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MRPL9

Synonyms
L9mt
External resources
Summary
This is a nuclear gene encoding a protein component of the 39S subunit of the mitochondrial ribosome. Alternative splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 8.

Variant counts

The variants found in rare patients tested by 3billion are classified and counted according to ACMG guidelines. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc) are excluded.

Pathogenic
0
Likely pathogenic
0
VUS
13,944
Likely benign
398
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on MRPL9 gene.

Phenotype class
Patients in 3billion (%)

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