Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7480
Gene name Gene Name - the full gene name approved by the HGNC.
Wnt family member 10B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WNT10B
Synonyms (NCBI Gene) Gene synonyms aliases
SHFM6, STHAG8, WNT-12
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q13.12
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
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs121918349 G>A,C,T Pathogenic Missense variant, coding sequence variant, synonymous variant, 3 prime UTR variant
rs763548858 ->TGCT Pathogenic Coding sequence variant, frameshift variant, intron variant
rs763991433 G>A,C Likely-pathogenic Coding sequence variant, stop gained, missense variant
rs766021478 C>T Pathogenic Coding sequence variant, stop gained, 3 prime UTR variant
rs776938956 TGT>- Pathogenic Inframe deletion, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018883 hsa-miR-335-5p Microarray 18185580
MIRT027804 hsa-miR-98-5p Microarray 19088304
MIRT053185 hsa-miR-148a-3p Luciferase reporter assay, Microarray, qRT-PCR, Western blot 22890324
MIRT463936 hsa-miR-376c-3p PAR-CLIP 23592263
MIRT463935 hsa-miR-545-5p PAR-CLIP 23592263
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000086 Process G2/M transition of mitotic cell cycle IEA
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0001649 Process Osteoblast differentiation IEA
GO:0002062 Process Chondrocyte differentiation IEP 15135146
GO:0005102 Function Signaling receptor binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601906 12775 ENSG00000169884
Protein
UniProt ID O00744
Protein name Protein Wnt-10b (Protein Wnt-12)
Protein function Member of the Wnt ligand gene family that encodes for secreted proteins, which activate the Wnt signaling cascade. Specifically activates canonical Wnt/beta-catenin signaling and thus triggers beta-catenin/LEF/TCF-mediated transcriptional progra
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00110 wnt 50 389 wnt family Family
Tissue specificity TISSUE SPECIFICITY: Detected in most adult tissues. Highest levels were found in heart and skeletal muscle. Low levels are found in brain.
Sequence
Sequence length 389
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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Split-Hand-Foot Malformation Split hand-foot malformation 6 rs763991433, rs1163162816, rs776938956, rs1592252556, rs121918349, rs763548858 N/A
Tooth Agenesis tooth agenesis, selective, 8 rs779326570, rs766021478 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Anodontia Associate 27321946, 31914153
Breast Neoplasms Associate 23372744, 35413424
Calcinosis Cutis Associate 29281678
Carcinogenesis Associate 19893992, 25995040
Carcinoma Hepatocellular Associate 19893992
Carcinoma Renal Cell Associate 33804101
Corneal endothelial dystrophy type 2 Associate 26370090
Deafness oligodontia syndrome Associate 27321946
Diastrophic dysplasia Associate 16942611
Dupuytren Contracture Associate 16942611