Differences of Sex Development
Gene: SART3EnsemblGeneIds (GRCh38): ENSG00000075856
EnsemblGeneIds (GRCh37): ENSG00000075856
OMIM: 611684, Gene2Phenotype
SART3 is in 4 panels
1 review
Daniel Flanagan (Victorian Clinical Genetics Services)
Nine individuals from six families presenting with intellectual disability, global developmental delay, a subset of brain anomalies, together with gonadal dysgenesis in 46,XY individuals. Additionally, two individuals had seizures and two had epileptiform activity reported on EEG.
Human induced pluripotent stem cells carrying patient variants in SART3 show disruption to multiple signalling pathways, upregulation of spliceosome components and demonstrate aberrant gonadal and neuronal differentiation in vitro.
Sources: Expert listCreated: 6 Jul 2023, 3:09 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder (MONDO#0700092), SART3-related; 46,XY disorder of sex development (MONDO:0020040), SART3-related
Publications
- PMID: 37296101
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Phenotypes
-
- Neurodevelopmental disorder (MONDO#0700092), SART3-related
- 46,XY disorder of sex development (MONDO:0020040), SART3-related
- OMIM
- 611684
- Clinvar variants
- Variants in SART3
- Penetrance
- None
- Publications
-
- PMID: 37296101
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Krithika Murali (Victorian Clinical Genetics Services)Gene: sart3 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Krithika Murali (Victorian Clinical Genetics Services)Gene: sart3 has been removed from the panel.
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Daniel Flanagan (Victorian Clinical Genetics Services)gene: SART3 was added gene: SART3 was added to Differences of Sex Development. Sources: Expert list Mode of inheritance for gene: SART3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SART3 were set to PMID: 37296101 Phenotypes for gene: SART3 were set to Neurodevelopmental disorder (MONDO#0700092), SART3-related; 46,XY disorder of sex development (MONDO:0020040), SART3-related Review for gene: SART3 was set to GREEN