Mar 30, 2025 · Complete information for CPT1A gene (Protein Coding), Carnitine Palmitoyltransferase 1A, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Mar 30, 2025 · This gene encodes a member of the carnitine/choline acetyltransferase family. The encoded protein regulates the beta-oxidation and transport of long-chain fatty acids into mitochondria, and may play a role in the regulation of feeding …

Mar 30, 2025 · Complete information for CPT1B gene (Protein Coding), Carnitine Palmitoyltransferase 1B, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Mar 30, 2025 · CPT2 (Carnitine Palmitoyltransferase 2) is a Protein Coding gene. Diseases associated with CPT2 include Carnitine Palmitoyltransferase Ii Deficiency, Infantile and Carnitine Palmitoyltransferase Ii Deficiency, Myopathic, Stress-Induced.

Mar 30, 2025 · CHPT1 (Choline Phosphotransferase 1) is a Protein Coding gene. Diseases associated with CHPT1 include Myasthenic Syndrome, Congenital, 20, Presynaptic and Peeling Skin Syndrome 2. Among its related pathways are Glycerophospholipid biosynthesis and One-carbon metabolism and related pathways.

Mar 28, 2025 · The protein encoded by this gene, basigin, is a plasma membrane protein that is important in spermatogenesis, embryo implantation, neural network formation, and tumor progression. Basigin is also a member of the immunoglobulin superfamily, ubiquitously expressed in various tissues.

Showing of 132 Results for cpt1 Search Time: 0 ms. Export Show: Symbol Description Category UniProt ID GIFtS GC id Score; 1: CPT1A: Carnitine Palmitoyltransferase 1A: Protein Coding: P50416: 61: GC11M068754: 15.78: 2: CPT2: Carnitine Palmitoyltransferase 2: Protein Coding ... Gene symbols for cpt1.

Mar 30, 2025 · CHKB-CPT1B (CHKB-CPT1B Readthrough (NMD Candidate)) is an RNA Gene, and is affiliated with the ncRNA class. Diseases associated with CHKB-CPT1B include Muscular Dystrophy, Congenital, Megaconial Type and Muscular Dystrophy. Gene Ontology (GO) annotations related to this gene include transferase activity, …

Mar 28, 2025 · ACACA (Acetyl-CoA Carboxylase Alpha) is a Protein Coding gene. Diseases associated with ACACA include Acetyl-Coa Carboxylase-Alpha Deficiency and Lipid Metabolism Disorder. Among its related pathways are Metabolism of water-soluble vitamins and cofactors and Metabolism of steroids.

Mar 30, 2025 · ACAT1 (Acetyl-CoA Acetyltransferase 1) is a Protein Coding gene. Diseases associated with ACAT1 include Alpha-Methylacetoacetic Aciduria and Disorder Of Keton Body Transport. Among its related pathways are Ketone body metabolism and Leucine, isoleucine and valine metabolism.