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Intestinal failure or congenital diarrhoea v3.5 STX3 Achchuthan Shanmugasundram Phenotypes for gene: STX3 were changed from Microvillus inclusion disease, MONDO:0009635; diarrheal disorder, MONDO:0001673 to Diarrhea 12, with microvillus atrophy, OMIM:619445; Retinal dystrophy and microvillus inclusion disease, OMIM:619446
Intestinal failure or congenital diarrhoea v3.4 STX3 Achchuthan Shanmugasundram Publications for gene: STX3 were set to 24726755; 29266534; 25358429; 29282386
Intestinal failure or congenital diarrhoea v3.3 STX3 Achchuthan Shanmugasundram reviewed gene: STX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 33974130; Phenotypes: Diarrhea 12, with microvillus atrophy, OMIM:619445, Retinal dystrophy and microvillus inclusion disease, OMIM:619446; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intestinal failure or congenital diarrhoea v1.48 STX3 Eleanor Williams commented on gene: STX3
Intestinal failure or congenital diarrhoea v1.23 STX3 Ivone Leong Phenotypes for gene: STX3 were changed from Microvillus inclusion disease; congenital diarrheal disorder to Microvillus inclusion disease, MONDO:0009635; diarrheal disorder, MONDO:0001673
Intestinal failure or congenital diarrhoea v0.18 STX3 Ivone Leong Marked gene: STX3 as ready
Intestinal failure or congenital diarrhoea v0.18 STX3 Ivone Leong Added comment: Comment when marking as ready: As discussed in the GMS Gastrohepatology Specialist Test Group webex call 14th Jan 2019: The Specialist Test Group agreed that there is enough evidence to rate this gene green.
Intestinal failure or congenital diarrhoea v0.18 STX3 Ivone Leong Gene: stx3 has been classified as Green List (High Evidence).
Intestinal failure or congenital diarrhoea v0.18 STX3 Ivone Leong Publications for gene: STX3 were set to 24726755; 29266534; 25358429
Intestinal failure or congenital diarrhoea v0.17 STX3 Ivone Leong Mode of inheritance for gene: STX3 was changed from to BIALLELIC, autosomal or pseudoautosomal
Intestinal failure or congenital diarrhoea v0.16 STX3 Ivone Leong Phenotypes for gene: STX3 were changed from to Microvillus inclusion disease; congenital diarrheal disorder
Intestinal failure or congenital diarrhoea v0.15 STX3 Ivone Leong Publications for gene: STX3 were set to 24726755; 29266534
Intestinal failure or congenital diarrhoea v0.13 STX3 Ivone Leong Publications for gene: STX3 were set to
Intestinal failure or congenital diarrhoea v0.10 STX3 Miranda Durkie reviewed gene: STX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 24726755, 29266534; Phenotypes: Microvillus inclusion disease, congenital diarrheal disorder; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intestinal failure or congenital diarrhoea v0.5 STX3 Anna de Burca Deleted their review
Intestinal failure or congenital diarrhoea v0.5 STX3 Anna de Burca reviewed gene: STX3: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 24726755; Phenotypes: mi; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intestinal failure or congenital diarrhoea v0.5 STX3 Anna de Burca Deleted their review
Intestinal failure or congenital diarrhoea v0.5 STX3 Anna de Burca reviewed gene: STX3: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 24726755; Phenotypes: Microvillus inclusion disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intestinal failure or congenital diarrhoea v0.5 STX3 Anna de Burca Deleted their review
Intestinal failure or congenital diarrhoea v0.5 STX3 Anna de Burca reviewed gene: STX3: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 24726755; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intestinal failure or congenital diarrhoea v0.5 STX3 Anna de Burca Deleted their review
Intestinal failure or congenital diarrhoea v0.5 STX3 Anna de Burca reviewed gene: STX3: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 24726755; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intestinal failure or congenital diarrhoea v0.4 STX3 Ivone Leong Source Expert Review Green was added to STX3.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Intestinal failure or congenital diarrhoea v0.3 STX3 Ivone Leong reviewed gene: STX3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Intestinal failure or congenital diarrhoea v0.2 STX3 Ivone Leong gene: STX3 was added
gene: STX3 was added to Intestinal failure. Sources: NHS GMS
Mode of inheritance for gene: STX3 was set to