Activity

Filter

Cancel
Date Panel Item Activity
11 actions
Disorders of immune dysregulation v2.0 GATA3 Gene migrated from ENSG00000107485 to ENSG00000107485 (gene set migration)
Disorders of immune dysregulation v0.70 GATA3 Zornitza Stark Mode of pathogenicity for gene: GATA3 was changed from None to Other
Disorders of immune dysregulation v0.69 GATA3 Zornitza Stark Marked gene: GATA3 as ready
Disorders of immune dysregulation v0.69 GATA3 Zornitza Stark Added comment: Comment when marking as ready: Dominant negative effect proposed.
Disorders of immune dysregulation v0.69 GATA3 Zornitza Stark Gene: gata3 has been classified as Amber List (Moderate Evidence).
Disorders of immune dysregulation v0.69 GATA3 Zornitza Stark Marked gene: GATA3 as ready
Disorders of immune dysregulation v0.69 GATA3 Zornitza Stark Gene: gata3 has been classified as Amber List (Moderate Evidence).
Disorders of immune dysregulation v0.69 GATA3 Zornitza Stark Phenotypes for gene: GATA3 were changed from Hypoparathyroidism, sensorineural deafness, and renal dysplasia MIM#146255 to Immune dysregulation; Hypoparathyroidism, sensorineural deafness, and renal dysplasia MIM#146255
Disorders of immune dysregulation v0.68 GATA3 Zornitza Stark Classified gene: GATA3 as Amber List (moderate evidence)
Disorders of immune dysregulation v0.68 GATA3 Zornitza Stark Gene: gata3 has been classified as Amber List (Moderate Evidence).
Disorders of immune dysregulation v0.67 GATA3 Elena Savva gene: GATA3 was added
gene: GATA3 was added to Disorders of immune dysregulation. Sources: Literature
Mode of inheritance for gene: GATA3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: GATA3 were set to PMID: 31238969
Phenotypes for gene: GATA3 were set to Hypoparathyroidism, sensorineural deafness, and renal dysplasia MIM#146255
Review for gene: GATA3 was set to AMBER
gene: GATA3 was marked as current diagnostic
Added comment: PMID: 31238969: patient with protein elongation variant p.(M401Vfs*106) has an additional phenotype of juvenile idiopathic arthritis. Functional studies on the variant support pathogenicity, and analysis of patient cells indicate defective T helper cell differentiation and cytokine production.
Sources: Literature