Homo sapiens (human): 7481
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Entry
7481 CDS
T01001
Symbol
WNT11, HWNT11
Name
(RefSeq) Wnt family member 11
KO
K01384
wingless-type MMTV integration site family, member 11
Organism
hsa
Homo sapiens (human)
Pathway
hsa04150
mTOR signaling pathway
hsa04310
Wnt signaling pathway
hsa04390
Hippo signaling pathway
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa04916
Melanogenesis
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
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
7481 (WNT11)
04390 Hippo signaling pathway
7481 (WNT11)
04150 mTOR signaling pathway
7481 (WNT11)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
7481 (WNT11)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
7481 (WNT11)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
7481 (WNT11)
05205 Proteoglycans in cancer
7481 (WNT11)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
7481 (WNT11)
05226 Gastric cancer
7481 (WNT11)
05217 Basal cell carcinoma
7481 (WNT11)
05224 Breast cancer
7481 (WNT11)
09172 Infectious disease: viral
05165 Human papillomavirus infection
7481 (WNT11)
09164 Neurodegenerative disease
05010 Alzheimer disease
7481 (WNT11)
05022 Pathways of neurodegeneration - multiple diseases
7481 (WNT11)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
7481 (WNT11)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
hsa00536
]
7481 (WNT11)
Glycosaminoglycan binding proteins [BR:
hsa00536
]
Heparan sulfate / Heparin
Morphogens
7481 (WNT11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
7481
NCBI-ProteinID:
NP_004617
OMIM:
603699
HGNC:
12776
Ensembl:
ENSG00000085741
UniProt:
O96014
LinkDB
All DBs
Position
11:complement(76186325..76210761)
Genome browser
AA seq
354 aa
AA seq
DB search
MRARPQVCEALLFALALQTGVCYGIKWLALSKTPSALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTVVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELQDVAADLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq
1065 nt
NT seq
+upstream
nt +downstream
nt
atgagggcgcggccgcaggtctgcgaggcgctgctcttcgccctggcgctccagaccggc
gtgtgctatggcatcaagtggctggcgctgtccaagacaccatcggccctggcactgaac
cagacgcaacactgcaagcagctggagggtctggtgtctgcacaggtgcagctgtgccgc
agcaacctggagctcatgcacacggtggtgcacgccgcccgcgaggtcatgaaggcctgt
cgccgggcctttgccgacatgcgctggaactgctcctccattgagctcgcccccaactat
ttgcttgacctggagagagggacccgggagtcggccttcgtgtatgcgctgtcggccgcc
gccatcagccacgccatcgcccgggcctgcacctccggcgacctgcccggctgctcctgc
ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgcgcctctctggaaatgaagtgtaagtgccatggggtgtctggctcctgctccatc
cgcacctgctggaaggggctgcaggagctgcaggatgtggctgctgacctcaagacccga
tacctgtcggccaccaaggtagtgcaccgacccatgggcacccgcaagcacctggtgccc
aaggacctggatatccggcctgtgaaggactcggaactcgtctatctgcagagctcacct
gacttctgcatgaagaatgagaaggtgggctcccacgggacacaagacaggcagtgcaac
aagacatccaacggaagcgacagctgcgaccttatgtgctgcgggcgtggctacaacccc
tacacagaccgcgtggtcgagcggtgccactgtaagtaccactggtgctgctacgtcacc
tgccgcaggtgtgagcgtaccgtggagcgctatgtctgcaagtga
DBGET
integrated database retrieval system