TMX3

thioredoxin related transmembrane protein 3
OMIM: 616102, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber TMX3 in Structural eye disease Version 3.77 Latest signed off version: v3.0 (22 Mar 2023)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber NHS GMS Phenotypes Microphthalmia, coloboma, micrognathia, diaphragmatic hernia None

Panel

Reviews

Mode of inheritance

Details

Version 3.77
Latest signed off version: v3.0 (22 Mar 2023)

review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted