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Fetal anomalies v0.3992 SLIT2 Zornitza Stark Marked gene: SLIT2 as ready
Fetal anomalies v0.3992 SLIT2 Zornitza Stark Gene: slit2 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3992 SLIT2 Zornitza Stark Classified gene: SLIT2 as Amber List (moderate evidence)
Fetal anomalies v0.3992 SLIT2 Zornitza Stark Gene: slit2 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3502 SLIT2 Krithika Murali gene: SLIT2 was added
gene: SLIT2 was added to Fetal anomalies. Sources: Literature
Mode of inheritance for gene: SLIT2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SLIT2 were set to 26026792; 15130495
Phenotypes for gene: SLIT2 were set to CAKUT; vesicoureteric reflux
Review for gene: SLIT2 was set to AMBER
Added comment: PMID 26026792 Hwang et al 2019 - identified three unrelated individuals with CAKUT and different heterozygous SLIT2 missense mutations.
- 1 patient presented with multiple bilateral subcortical renal cysts
- 1 patient presented with multicystic dysplastic kidneys
- 1 patient had right renal agenesis

Authors provide supportive variant-specific mouse models.

PMID: 34059960 Liu et al 2021 - 3 unrelated children from a Chinese Kidney Disease Database with vesicoureteric reflux had SLIT3 VUS identified

PMID 19350278 Zu et al 2009 - x2 unrelated individuals with SLIT2 variants - not segregating with disease in either family
Sources: Literature