Gene Gene information from NCBI Gene database.
Entrez ID 7479
Gene name Wnt family member 8B
Gene symbol WNT8B
Synonyms (NCBI Gene)
-
Chromosome 10
Chromosome location 10q24.31
Summary 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.
54
miRTarBase ID miRNA Experiments Reference
MIRT025654 hsa-miR-7-5p Microarray 17612493
MIRT756277 hsa-miR-4757-3p Luciferase reporter assayWestern blottingqRT-PCR 36814555
MIRT1493988 hsa-miR-103a CLIP-seq
MIRT1493989 hsa-miR-107 CLIP-seq
MIRT1493990 hsa-miR-1179 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0005102 Function Signaling receptor binding IEA
GO:0005109 Function Frizzled binding IBA
GO:0005125 Function Cytokine activity IBA
GO:0005576 Component Extracellular region IEA
GO:0005576 Component Extracellular region TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601396 12789 ENSG00000075290
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q93098
Protein name Protein Wnt-8b
Protein function Ligand for members of the frizzled family of seven transmembrane receptors. May play an important role in the development and differentiation of certain forebrain structures, notably the hippocampus.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00110 wnt 34 334 wnt family Family
Tissue specificity TISSUE SPECIFICITY: Expression is restricted to the brain, and more specifically to the forebrain. {ECO:0000269|PubMed:9536085}.
Sequence
Sequence length 351
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
Disassembly of the destruction complex and recruitment of AXIN to the membrane
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs9420786 RCV005912044
Lung cancer Benign rs9420786 RCV005913028
Sarcoma Benign rs9420786 RCV005913027
Uterine corpus endometrial carcinoma Benign rs9420786 RCV005913029
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinogenesis Associate 33197287
Carcinoma Hepatocellular Associate 33197287
Endometrial Neoplasms Associate 38211843
Nasopharyngeal Carcinoma Associate 34287269
Neoplasm Metastasis Associate 34287269
Polycystic Ovary Syndrome Associate 29510649
Uterine Diseases Associate 29510649