroid hormone signaling pathway
    101139722 (WNT4)
   04916 Melanogenesis
    101139722 (WNT4)
  09158 Development and regeneration
   04360 Axon guidance
    101139722 (WNT4)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101139722 (WNT4)
   05205 Proteoglycans in cancer
    101139722 (WNT4)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101139722 (WNT4)
   05226 Gastric cancer
    101139722 (WNT4)
   05217 Basal cell carcinoma
    101139722 (WNT4)
   05224 Breast cancer
    101139722 (WNT4)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101139722 (WNT4)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101139722 (WNT4)
   05022 Pathways of neurodegeneration - multiple diseases
    101139722 (WNT4)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101139722 (WNT4)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ggo00536]
    101139722 (WNT4)
Glycosaminoglycan binding proteins [BR:ggo00536]
 Heparan sulfate / Heparin
  Morphogens
   101139722 (WNT4)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 101139722
NCBI-ProteinID: XP_004024903
Ensembl: ENSGGOG00000022618
Position
1:complement(17973660..18001320)
AA seq 296 aa
MCKRNLEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAI
SSAGVAFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRER
SKGASSSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALK
EKFDGATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGTRGRT
CNKTSKAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR
NT seq 891 nt   +upstreamnt  +downstreamnt
atgtgcaagcggaacctggaagtcatggactcggtgcgccgcggtgcccaactggccatt
gaggagtgccagtaccagttccggaaccggcgctggaactgctccacactcgactccttg
cccgtcttcggcaaggtggtgacgcaagggactcgggaggcggccttcgtgtacgccatc
tcttcggcaggtgtggcctttgcagtgacgcgggcgtgcagcagtggggagctagagaag
tgcggctgtgacaggacggtgcatggggtcagcccacagggcttccagtggtcaggatgc
tctgacaacatcgcctacggcgtggccttctcacagtcgtttgtggatgtgcgggagaga
agcaagggggcctcgtccagcagagccctcatgaacctccacaacaatgaggccggcagg
aaggccatcctgacacacatgcgggtggaatgcaagtgccacggggtgtcaggctcctgt
gaggtaaagacgtgctggcgagccgtgccgcccttccgccaggtgggtcacgcactgaag
gagaagtttgatggtgccactgaggtggagccacgccgcgtgggctcctccagggcactg
gtgccacgcaacgcacagttcaagccgcacacagatgaggacctggtgtacttggagcct
agccccgacttctgtgagcaggacatgcgcagcggcgtgctgggcacgaggggccgcaca
tgcaacaagacgtccaaggccatcgacggctgtgagctgctgtgctgtggccgcggcttc
cacacggcgcaggtggagctggctgaacgctgcagctgcaaattccactggtgctgcttc
gtcaagtgccggcagtgccagcggctcgtggagttgcacacgtgccgatga

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