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Intellectual disability update Jan 2018

Gene: LRAT

Red List (low evidence)
LRAT (lecithin retinol acyltransferase)
EnsemblGeneIds (GRCh38): ENSG00000121207
EnsemblGeneIds (GRCh37): ENSG00000121207
OMIM: 604863, Gene2Phenotype
LRAT is in 11 panels

1 review

Eleanor Williams (Genomics England Curator)

Comment on list classification: Associated with Leber congenital amaurosis 14 (MIM:613341), Retinal dystrophy, early-onset severe (MIM:613341), Retinitis pigmentosa, juvenile (MIM:613341) in OMIM and LEBER CONGENITAL AMAUROSIS in Gene2Phenotype. No evidence of association with intellectual disability from these two sources or PubMed searches.
Created: 8 Mar 2018, 1:41 p.m.
Created: 8 Mar 2018, 1:26 p.m.

Panel version: 0.439

History Filter Activity

8 Mar 2018, Gel status: 1

Gene classified by Genomics England curator

Eleanor Williams (Genomics England Curator)

This gene has been classified as Red List (Low Evidence).

18 Dec 2017, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

LRAT was added to Intellectual disability update Jan 2018 panel. Sources: Expert Review Red

18 Dec 2017, Gel status: 1

Created

Ellen McDonagh (Genomics England Curator)

LRAT was created by Ellen McDonagh