AlphaFold predicted structure
WNT10A · Q9GZT5

Mean pLDDT
81.9/ 100
Confident
417 residues
Confidence breakdown
- Very high(≥ 90)52%
- Confident(70–90)24%
- Low(50–70)14%
- Very low(< 50)10%
AlphaFold (Jumper et al., 2021) · CC BY 4.0
Wnt family member 10A
Annotations refreshed 1 month ago.
Diagnostic Grade (Green)
Ectodermal dysplasia
BIALLELIC, autosomal or pseudoautosomalEctodermal dysplasia without a known gene mutation
BIALLELIC, autosomal or pseudoautosomalodonto-onycho-dermal dysplasia
tooth agenesis, selective, 4
Schöpf-Schulz-Passarge syndrome
tooth agenesis
ectodermal dysplasia WNT10A related
hereditary disease
dentures
androgenetic alopecia
Epidermal Inclusion Cyst
tooth agenesis, selective, 2
Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.
Protein Wnt-10a
Ligand for members of the frizzled family of seven transmembrane receptors (Probable). Functions in the canonical Wnt/beta-catenin signaling pathway (By similarity). Plays a role in normal ectoderm development (PubMed:17847007, PubMed:28589954). Required for normal tooth development (PubMed:17847007, PubMed:28589954, PubMed:29178643). Required for normal postnatal development and maintenance of tongue papillae and sweat ducts (PubMed:28589954). Required for normal proliferation of basal cells in tongue filiform papillae, plantar epithelium and sweat ducts. Required for normal expression of keratins in tongue papillae (By similarity). Required for normal expression of KRT9 in foot plant epithelium (PubMed:28589954). Required for normal hair follicle function (PubMed:28589954)
Curated MONDO disease pages that list WNT10A among their top associated genes.
WNT10A · Q9GZT5

Mean pLDDT
81.9/ 100
Confident
417 residues
Confidence breakdown
AlphaFold (Jumper et al., 2021) · CC BY 4.0