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LPCAT3 (Lysophosphatidylcholine Acyltransferase 3) is a Protein Coding gene. Diseases associated with LPCAT3 include Retinitis Pigmentosa 40 and Fanconi Anemia, Complementation Group D2. Among its related pathways are triacylglycerol biosynthesis and Glycerophospholipid biosynthesis. Gene Ontology (GO) annotations related to this gene include transferase activity, transferring acyl groups and 1-acylglycerophosphocholine O-acyltransferase activity. An important paralog of this gene is MBOAT1
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Protein Aliases: 1-acylglycerophosphocholine O-acyltransferase; 1-acylglycerophosphoethanolamine O-acyltransferase; 1-acylglycerophosphoserine O-acyltransferase; LPCAT; LPLAT 5; LPSAT; Lyso-PC acyltransferase 3; lyso-PS acyltransferase; Lysophosphatidylcholine acyltransferase; Lysophosphatidylcholine Acyltransferase 3; Lysophosphatidylserine acyltransferase; Lysophospholipid acyltransferase 5; membrane bound O-acyltransferase domain containing 5; Membrane-bound O-acyltransferase domain-containing protein 5; O-acyltransferase (membrane bound) domain containing 5; O-acyltransferase domain-containing protein 5; putative protein similar to nessy
Gene Aliases: C3F; LPCAT; LPCAT3; LPLAT 5; LPSAT; MBOAT5; nessy; OACT5
UniProt ID: (Human) Q6P1A2
Entrez Gene ID: (Human) 10162
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