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SCP2D1 (SCP2 Sterol Binding Domain Containing 1) is a Protein Coding gene. Diseases associated with SCP2D1 include Corneal Dystrophy, Posterior Polymorphous, 1 and D-Bifunctional Protein Deficiency. An important paralog of this gene is HSD17B4.
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Protein Aliases: likely ortholog of H. sapiens chromosome 20 open reading frame 79 (C20orf79); SCP2 sterol-binding domain containing 1; SCP2 sterol-binding domain-containing protein 1; sterol carrier protein 2-like protein
Gene Aliases: 1700010M22Rik; C20orf79; dJ1068E13.2; HSD22; RGD1308385; SCP2D1
UniProt ID: (Human) Q9UJQ7, (Mouse) Q9DAH1
Entrez Gene ID: (Human) 140856, (Rat) 311491, (Mouse) 66328
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