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Lrrk2 (leucine rich repeat kinase 2) is a protein coding gene Coli l10 ribosomal protein, belongs to the l10p family of ribosomal proteins. Diseases associated with lrrk2 include parkinson disease 8, autosomal dominant and parkinson's disease.
Function, proteins, disorders, pathways, orthologs, and expression. The protein, which is the functional equivalent of the e The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis.
This gene encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria
Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency. Mutations in this gene cause gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. Complete information for hnrnpu gene (protein coding), heterogeneous nuclear ribonucleoprotein u, including This gene is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin.
This gene encodes a ribosomal protein that is a component of the 60s subunit
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