Piliocolobus tephrosceles (Ugandan red Colobus): 111547777
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Entry
111547777 CDS
T07491
Symbol
WNT4
Name
(RefSeq) protein Wnt-4
KO
K00408
wingless-type MMTV integration site family, member 4
Organism
pteh
Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh04150
mTOR signaling pathway
pteh04310
Wnt signaling pathway
pteh04360
Axon guidance
pteh04390
Hippo signaling pathway
pteh04519
Cadherin signaling
pteh04550
Signaling pathways regulating pluripotency of stem cells
pteh04916
Melanogenesis
pteh04919
Thyroid hormone signaling pathway
pteh04934
Cushing syndrome
pteh05010
Alzheimer disease
pteh05022
Pathways of neurodegeneration - multiple diseases
pteh05165
Human papillomavirus infection
pteh05200
Pathways in cancer
pteh05205
Proteoglycans in cancer
pteh05217
Basal cell carcinoma
pteh05224
Breast cancer
pteh05225
Hepatocellular carcinoma
pteh05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pteh00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
111547777 (WNT4)
04390 Hippo signaling pathway
111547777 (WNT4)
04150 mTOR signaling pathway
111547777 (WNT4)
09133 Signaling molecules and interaction
04519 Cadherin signaling
111547777 (WNT4)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
111547777 (WNT4)
09150 Organismal Systems
09152 Endocrine system
04919 Thyroid hormone signaling pathway
111547777 (WNT4)
04916 Melanogenesis
111547777 (WNT4)
09158 Development and regeneration
04360 Axon guidance
111547777 (WNT4)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
111547777 (WNT4)
05205 Proteoglycans in cancer
111547777 (WNT4)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
111547777 (WNT4)
05226 Gastric cancer
111547777 (WNT4)
05217 Basal cell carcinoma
111547777 (WNT4)
05224 Breast cancer
111547777 (WNT4)
09172 Infectious disease: viral
05165 Human papillomavirus infection
111547777 (WNT4)
09164 Neurodegenerative disease
05010 Alzheimer disease
111547777 (WNT4)
05022 Pathways of neurodegeneration - multiple diseases
111547777 (WNT4)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
111547777 (WNT4)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pteh00536
]
111547777 (WNT4)
Glycosaminoglycan binding proteins [BR:
pteh00536
]
Heparan sulfate / Heparin
Morphogens
111547777 (WNT4)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
111547777
NCBI-ProteinID:
XP_023075630
Ensembl:
ENSPTEG00000010295
LinkDB
All DBs
Position
1:200578387..200604528
Genome browser
AA seq
296 aa
AA seq
DB search
MCKRNLEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAI
SSAGVAFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRER
SKGASSSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALK
EKFDGATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGTRGRT
CNKTSKAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR
NT seq
891 nt
NT seq
+upstream
nt +downstream
nt
atgtgcaagaggaacctggaagtcatggactcggtgcgtcgcggtgcccaactggccatt
gaggagtgccagtaccagttccggaaccggcgctggaactgctccacgctcgactccctg
cccgtcttcggcaaggtggtgacgcaagggactcgggaggcggccttcgtgtacgccatc
tcttcggcaggtgtggcctttgcagtgacgcgggcgtgcagcagtggggagctggagaag
tgtggctgtgaccggacggtgcacggggtcagcccacagggcttccagtggtcaggatgc
tctgacaacatcgcctacggtgtggccttctcacagtcgtttgtggatgtgcgggagaga
agtaagggggcctcgtccagcagagctctcatgaacctccacaacaatgaggccggcagg
aaggccatcctgacacacatgcgggtggaatgcaagtgccacggggtgtcaggctcctgt
gaggtaaagacgtgctggcgagccgtgccgcccttccgccaggtgggtcacgcactgaag
gagaagtttgatggtgccactgaagtggagccacgccgtgtgggctcctccagggcactg
gtgccacgcaatgcacagttcaagccgcacacagatgaggacctggtgtacttggagccc
agccctgacttctgcgagcaggacatgcgcagcggcgtgctgggcacaaggggccgcaca
tgcaacaagacgtccaaggccatcgacggctgtgagctgctgtgctgtggccgcggcttc
cacacggcgcaggtggagctggctgaacgctgcagctgcaaattccactggtgctgcttc
gtcaagtgccggcagtgccagcggctcgtggagttgcacacgtgccgatga
DBGET
integrated database retrieval system
