Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
81029
Gene name Gene Name - the full gene name approved by the HGNC.
Wnt family member 5B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WNT5B
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12p13.33
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
MIRT022886 hsa-miR-124-3p Microarray 18668037
MIRT045371 hsa-miR-185-5p CLASH 23622248
MIRT1493833 hsa-miR-1275 CLIP-seq
MIRT1493834 hsa-miR-1324 CLIP-seq
MIRT1493835 hsa-miR-144 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002062 Process Chondrocyte differentiation IEP 15135146
GO:0005102 Function Signaling receptor binding IEA
GO:0005102 Function Signaling receptor binding IPI 19486338
GO:0005109 Function Frizzled binding IBA
GO:0005125 Function Cytokine activity IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606361 16265 ENSG00000111186
Protein
UniProt ID Q9H1J7
Protein name Protein Wnt-5b
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 50 359 wnt family Family
Sequence
Sequence length 359
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  mTOR signaling pathway
Wnt signaling pathway
Axon guidance
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
PCP/CE pathway
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Gout Gout N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Airway Remodeling Associate 27126693
Bone Diseases Associate 17900349
Breast Neoplasms Associate 29847788, 31462314
Carcinoma Hepatocellular Associate 19849855, 24944491
Carcinoma Non Small Cell Lung Associate 24980784
Carcinoma Renal Cell Associate 33804101
Cleft Palate Associate 25663376
Fibrosis Associate 24040439
Inflammation Associate 24040439
Inflammation Stimulate 27036869