Gene: CA10

Alternate names for this Gene: CA-RPX|CARPX|HUCEP-15

Gene Summary: This gene encodes a protein that belongs to the carbonic anhydrase family of zinc metalloenzymes, which catalyze the reversible hydration of carbon dioxide in various biological processes. The protein encoded by this gene is an acatalytic member of the alpha-carbonic anhydrase subgroup, and it is thought to play a role in the central nervous system, especially in brain development. Multiple transcript variants encoding the same protein have been found for this gene.

Gene is located in Chromosome: 17

Location in Chromosome : 17q21.33-q22

Description of this Gene: carbonic anhydrase 10

Type of Gene: protein-coding

rs7215018 in CA10 gene and Adolescent idiopathic scoliosis PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs117399000 in CA10 gene and Blood Protein Measurement PMID 29875488 2018 Genomic atlas of the human plasma proteome.

PMID 30072576 2018 Co-regulatory networks of human serum proteins link genetics to disease.

rs9906298 in CA10 gene and Cholecystolithiasis PMID 17632509 2007 A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

rs9906298 in CA10 gene and Cholelithiasis PMID 17632509 2007 A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

rs756763 in CA10 gene and Hashimoto Disease PMID 30926877 2019 Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis.

rs8073930 in CA10 gene and Narcolepsy PMID 19629137 2009 Genome-wide association database developed in the Japanese Integrated Database Project.

rs7215018 in CA10 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2202237 in CA10 gene and Smoking PMID 30643258 2019 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.

rs756763 in CA10 gene and Thyroglobulin antibody measurement PMID 30926877 2019 Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis.