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Analysis of cDNA clones indicates that ribosome binding protein 1 may exist in different forms due to removal of tandem repeats, or partial intraexonic splicing of RRBP1. The form presented here is lacking the canine p180 ribosome-binding domain, NQGKKAEGAQ, which is tandemly repeated close to the N-terminus in other forms that haven't been fully characterized. RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome. Alternate splicing results in multiple transcript variants.
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Protein Aliases: 180 kDa ribosome receptor homolog; ES/130-related protein; mRRp; ribosome binding protein 1 homolog 180kDa (dog); Ribosome receptor protein; Ribosome-binding protein 1; RP11-462D18.3; RRp
Gene Aliases: 1700087N07Rik; 5730465C04Rik; ES/130; ES130; hES; KIAA1398; mKIAA1398; mRRp0; mRRp1.8; mRRp10; mRRp15a; mRRp15b; mRRp16.8; mRRp2; mRRp41; mRRp47; mRRp5.4; p180; RRBP1; RRp
UniProt ID: (Human) Q9P2E9, (Mouse) Q99PL5
Entrez Gene ID: (Human) 6238, (Mouse) 81910
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