Camelus dromedarius (Arabian camel): 105088869
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Entry
105088869 CDS
T04642
Symbol
WNT4
Name
(RefSeq) protein Wnt-4
KO
K00408
wingless-type MMTV integration site family, member 4
Organism
cdk
Camelus dromedarius (Arabian camel)
Pathway
cdk04150
mTOR signaling pathway
cdk04310
Wnt signaling pathway
cdk04360
Axon guidance
cdk04390
Hippo signaling pathway
cdk04519
Cadherin signaling
cdk04550
Signaling pathways regulating pluripotency of stem cells
cdk04916
Melanogenesis
cdk04919
Thyroid hormone signaling pathway
cdk04934
Cushing syndrome
cdk05010
Alzheimer disease
cdk05022
Pathways of neurodegeneration - multiple diseases
cdk05165
Human papillomavirus infection
cdk05200
Pathways in cancer
cdk05205
Proteoglycans in cancer
cdk05217
Basal cell carcinoma
cdk05224
Breast cancer
cdk05225
Hepatocellular carcinoma
cdk05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
cdk00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
105088869 (WNT4)
04390 Hippo signaling pathway
105088869 (WNT4)
04150 mTOR signaling pathway
105088869 (WNT4)
09133 Signaling molecules and interaction
04519 Cadherin signaling
105088869 (WNT4)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
105088869 (WNT4)
09150 Organismal Systems
09152 Endocrine system
04919 Thyroid hormone signaling pathway
105088869 (WNT4)
04916 Melanogenesis
105088869 (WNT4)
09158 Development and regeneration
04360 Axon guidance
105088869 (WNT4)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
105088869 (WNT4)
05205 Proteoglycans in cancer
105088869 (WNT4)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
105088869 (WNT4)
05226 Gastric cancer
105088869 (WNT4)
05217 Basal cell carcinoma
105088869 (WNT4)
05224 Breast cancer
105088869 (WNT4)
09172 Infectious disease: viral
05165 Human papillomavirus infection
105088869 (WNT4)
09164 Neurodegenerative disease
05010 Alzheimer disease
105088869 (WNT4)
05022 Pathways of neurodegeneration - multiple diseases
105088869 (WNT4)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
105088869 (WNT4)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
cdk00536
]
105088869 (WNT4)
Glycosaminoglycan binding proteins [BR:
cdk00536
]
Heparan sulfate / Heparin
Morphogens
105088869 (WNT4)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
105088869
NCBI-ProteinID:
XP_031320165
LinkDB
All DBs
Position
13
Genome browser
AA seq
296 aa
AA seq
DB search
MCKRNLEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAI
SSAGVAFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRER
NKGASSSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALK
EKFDGATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGTRGRT
CNKTSKAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR
NT seq
891 nt
NT seq
+upstream
nt +downstream
nt
atgtgcaagcggaacctggaggtgatggactcggtgcgccgcggcgcccagctcgccatc
gaggagtgccagtaccagttccggaaccggcgctggaactgctccacgctcgactcgctg
cctgtctttggcaaggtggtgacgcaagggactcgggaggcggccttcgtgtacgccatc
tcttcggcaggtgtggccttcgcggtgacgcgggcatgcagcagcggggagcttgaaaag
tgcggctgtgaccggacggtacatggggtcagcccacagggcttccagtggtcaggatgc
tcggacaacattgcctacggtgtggccttctcacagtcgttcgtggacgtgcgggagaga
aacaagggggcctcgtccagccgggccctcatgaacctgcacaacaacgaggccggcagg
aaggctatcctgacacacatgcgggtggagtgcaagtgccacggggtgtcgggctcctgc
gaggtaaagacgtgctggcgagccgtgccgcccttccgccaggtgggccatgcactcaag
gagaagtttgatggagccaccgaggtggagccacgccgtgtgggctcctccagggcactg
gtgccgcgtaacgcgcagttcaagccacacacagatgaggacctggtgtacttggagccc
agcccagacttctgtgagcaggacatgcgcagcggcgtgctgggcacgaggggccgcacg
tgcaacaagacatccaaggccatcgacggctgtgagctgctgtgctgcggccgtggcttc
cacacagcacaggtagagctagctgagcgctgcagctgcaaattccactggtgctgcttc
gtcaagtgccggcagtgccagcgcctcgtcgagctgcacacgtgccggtga
DBGET
integrated database retrieval system