LARS2 - Gene browser

LARS2

leucyl-tRNA synthetase 2, mitochondrial

HCNC Approved Symbol: LARS2 (HGNC:17095)
Genomic Coordinates: 3:45,388,576 - 45,549,407 (3p21.31)
Synonyms: KIAA0028, LEURS, MGC26121, mtLeuRS
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

2Patients

In total, 2 patients were diagnosed with a variant in the LARS2 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

02
Patient count

Hearing loss: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Hypogonadism, hypogonadotropic: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Moyamoya phenomenon: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Neurofibromatosis: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
No secondary sexual characteristics at puberty: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)