Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7481
Gene name Gene Name - the full gene name approved by the HGNC.
Wnt family member 11
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WNT11
Synonyms (NCBI Gene) Gene synonyms aliases
HWNT11
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.5
Summary Summary of gene provided in NCBI Entrez Gene.
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryog
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT707431 hsa-miR-5580-3p HITS-CLIP 21572407
MIRT707430 hsa-miR-5011-5p HITS-CLIP 21572407
MIRT707429 hsa-miR-190a-3p HITS-CLIP 21572407
MIRT707428 hsa-miR-6083 HITS-CLIP 21572407
MIRT736461 hsa-miR-504-3p Luciferase reporter assay, Western blotting, Immunohistochemistry (IHC), qRT-PCR, Flow cytometry 33142356
Transcription factors
Transcription factor Regulation Reference
ERG Activation 21242973
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001649 Process Osteoblast differentiation IEA
GO:0001837 Process Epithelial to mesenchymal transition IEA
GO:0003138 Process Primary heart field specification IEA
GO:0003139 Process Secondary heart field specification IEA
GO:0003151 Process Outflow tract morphogenesis IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603699 12776 ENSG00000085741
Protein
UniProt ID O96014
Protein name Protein Wnt-11
Protein function Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over only few cell diameter
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00110 wnt 47 354 wnt family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in fetal lung, kidney, adult heart, liver, skeletal muscle, and pancreas. {ECO:0000269|PubMed:11712081}.
Sequence
Sequence length 354
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  mTOR signaling pathway
Wnt signaling pathway
Hippo signaling pathway
Signaling pathways regulating pluripotency of stem cells
Melanogenesis
Cushing syndrome
Alzheimer disease
Pathways of neurodegeneration - multiple diseases
Human papillomavirus infection
Pathways in cancer
Proteoglycans in cancer
Basal cell carcinoma
Breast cancer
Hepatocellular carcinoma
Gastric cancer
  WNT ligand biogenesis and trafficking
Ca2+ pathway
PCP/CE pathway
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Congenital diaphragmatic hernia Congenital diaphragmatic hernia rs121908602, rs121908604, rs864309713, rs775394591 25783350
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Bone Diseases Metabolic Associate 34875064
Breast Neoplasms Associate 32635983, 34493366, 34911552
Carcinogenesis Associate 20103596, 27034261
Carcinoma Hepatocellular Inhibit 20103596
Carcinoma Non Small Cell Lung Associate 35692887
Carcinoma Pancreatic Ductal Associate 31718047
Carcinoma Squamous Cell Associate 23505429
Celiac Disease Associate 35208504
Chylomicronemia Familial due to Circulating Inhibitor of Lipoprotein Lipase Inhibit 29955137
Colorectal Neoplasms Associate 24504536, 37587207