HGNC:10272
Homo sapiens
False
genetic disease, nuclear mRNA splicing via spliceosome, snRNP, U4_U6 snRNP
GO:0000398
nuclear mRNA splicing, via spliceosome
GO:0003734
small nuclear ribonucleoprotein
missense mutations in autosomal dominant RP
PRP3
Saccharomyces cerevisiae