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Bone Marrow Failure v0.169 STN1 Zornitza Stark Publications for gene: STN1 were set to 27432940
Bone Marrow Failure v0.168 STN1 Zornitza Stark Marked gene: STN1 as ready
Bone Marrow Failure v0.168 STN1 Zornitza Stark Added comment: Comment when marking as ready: Promoted to Green, highly specific constellation of features.
Bone Marrow Failure v0.168 STN1 Zornitza Stark Gene: stn1 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.168 STN1 Zornitza Stark Classified gene: STN1 as Green List (high evidence)
Bone Marrow Failure v0.168 STN1 Zornitza Stark Gene: stn1 has been classified as Green List (High Evidence).
Bone Marrow Failure v0.167 STN1 Sue White reviewed gene: STN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 32627942; Phenotypes: Coats-plus syndrome, intracranial calcification, retinal telangiactasia, bone marrow failure; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Bone Marrow Failure v0.21 STN1 Zornitza Stark Marked gene: STN1 as ready
Bone Marrow Failure v0.21 STN1 Zornitza Stark Gene: stn1 has been classified as Amber List (Moderate Evidence).
Bone Marrow Failure v0.21 STN1 Zornitza Stark Classified gene: STN1 as Amber List (moderate evidence)
Bone Marrow Failure v0.21 STN1 Zornitza Stark Gene: stn1 has been classified as Amber List (Moderate Evidence).
Bone Marrow Failure v0.20 STN1 Zornitza Stark gene: STN1 was added
gene: STN1 was added to Bone Marrow Failure_VCGS. Sources: Expert list
Mode of inheritance for gene: STN1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: STN1 were set to 27432940
Phenotypes for gene: STN1 were set to Cerebroretinal microangiopathy with calcification and cysts 2, MIM#617341
Review for gene: STN1 was set to AMBER
Added comment: Two unrelated individuals reported with a multisystem disorder characterised by premature ageing, pancytopaenia, hypocellular bone marrow, osteopaenia, liver fibrosis, vascular telangiectasia, intracranial calcifications and leukodystrophy.
Sources: Expert list