Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51384
Gene name Gene Name - the full gene name approved by the HGNC.
Wnt family member 16
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WNT16
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q31.31
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
MIRT025130 hsa-miR-181a-5p Microarray 17612493
MIRT650766 hsa-miR-5584-5p HITS-CLIP 23824327
MIRT650765 hsa-miR-200a-5p HITS-CLIP 23824327
MIRT650764 hsa-miR-200b-5p HITS-CLIP 23824327
MIRT650763 hsa-miR-494-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003408 Process Optic cup formation involved in camera-type eye development ISS 16258938
GO:0005109 Function Frizzled binding IBA 21873635
GO:0005125 Function Cytokine activity IBA 21873635
GO:0005576 Component Extracellular region TAS
GO:0005615 Component Extracellular space IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606267 16267 ENSG00000002745
Protein
UniProt ID Q9UBV4
Protein name Protein Wnt-16
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 49 365 wnt family Family
Tissue specificity TISSUE SPECIFICITY: Isoform Wnt-16b is expressed in peripheral lymphoid organs such as spleen, appendix, and lymph nodes, in kidney but not in bone marrow. Isoform Wnt-16a is expressed at significant levels only in the pancreas.
Sequence
Sequence length 365
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
Transcriptional misregulation in cancer
Proteoglycans in cancer
Basal cell carcinoma
Breast cancer
Hepatocellular carcinoma
Gastric cancer
  WNT ligand biogenesis and trafficking
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Rheumatoid arthritis Rheumatoid Arthritis rs587776843 30251476
Unknown
Disease term Disease name Evidence References Source
Osteoporosis Osteoporosis GWAS
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Amyotrophic Lateral Sclerosis Associate 35355568
Beckwith Wiedemann Syndrome Associate 35507738
Bone Diseases Associate 34879876
Bone Diseases Metabolic Associate 37831088
Cardiovascular Diseases Associate 24243566
Cartilage Diseases Stimulate 36463522
Coffin Siris syndrome Associate 23300646
Colorectal Neoplasms Associate 37090726
Femoracetabular Impingement Stimulate 36463522
Fractures Bone Associate 32827035, 35689460