LOVD - Variant listings for RPS19

About this overview [Show]

Patient data (#0000165)
Patient ID pat1rps1900080
Gender f
Malformations Mental retardation
Growth Retardation na
Steroid Response na
Complications -
Variant Origin de novo, in patient
Reference Campagnoli et al (2004) Haematologica 89, 480-9
Template DNA
Technique Kar, STR
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 00
DNA change t(1;19)(p32;q13)
RNA change -
Protein p.0
Frequency -
DB-ID RPS19_00080
Location -
Remarks Translocation
Molecula Mechanisms -
Functional_Classific -
mRNA_Expression -
Protein_Expression -
Protein_Localization -
rRNA_Metabolism -
Protein_Synthesis -
Cell_Growth -
Functional_Remarks -
Functional_Reference -

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 00 t(1;19)(p32;q13) - p.0 - RPS19_00080 - Translocation - - - - - - - - - -