Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 80326
MIM: 606268
HGNC: 13829
Ensembl: ENSG00000135925
Variants:
dbSNP: 80326
ClinVar: 80326
TCGA: ENSG00000135925
COSMIC: WNT10A
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000135925 | ENST00000258411 | Q9GZT5 |
| ENSG00000135925 | ENST00000258411 | A0A2K8FR47 |
| ENSG00000135925 | ENST00000458582 | H7BZB8 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38273178 | 2024 | SENP3 Promotes Mantle Cell Lymphoma Development through Regulating Wnt10a Expression. | 0 |
| 38280992 | 2024 | Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia. | 0 |
| 38273178 | 2024 | SENP3 Promotes Mantle Cell Lymphoma Development through Regulating Wnt10a Expression. | 0 |
| 38280992 | 2024 | Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia. | 0 |
| 35537890 | 2023 | Novel Dental Anomaly-associated Mutations in WNT10A Protein Binding Sites. | 4 |
| 37422997 | 2023 | Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia family. | 0 |
| 37566620 | 2023 | The investigation of WNT6 and WNT10A single nucleotide polymorphisms as potential biomarkers for dental pulp calcification in orthodontic patients. | 2 |
| 37671665 | 2023 | Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss. | 0 |
| 35537890 | 2023 | Novel Dental Anomaly-associated Mutations in WNT10A Protein Binding Sites. | 4 |
| 37422997 | 2023 | Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia family. | 0 |
| 37566620 | 2023 | The investigation of WNT6 and WNT10A single nucleotide polymorphisms as potential biomarkers for dental pulp calcification in orthodontic patients. | 2 |
| 37671665 | 2023 | Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss. | 0 |
| 35999385 | 2022 | WNT10A variants: following the pattern of inheritance in tooth agenesis and self-reported family history of cancer. | 2 |
| 35999385 | 2022 | WNT10A variants: following the pattern of inheritance in tooth agenesis and self-reported family history of cancer. | 2 |
| 33034246 | 2021 | Functional Effects of WNT10A Rare Variants Associated with Tooth Agenesis. | 13 |
Citation
Dessen P
WNT10A (Wnt family member 10A)
Atlas Genet Cytogenet Oncol Haematol. 2003-02-01
Online version: http://atlasgeneticsoncology.org/gene/42816/wnt10a-(wnt-family-member-10a)
