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| COVID-19 research v0.182 | ITPKB | Ivone Leong Classified gene: ITPKB as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| COVID-19 research v0.182 | ITPKB | Ivone Leong Gene: itpkb has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| COVID-19 research v0.181 | ITPKB |
Ivone Leong gene: ITPKB was added gene: ITPKB was added to Viral susceptibility. Sources: Expert list Mode of inheritance for gene: ITPKB was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ITPKB were set to 31987846; 14517551 Phenotypes for gene: ITPKB were set to Severe combined immunodeficiency, absent T cells, present B cells and NK cells Review for gene: ITPKB was set to AMBER Added comment: "Single individual with homozygous bi-allelic LoF variant reported. Sources: Literature Zornitza Stark (Australian Genomics), 1 May 2020" - review copied from Primary immunodeficiency panel (v2.147). "Comment on list classification: Gene added by Zornitza Stark (Australian Genomics) with a recommended Red gene rating based on evidence provided. PMID: 31987846 describes a patient born of consanguineous Egyptian parents. The patient failed to thrive and had persistent thrush shortly after birth, recurrent pneumonias beginning at age 2 months, and Klebsiella pneumoniae skin abscesses at age 6 and 10 months. She had severe SCID. PMID: 14517551 is a itpkb-/- mouse. Knockout of the gene caused a severe T cell deficiency. Based on these 2 pieces of information the gene has been given an Amber gene rating. Ivone Leong (Genomics England Curator), 5 May 2020" - review copied from Primary immunodeficiency panel (v2.147). Sources: Expert list |
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