Genomics England
GMS Panels
Panels
Genes and Entities

STX3

syntaxin 3
OMIM: 600876
PanelMode of inheritanceDetails
2 panels
Green
in Intestinal failure or congenital diarrhoea
R-numbers: R331
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microvillus inclusion disease, MONDO:0009635, diarrheal disorder, MONDO:0001673
Green
in Retinal disorders
R-numbers: R32
Signed-off version 7.8
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Retinal dystrophy and microvillus inclusion disease, OMIM:619446