Prionailurus bengalensis (leopard cat): 122480068
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Entry
122480068 CDS
T07574
Symbol
WNT4
Name
(RefSeq) protein Wnt-4 isoform X1
KO
K00408
wingless-type MMTV integration site family, member 4
Organism
pbg
Prionailurus bengalensis (leopard cat)
Pathway
pbg04150
mTOR signaling pathway
pbg04310
Wnt signaling pathway
pbg04360
Axon guidance
pbg04390
Hippo signaling pathway
pbg04519
Cadherin signaling
pbg04550
Signaling pathways regulating pluripotency of stem cells
pbg04916
Melanogenesis
pbg04919
Thyroid hormone signaling pathway
pbg04934
Cushing syndrome
pbg05010
Alzheimer disease
pbg05022
Pathways of neurodegeneration - multiple diseases
pbg05165
Human papillomavirus infection
pbg05200
Pathways in cancer
pbg05205
Proteoglycans in cancer
pbg05217
Basal cell carcinoma
pbg05224
Breast cancer
pbg05225
Hepatocellular carcinoma
pbg05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pbg00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
122480068 (WNT4)
04390 Hippo signaling pathway
122480068 (WNT4)
04150 mTOR signaling pathway
122480068 (WNT4)
09133 Signaling molecules and interaction
04519 Cadherin signaling
122480068 (WNT4)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
122480068 (WNT4)
09150 Organismal Systems
09152 Endocrine system
04919 Thyroid hormone signaling pathway
122480068 (WNT4)
04916 Melanogenesis
122480068 (WNT4)
09158 Development and regeneration
04360 Axon guidance
122480068 (WNT4)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
122480068 (WNT4)
05205 Proteoglycans in cancer
122480068 (WNT4)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
122480068 (WNT4)
05226 Gastric cancer
122480068 (WNT4)
05217 Basal cell carcinoma
122480068 (WNT4)
05224 Breast cancer
122480068 (WNT4)
09172 Infectious disease: viral
05165 Human papillomavirus infection
122480068 (WNT4)
09164 Neurodegenerative disease
05010 Alzheimer disease
122480068 (WNT4)
05022 Pathways of neurodegeneration - multiple diseases
122480068 (WNT4)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
122480068 (WNT4)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pbg00536
]
122480068 (WNT4)
Glycosaminoglycan binding proteins [BR:
pbg00536
]
Heparan sulfate / Heparin
Morphogens
122480068 (WNT4)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
122480068
NCBI-ProteinID:
XP_043429980
LinkDB
All DBs
Position
C1:complement(16215737..16244716)
Genome browser
AA seq
318 aa
AA seq
DB search
MSPRSCLRSLRLLVFAVFSAAASNWLYLAKLSSVGSISEEETCEKLKGLIQRQVQMCKRN
LEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAISSAGV
AFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRERSKGAS
SSRALMNLHNNEAGRKVGHALKEKFDGATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYL
EPSPDFCEQDVRSGVLGTRGRTCNKTSKAIDGCELLCCGRGFHTAQVELAERCSCKFHWC
CFVKCRQCQRLVELHTCR
NT seq
957 nt
NT seq
+upstream
nt +downstream
nt
atgagtccccgctcgtgcctgcgttcgctgcgcctcctggtcttcgctgtcttctcggcc
gccgcgagcaactggctgtacctggccaagctgtcctccgtggggagcatctcggaggag
gagacgtgcgagaagctcaagggcctgatccagaggcaggtgcagatgtgcaagcggaac
cttgaggtgatggactcggtgcgccgaggtgctcagctcgccatcgaggagtgccagtac
cagttccggaaccggcgctggaactgctccacgctcgactccctgcctgtcttcggcaag
gtggtgactcaagggacccgggaggcggccttcgtgtacgccatctcttcagcaggtgtg
gccttcgcggtgacgcgggcatgcagcagcggggagttggaaaagtgtggctgtgaccgg
acggtacatggagtcagcccgcagggcttccagtggtcgggatgctcggacaacatcgcc
tatggcgtggccttctcccagtccttcgtggacgtgcgggagagaagcaagggggcctca
tccagccgcgccctcatgaacctccacaacaacgaggctggcaggaaggtgggccacgca
ctcaaagagaagttcgacggcgccaccgaggtggagccacgccgcgtgggctcctccagg
gcgctggtgccgcgcaacgcacagttcaagccgcacacggatgaggacctggtgtatttg
gagcccagcccggacttctgcgagcaggacgtgcgcagcggcgtgctgggcacgaggggc
cgcacgtgcaacaagacgtccaaggccatcgacggctgcgagctgctgtgctgcggccgg
ggcttccacacggcccaggtggagctggccgagcgctgcagctgcaaattccactggtgc
tgcttcgtcaagtgccggcagtgccagcggctggtggagctgcacacgtgccggtga
DBGET
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