Peroxisomal disordersGene: TRIM37
Comment when marking as ready: Associated with phenotype in OMIM and G2P. At least seven variants reported patients from Finland, USA, Turkey and Czech Republic.
Created: 23 Aug 2016, 7:56 a.m.
Majority of patients are from the Finnish population. Not many reports in the literature.
Created: 23 Feb 2016, 2:57 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Promoted to V1 3rd October 2016
This gene has been classified as Green List (High Evidence).
Publications for TRIM37 were set to 17100991
TRIM37 was added to Peroxisomal disorderspanel. Sources: Emory Genetics Laboratory
Phenotypes for gene TRIM37 were set to Mulibrey nanism 253250
TRIM37 was created by sleigh
TRIM37 was added to Peroxisomal disorderspanel. Sources: Radboud University Medical Center, Nijmegen,Illumina TruGenome Clinical Sequencing Services