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This gene belongs to the cytidylyltransferase family and is involved in the regulation of phosphatidylcholine biosynthesis. Mutations in this gene are associated with spondylometaphyseal dysplasia with cone-rod dystrophy. Alternatively spliced transcript variants have been found for this gene.
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Protein Aliases: CCT A; CCT-alpha; choline phosphate cytidylyltransferase 1 alpha; Choline-phosphate cytidylyltransferase A; CT A; CTP phosphocholine cytidylyl transferase; CTP:phosphocholine cytidylyl transferase; CTP:phosphocholine cytidylyltransferase A; CTP:phosphocholine cytidylyltransferase alpha; phosphate cytidylyltransferase 1, choline, alpha isoform; Phosphorylcholine transferase A
Gene Aliases: CCT-alpha; CCTA; Cctalpha; CT; CTA; CTalpha; CTP; CTPCT; Cttalpha; PCYT1; PCYT1A; SMDCRD
UniProt ID: (Human) P49585, (Mouse) P49586, (Rat) P19836
Entrez Gene ID: (Human) 5130, (Mouse) 13026, (Rat) 140544
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