Homo sapiens Wnt family member 10A (WNT10A), RefSeqGene on chromosome - Nucleotide

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Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia. [BMC Oral Health. 2024]
Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.
Liu Y, Sun J, Zhang C, Wu Y, Ma S, Li X, Wu X, Gao Q. BMC Oral Health. 2024 Jan 27; 24(1):136. Epub 2024 Jan 27.
SENP3 Promotes Mantle Cell Lymphoma Development through Regulating Wnt10a Expression. [Curr Med Sci. 2024]
SENP3 Promotes Mantle Cell Lymphoma Development through Regulating Wnt10a Expression.
Ma YN, Zou YD, Liu ZL, Wu GX, Zhou YZ, Luo CX, Huang XT, Xie ML, Xu SN, Li X. Curr Med Sci. 2024 Feb; 44(1):134-143. Epub 2024 Jan 25.
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss. [Br J Dermatol. 2023]
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss.
Cesarato N, Schwieger-Briel A, Gossmann Y, Henne SK, Hillmann K, Frommherz LH, Wehner M, Xiong X, Thiele H, Oji V, et al. Br J Dermatol. 2023 Nov 16; 189(6):741-749.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the WNT10A gene.

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Nucleotide