U4/U6 small nuclear ribonucleoprotein Prp31 isoform 2 [Mus musculus]

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Retinal Pigment Epithelial Cells: The Unveiled Component in the Etiology of Prpf Splicing Factor-Associated Retinitis Pigmentosa. [Adv Exp Med Biol. 2019]
Retinal Pigment Epithelial Cells: The Unveiled Component in the Etiology of Prpf Splicing Factor-Associated Retinitis Pigmentosa.
Hamieh A, Nandrot EF. Adv Exp Med Biol. 2019; 1185:227-231.
Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa. [Neurobiol Dis. 2007]
Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa.
Mordes D, Yuan L, Xu L, Kawada M, Molday RS, Wu JY. Neurobiol Dis. 2007 May; 26(2):291-300. Epub 2007 Mar 9.
Retinal pigment epithelium degeneration caused by aggregation of PRPF31 and the role of HSP70 family of proteins. [Mol Med. 2019]
Retinal pigment epithelium degeneration caused by aggregation of PRPF31 and the role of HSP70 family of proteins.
Valdés-Sánchez L, Calado SM, de la Cerda B, Aramburu A, García-Delgado AB, Massalini S, Montero-Sánchez A, Bhatia V, Rodríguez-Bocanegra E, Diez-Lloret A, et al. Mol Med. 2019 Dec 31; 26(1):1. Epub 2019 Dec 31.

RefSeq mRNA
See reference mRNA sequence for the Prpf31 gene (NM_001159714.1).
RefSeq protein isoforms
See the other reference sequence protein isoform for the Prpf31 gene (NP_081604.3).

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U4/U6 small nuclear ribonucleoprotein Prp31 isoform 2 [Mus musculus]
U4/U6 small nuclear ribonucleoprotein Prp31 isoform 2 [Mus musculus]
gi|228480238|ref|NP_001153186.1|

Protein
Mus musculus 10 days embryo whole body cDNA, RIKEN full-length enriched library,...
Mus musculus 10 days embryo whole body cDNA, RIKEN full-length enriched library, clone:2610209J23 product:glutathione reductase 1, full insert sequence
gi|12859251|dbj|AK019177.1|

Nucleotide

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Protein