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Vascular Malformations_Somatic v1.7 GNB2 Zornitza Stark gene: GNB2 was added
gene: GNB2 was added to Vascular Malformations_Somatic. Sources: Literature
somatic tags were added to gene: GNB2.
Mode of inheritance for gene: GNB2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: GNB2 were set to 34124757
Phenotypes for gene: GNB2 were set to Sturge-Weber syndrome, somatic, mosaic
Mode of pathogenicity for gene: GNB2 was set to Other
Review for gene: GNB2 was set to RED
Added comment: PMID: 34124757 Fjaer et al 2021 report 1 case of a patient with phenotypic features of Sturge–Weber syndrome (skin legion on left eyelid, nose and brow, mild intellectual disability, refractory eplipsy, left-sided leptomeningeal vascular malformation and atrophy, no eye abnormality) and a variant in GNB2 (NM_005273.3):c.232A>G:p.Lys78Glu, which was present in 6% of the reads from the lesional dermis and 21% of the reads in an endothelial culture from the biopsy, but only present at 0.15% of the reads in non-lesional dermis. The patient was negative for the GNAQ R183Q variant more frequently associated with Sturge–Weber syndrome.
Sources: Literature
Vascular Malformations_Somatic v0.9 GNAQ Bryony Thompson changed review comment from: Comment on list classification: Somatic mutation only causes vascular malformations. Not really suitable for a germline testing panel.; to: Comment on list classification: Somatic mutation only causes vascular malformations.
Vascular Malformations_Somatic v0.2 GNAQ Zornitza Stark Marked gene: GNAQ as ready
Vascular Malformations_Somatic v0.2 GNAQ Zornitza Stark Gene: gnaq has been classified as Green List (High Evidence).
Vascular Malformations_Somatic v0.2 GNAQ Zornitza Stark Tag somatic tag was added to gene: GNAQ.
Vascular Malformations_Somatic v0.0 GNAQ Zornitza Stark gene: GNAQ was added
gene: GNAQ was added to Vascular Malformations_Somatic. Sources: Expert list,Expert Review Green
Mode of inheritance for gene: GNAQ was set to Other
Publications for gene: GNAQ were set to 30920161
Phenotypes for gene: GNAQ were set to Sturge-Weber syndrome, somatic, mosaic 185300; Capillary malformations, congenital, 1, somatic, mosaic 163000; Phacomatosis pigmentovascularis