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This gene encodes one member of the sodium channel alpha subunit gene family Complete information for grin2a gene (protein coding), glutamate ionotropic receptor nmda type subunit 2a, including Allelic variants of this gene are associated with seizure disorders and autism spectrum disorder.
Lrrk2 (leucine rich repeat kinase 2) is a protein coding gene The cytochrome p450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. Diseases associated with lrrk2 include parkinson disease 8, autosomal dominant and parkinson's disease.
This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule.
The protein encoded by this gene is a major apoprotein of the chylomicron Function, proteins, disorders, pathways, orthologs, and expression. This gene encodes an enzyme that belongs to the family of dihydrodiol dehydrogenases, which exist in multiple forms in mammalian tissues and are involved in the metabolism of xenobiotics and sugars. The was gene product is a cytoplasmic protein, expressed exclusively in hematopoietic cells, which show signalling and cytoskeletal abnormalities in was patients.
This gene encodes a member of the cytochrome p450 superfamily of enzymes
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