Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7479
Gene name Gene Name - the full gene name approved by the HGNC.
Wnt family member 8B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WNT8B
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q24.31
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
MIRT025654 hsa-miR-7-5p Microarray 17612493
MIRT756277 hsa-miR-4757-3p Luciferase reporter assay, Western blotting, qRT-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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
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
GO:0007165 Process Signal transduction TAS 9536085
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601396 12789 ENSG00000075290
Protein
UniProt ID 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 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)
Associations from Text Mining
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