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LRAT

lecithin retinol acyltransferase

HCNC Approved Symbol
LRAT (HGNC:6685)
Genomic Coordinates
4:154,740,838 - 154,753,120 (4q32.1)
Synonyms
LCA14
Disease Associations
This gene is associated with the following 3 diseases in OMIM.

Diagnosed Cases

2Patients

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

Frequently observed phenotypes

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

Retinal dystrophy
 2 (100.0%)
LRAT - Gene browser | 3billion