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Inflammatory bowel disease v1.0 STXBP3 Gene migrated from ENSG00000116266 to ENSG00000116266 (gene set migration)
Inflammatory bowel disease v0.125 STXBP3 Zornitza Stark Phenotypes for gene: STXBP3 were changed from Very Early Onset Inflammatory Bowel Disease; Bilateral Sensorineural Hearing Loss; Immune Dysregulation to Inborn error of immunity, MONDO:0003778, STXBP3-related
Inflammatory bowel disease v0.124 STXBP3 Zornitza Stark edited their review of gene: STXBP3: Changed phenotypes: Inborn error of immunity, MONDO:0003778, STXBP3-related
Inflammatory bowel disease v0.57 STXBP3 Zornitza Stark Classified gene: STXBP3 as Green List (high evidence)
Inflammatory bowel disease v0.57 STXBP3 Zornitza Stark Gene: stxbp3 has been classified as Green List (High Evidence).
Inflammatory bowel disease v0.56 STXBP3 Zornitza Stark Classified gene: STXBP3 as Green List (high evidence)
Inflammatory bowel disease v0.56 STXBP3 Zornitza Stark Gene: stxbp3 has been classified as Green List (High Evidence).
Inflammatory bowel disease v0.55 STXBP3 Zornitza Stark Marked gene: STXBP3 as ready
Inflammatory bowel disease v0.55 STXBP3 Zornitza Stark Gene: stxbp3 has been classified as Red List (Low Evidence).
Inflammatory bowel disease v0.55 STXBP3 Zornitza Stark gene: STXBP3 was added
gene: STXBP3 was added to Inflammatory bowel disease. Sources: Literature
Mode of inheritance for gene: STXBP3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: STXBP3 were set to 33891011
Phenotypes for gene: STXBP3 were set to Very Early Onset Inflammatory Bowel Disease; Bilateral Sensorineural Hearing Loss; Immune Dysregulation
Review for gene: STXBP3 was set to GREEN
Added comment: 10 individuals from 5 families reported.
Sources: Literature