This ENU-induced T to A transversion in intron 3 disrupts a 5-prime splice donor sequence and has been shown to cause two novel splicing events in retinal pigment epithelium, one of which includes a portion of the intron downstream of exon 3 and is predicted to encode a short N-terminal polypeptide with 11 non-native amino acids and premature stop codon, and the other of which exon 3 is skipped leading to premature termination. (J:321062)
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cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count