TSEN54 Chromosome 17

TRNA splicing endonuclease subunit 54
108 variants 108 Health Risk

Upload your DNA to see your personal genotypes for variants in TSEN54.

What This Gene Does
This gene encodes a subunit of the tRNA splicing endonuclease complex, which catalyzes the removal of introns from precursor tRNAs. The complex is also implicated in pre-mRNA 3-prime end processing. Mutations in this gene result in pontocerebellar hypoplasia type 2.[provided by RefSeq, Oct 2009]
Gene Info
Gene Group
tRNA-splicing endonuclease subunits
Locus Type
gene with protein product
Location
17q25.1
Ensembl
ENSG00000182173
Associated Conditions (30)
Inborn genetic diseases
Pontoneocerebellar hypoplasia
Pontocerebellar hypoplasia type 4
Pontocerebellar hypoplasia type 2A
Pontocerebellar hypoplasia type 5
Colorectal cancer
Thyroid cancer
nonmedullary
1
Gastric cancer
Malignant tumor of urinary bladder
Malignant tumor of esophagus
Familial cancer of breast
Olivopontocerebellar hypoplasia
TSEN54-related disorder
Abnormality of the nervous system
Microcephaly
Global developmental delay
Congenital cerebellar hypoplasia
Hypertonia
+10 more conditions
Key Variants
All Variants (108)
RSID Category Clinical Significance Conditions
RS113016401 Health Risk Conflicting classifications of pathogenicity
RS117456384 Health Risk Conflicting classifications of pathogenicity
RS1226320805 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1425806314 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS150805182 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS151332020 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS1555644694 Health Risk Conflicting classifications of pathogenicity
RS200015685 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Pontocerebellar hypoplasia type 4, Pontocerebellar hypoplasia type 2A
RS200228117 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 4, Pontocerebellar hypoplasia type 2A, Pontocerebellar hypoplasia type 5
RS200318170 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS200434678 Health Risk Conflicting classifications of pathogenicity Olivopontocerebellar hypoplasia, Pontoneocerebellar hypoplasia, Inborn genetic diseases
RS201089582 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia type 4, Pontocerebellar hypoplasia type 2A
RS201415896 Health Risk Conflicting classifications of pathogenicity
RS201948434 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Pontocerebellar hypoplasia type 2A, Pontocerebellar hypoplasia type 5
RS368377822 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS369805010 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, TSEN54-related disorder, Inborn genetic diseases
RS371709232 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373044979 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS377740590 Health Risk Conflicting classifications of pathogenicity
RS398124622 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 4, Pontocerebellar hypoplasia type 4
RS539437090 Health Risk Conflicting classifications of pathogenicity
RS577958629 Health Risk Conflicting classifications of pathogenicity
RS727504183 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS747473434 Health Risk Conflicting classifications of pathogenicity
RS751120868 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS754461779 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS756343304 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia type 4, Pontocerebellar hypoplasia type 2A
RS760089379 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Inborn genetic diseases, Pontoneocerebellar hypoplasia
RS762922379 Health Risk Conflicting classifications of pathogenicity
RS767631739 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS775864125 Health Risk Conflicting classifications of pathogenicity
RS776960594 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS779644096 Health Risk Conflicting classifications of pathogenicity
RS797046056 Health Risk Conflicting classifications of pathogenicity
RS886053396 Health Risk Conflicting classifications of pathogenicity Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS1024222577 Health Risk Likely pathogenic
RS1057517911 Health Risk Likely pathogenic
RS1598480419 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 2A, Pontocerebellar hypoplasia type 2A
RS2053367722 Health Risk Likely pathogenic
RS2053437943 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 5, Pontocerebellar hypoplasia type 5
RS2147006296 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 4, Pontocerebellar hypoplasia type 4
RS2147013931 Health Risk Likely pathogenic Abnormality of the nervous system, Abnormality of the nervous system
RS2147019791 Health Risk Likely pathogenic Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS2546150757 Health Risk Likely pathogenic
RS2546154115 Health Risk Likely pathogenic
RS2546156325 Health Risk Likely pathogenic Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS2546156411 Health Risk Likely pathogenic
RS2546158894 Health Risk Likely pathogenic
RS587784477 Health Risk Likely pathogenic Olivopontocerebellar hypoplasia, Olivopontocerebellar hypoplasia
RS765323986 Health Risk Likely pathogenic
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