LOVD - Variant listings for RPS19

About this overview [Show]

Patient data (#0000048)
Patient ID pat1rps1900016
Gender m
Malformations None
Growth Retardation no
Steroid Response na
Complications -
Variant Origin sporadic?(parents not tested)
Reference Ramenghi et al (2000) Blood Cells Mol Dis 26, 417-22
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 02
DNA change c.53T>C   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Leu18Pro
Frequency -
DB-ID RPS19_00016
Location -
Remarks Missense mutation
Molecula Mechanisms transition
Functional_Classific Reduces RPS19 protein levels and impairs nucleolar localization
mRNA_Expression -
Protein_Expression Reduced protein levels. Protein instability (in HEK293 cells) [1]
Protein_Localization No nucleolar localization, no ribosome association(in Hela and HEK293 cells) [1]
rRNA_Metabolism -
Protein_Synthesis -
Cell_Growth -
Functional_Remarks -
Functional_Reference [1] Angelini et al (2007) Hum Mol Genet 16, 1720-7

1 entry in RPS19

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
RNA change Descending
Ascending
Protein Descending
Ascending
Frequency Descending
Ascending
DB-ID Descending
Ascending
Location Descending
Ascending
Remarks Descending
Ascending
Molecula Mechanisms Descending
Ascending
Functional_Classific Descending
Ascending
mRNA_Expression Descending
Ascending
Protein_Expression Descending
Ascending
Protein_Localization Descending
Ascending
rRNA_Metabolism Descending
Ascending
Protein_Synthesis Descending
Ascending
Cell_Growth Descending
Ascending
Functional_Remarks Descending
Ascending
Functional_Reference Descending
Ascending
+/+ Unknown 02 c.53T>C - p.Leu18Pro - RPS19_00016 - Missense mutation transition Reduces RPS19 protein levels and impairs nucleolar localization - Reduced protein levels. Protein instability (in HEK293 cells) [1] No nucleolar localization, no ribosome association(in Hela and HEK293 cells) [1] - - - - [1] Angelini et al (2007) Hum Mol Genet 16, 1720-7