Gene: WNT10A

Alternate names for this Gene: OODD|SSPS|STHAG4

Gene Summary: 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 embryogenesis. This gene is a member of the WNT gene family. It is strongly expressed in the cell lines of promyelocytic leukemia and Burkitt's lymphoma. In addition, it and another family member, the WNT6 gene, are strongly coexpressed in colorectal cancer cell lines. The gene overexpression may play key roles in carcinogenesis through activation of the WNT-beta-catenin-TCF signaling pathway. This gene and the WNT6 gene are clustered in the chromosome 2q35 region.

Gene is located in Chromosome: 2

Location in Chromosome : 2q35

Description of this Gene: Wnt family member 10A

Type of Gene: protein-coding

Gene: LOC107984111

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

rs74333950 in WNT10A;LOC107984111 gene and Alopecia PMID 28196072 2017 Genetic prediction of male pattern baldness.

rs74333950 in WNT10A;LOC107984111 gene and Alopecia, Androgenetic, 1 PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

rs74333950 in WNT10A;LOC107984111 gene and Alopecia, Androgenetic, 2 PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

rs74333950 in WNT10A;LOC107984111 gene and Alopecia, Androgenetic, 3 PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

rs74333950 in WNT10A;LOC107984111 gene and Alopecia, Male Pattern PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

rs74333950 in WNT10A;LOC107984111 gene and Androgenetic Alopecia PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

rs121908119 in WNT10A;LOC107984111 gene and Dysmorphic features PMID 28105635 2017 Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.

PMID 24700731 2014 The WNT10A gene in ectodermal dysplasias and selective tooth agenesis.

PMID 24043634 2014 WNT10A variants are associated with non-syndromic tooth agenesis in the general population.

PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 25356970 2015 Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.

PMID 17847007 2007 Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.

rs121908119 in WNT10A;LOC107984111 gene and Muscle hypotonia PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 17847007 2007 Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.

PMID 25356970 2015 Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.

PMID 28105635 2017 Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.

PMID 24700731 2014 The WNT10A gene in ectodermal dysplasias and selective tooth agenesis.

PMID 24043634 2014 WNT10A variants are associated with non-syndromic tooth agenesis in the general population.

rs121908119 in WNT10A;LOC107984111 gene and Odontoonychodermal dysplasia PMID 25545742 2015 WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.

PMID 24398796 2014 Variability in dentofacial phenotypes in four families with WNT10A mutations.

PMID 25629078 2015 Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.

PMID 24902757 2014 Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

PMID 24702986 2014 Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review.

PMID 23167694 2013 Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

rs74333950 in WNT10A;LOC107984111 gene and Other alopecia PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

rs121908119 in WNT10A;LOC107984111 gene and SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) PMID 25629078 2015 Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.

PMID 24702986 2014 Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review.

PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 24398796 2014 Variability in dentofacial phenotypes in four families with WNT10A mutations.

PMID 24902757 2014 Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

PMID 23167694 2013 Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

rs121908119 in WNT10A;LOC107984111 gene and TOOTH AGENESIS, SELECTIVE, 4 (disorder) PMID 25545742 2015 WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.

PMID 24902757 2014 Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 24702986 2014 Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review.

PMID 24398796 2014 Variability in dentofacial phenotypes in four families with WNT10A mutations.

PMID 23167694 2013 Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

PMID 25629078 2015 Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.