chromosome 16 open reading frame 33, isoform CRA_b [Homo sapiens]

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Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma. [J Hematol Oncol. 2014]
Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma.
Yang J, Annala M, Ji P, Wang G, Zheng H, Codgell D, Du X, Fang Z, Sun B, Nykter M, et al. J Hematol Oncol. 2014 Oct 10; 7:76. Epub 2014 Oct 10.
A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter. [Science. 2006]
A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter.
De Gobbi M, Viprakasit V, Hughes JR, Fisher C, Buckle VJ, Ayyub H, Gibbons RJ, Vernimmen D, Yoshinaga Y, de Jong P, et al. Science. 2006 May 26; 312(5777):1215-7.
Minor spliceosome components are predominantly localized in the nucleus. [Proc Natl Acad Sci U S A. 2008]
Minor spliceosome components are predominantly localized in the nucleus.
Pessa HK, Will CL, Meng X, Schneider C, Watkins NJ, Perälä N, Nymark M, Turunen JJ, Lührmann R, Frilander MJ. Proc Natl Acad Sci U S A. 2008 Jun 24; 105(25):8655-60. Epub 2008 Jun 16.

RefSeq genomic sequence
See the genomic reference sequence for the SNRNP25 gene (NG_017004.2).
RefSeq protein
See the reference protein sequence for U11/U12 small nuclear ribonucleoprotein 25 kDa protein (NP_078847.2).

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Protein