Microcephaly
Gene: SARSEnsemblGeneIds (GRCh38): ENSG00000031698
EnsemblGeneIds (GRCh37): ENSG00000031698
OMIM: 607529, Gene2Phenotype
SARS is in 5 panels
1 review
Ain Roesley (Victorian Clinical Genetics Services)
Total of 3 families
Sources: LiteratureCreated: 4 Aug 2022, 7:03 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
neurodevelopmental disorder MONDO#070009, SARS1-related
Publications
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- neurodevelopmental disorder MONDO#070009, SARS1-related
- OMIM
- 607529
- Clinvar variants
- Variants in SARS
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: sars has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Ain Roesley (Victorian Clinical Genetics Services)Gene: sars has been classified as Red List (Low Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Ain Roesley (Victorian Clinical Genetics Services)gene: SARS was added gene: SARS was added to Microcephaly. Sources: Literature Mode of inheritance for gene: SARS was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SARS were set to 35790048; 28236339; 34570399 Phenotypes for gene: SARS were set to neurodevelopmental disorder MONDO#070009, SARS1-related Review for gene: SARS was set to GREEN gene: SARS was marked as current diagnostic