Homo sapiens (human): 54361
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Entry
54361 CDS
T01001
Symbol
WNT4, SERKAL, WNT-4
Name
(RefSeq) Wnt family member 4
KO
K00408
wingless-type MMTV integration site family, member 4
Organism
hsa
Homo sapiens (human)
Pathway
hsa04150
mTOR signaling pathway
hsa04310
Wnt signaling pathway
hsa04360
Axon guidance
hsa04390
Hippo signaling pathway
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa04916
Melanogenesis
hsa04919
Thyroid hormone signaling pathway
hsa04934
Cushing syndrome
hsa05010
Alzheimer disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05165
Human papillomavirus infection
hsa05200
Pathways in cancer
hsa05205
Proteoglycans in cancer
hsa05217
Basal cell carcinoma
hsa05224
Breast cancer
hsa05225
Hepatocellular carcinoma
hsa05226
Gastric cancer
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06181
Salmonella
nt06215
WNT signaling (cancer)
nt06217
HH signaling (cancer)
nt06227
Nuclear receptor signaling (cancer)
nt06260
Colorectal cancer
nt06261
Gastric cancer
nt06263
Hepatocellular carcinoma
nt06269
Basal cell carcinoma
nt06270
Breast cancer
nt06271
Endometrial cancer
nt06274
Thyroid cancer
nt06505
WNT signaling
Element
N00010
Mutation-inactivated PTCH1 to Hedgehog signaling pathway
N00017
Mutation-activated SMO to Hedgehog signaling pathway
N00056
Wnt signaling pathway
N00059
FZD7-overexpression to Wnt signaling pathway
N00060
LRP6-overexpression to Wnt signaling pathway
N01362
Nuclear-initiated progesterone signaling pathway
N01442
Wnt signaling modulation, Wnt inhibitor
N01443
Wnt signaling modulation, Wnt acylation
Disease
H00600
Mullerian agenesis
H02317
SERKAL syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
54361 (WNT4)
04390 Hippo signaling pathway
54361 (WNT4)
04150 mTOR signaling pathway
54361 (WNT4)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
54361 (WNT4)
09150 Organismal Systems
09152 Endocrine system
04919 Thyroid hormone signaling pathway
54361 (WNT4)
04916 Melanogenesis
54361 (WNT4)
09158 Development and regeneration
04360 Axon guidance
54361 (WNT4)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
54361 (WNT4)
05205 Proteoglycans in cancer
54361 (WNT4)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
54361 (WNT4)
05226 Gastric cancer
54361 (WNT4)
05217 Basal cell carcinoma
54361 (WNT4)
05224 Breast cancer
54361 (WNT4)
09172 Infectious disease: viral
05165 Human papillomavirus infection
54361 (WNT4)
09164 Neurodegenerative disease
05010 Alzheimer disease
54361 (WNT4)
05022 Pathways of neurodegeneration - multiple diseases
54361 (WNT4)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
54361 (WNT4)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
hsa00536
]
54361 (WNT4)
Glycosaminoglycan binding proteins [BR:
hsa00536
]
Heparan sulfate / Heparin
Morphogens
54361 (WNT4)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
54361
NCBI-ProteinID:
NP_110388
OMIM:
603490
HGNC:
12783
Ensembl:
ENSG00000162552
UniProt:
P56705
LinkDB
All DBs
Position
1:complement(22117313..22143097)
Genome browser
AA seq
351 aa
AA seq
DB search
MSPRSCLRSLRLLVFAVFSAAASNWLYLAKLSSVGSISEEETCEKLKGLIQRQVQMCKRN
LEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAISSAGV
AFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRERSKGAS
SSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALKEKFDG
ATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGTRGRTCNKTS
KAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR
NT seq
1056 nt
NT seq
+upstream
nt +downstream
nt
atgagtccccgctcgtgcctgcgttcgctgcgcctcctcgtcttcgccgtcttctcagcc
gccgcgagcaactggctgtacctggccaagctgtcgtcggtggggagcatctcagaggag
gagacgtgcgagaaactcaagggcctgatccagaggcaggtgcagatgtgcaagcggaac
ctggaagtcatggactcggtgcgccgcggtgcccagctggccattgaggagtgccagtac
cagttccggaaccggcgctggaactgctccacactcgactccttgcccgtcttcggcaag
gtggtgacgcaagggactcgggaggcggccttcgtgtacgccatctcttcggcaggtgtg
gcctttgcagtgacgcgggcgtgcagcagtggggagctggagaagtgcggctgtgacagg
acagtgcatggggtcagcccacagggcttccagtggtcaggatgctctgacaacatcgcc
tacggtgtggccttctcacagtcgtttgtggatgtgcgggagagaagcaagggggcctcg
tccagcagagccctcatgaacctccacaacaatgaggccggcaggaaggccatcctgaca
cacatgcgggtggaatgcaagtgccacggggtgtcaggctcctgtgaggtaaagacgtgc
tggcgagccgtgccgcccttccgccaggtgggtcacgcactgaaggagaagtttgatggt
gccactgaggtggagccacgccgcgtgggctcctccagggcactggtgccacgcaacgca
cagttcaagccgcacacagatgaggacctggtgtacttggagcctagccccgacttctgt
gagcaggacatgcgcagcggcgtgctgggcacgaggggccgcacatgcaacaagacgtcc
aaggccatcgacggctgtgagctgctgtgctgtggccgcggcttccacacggcgcaggtg
gagctggctgaacgctgcagctgcaaattccactggtgctgcttcgtcaagtgccggcag
tgccagcggctcgtggagttgcacacgtgccgatga
DBGET
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