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Congenital Heart Defect v1.0 TMEM260 Gene migrated from ENSG00000070269 to ENSG00000070269 (gene set migration)
Congenital Heart Defect v0.158 TMEM260 Zornitza Stark changed review comment from: Seven unrelated families with complex severe congenital heart disease.
Sources: Expert list; to: Seven unrelated families with complex severe congenital heart disease. Clinical features: ventricular septal defects (12/12), mostly secondary to truncus arteriosus (10/12), elevated creatinine levels (6/12), horse-shoe kidneys (1/12) and renal cysts (1/12) in patients.
Sources: Expert list
Congenital Heart Defect v0.158 TMEM260 Zornitza Stark Classified gene: TMEM260 as Green List (high evidence)
Congenital Heart Defect v0.158 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Green List (High Evidence).
Congenital Heart Defect v0.157 TMEM260 Zornitza Stark changed review comment from: Two unrelated families with complex severe congenital heart disease.
Sources: Expert list; to: Seven unrelated families with complex severe congenital heart disease.
Sources: Expert list
Congenital Heart Defect v0.157 TMEM260 Zornitza Stark edited their review of gene: TMEM260: Changed rating: GREEN; Changed publications: 28318500, 34612517
Congenital Heart Defect v0.27 TMEM260 Zornitza Stark Marked gene: TMEM260 as ready
Congenital Heart Defect v0.27 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Amber List (Moderate Evidence).
Congenital Heart Defect v0.27 TMEM260 Zornitza Stark Classified gene: TMEM260 as Amber List (moderate evidence)
Congenital Heart Defect v0.27 TMEM260 Zornitza Stark Gene: tmem260 has been classified as Amber List (Moderate Evidence).
Congenital Heart Defect v0.26 TMEM260 Zornitza Stark gene: TMEM260 was added
gene: TMEM260 was added to Congenital Heart Defect. Sources: Expert list
Mode of inheritance for gene: TMEM260 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TMEM260 were set to 28318500
Phenotypes for gene: TMEM260 were set to Structural heart defects and renal anomalies syndrome, MIM# 617478
Review for gene: TMEM260 was set to AMBER
Added comment: Two unrelated families with complex severe congenital heart disease.
Sources: Expert list