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Fetal anomalies v1.836 KIAA0753 Arina Puzriakova Tag for-review was removed from gene: KIAA0753.
Fetal anomalies v1.836 KIAA0753 Arina Puzriakova commented on gene: KIAA0753: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Fetal anomalies v1.835 KIAA0753 Arina Puzriakova Source Expert Review Green was added to KIAA0753.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Fetal anomalies v1.238 KIAA0753 Arina Puzriakova Classified gene: KIAA0753 as Amber List (moderate evidence)
Fetal anomalies v1.238 KIAA0753 Arina Puzriakova Added comment: Comment on list classification: New gene added by Rhiannon Mellis (GOSH). Following curation and clinical review it has been agreed that the associated phenotype is fetally-relevant and therefore this gene should be promoted to Green at the next GMS panel update (added 'for-review' tag)
Fetal anomalies v1.238 KIAA0753 Arina Puzriakova Gene: kiaa0753 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v1.237 KIAA0753 Arina Puzriakova Publications for gene: KIAA0753 were set to
Fetal anomalies v1.236 KIAA0753 Arina Puzriakova Phenotypes for gene: KIAA0753 were changed from ?Orofaciodigital syndrome XV to ?Orofaciodigital syndrome XV, OMIM:617127; Orofaciodigital syndrome XV, MONDO:0014932
Fetal anomalies v1.235 KIAA0753 Arina Puzriakova Tag for-review tag was added to gene: KIAA0753.
Fetal anomalies v1.214 KIAA0753 Rhiannon Mellis gene: KIAA0753 was added
gene: KIAA0753 was added to Fetal anomalies. Sources: Expert list
Mode of inheritance for gene: KIAA0753 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: KIAA0753 were set to ?Orofaciodigital syndrome XV
Review for gene: KIAA0753 was set to GREEN
Added comment: This gene and phenotype were reviewed during meetings at Great Ormond Street hospital in October 2020. This gene has a Green evidence rating on at least one other related PanelApp panel. Clinical review and curation was performed by Lyn Chitty, Rhiannon Mellis, and Richard Scott. Outcome of review: Confirmed that phenotype is fetally-relevant: add to the Fetal anomalies panel as a Green gene.

Green on related panel(s): Cystic renal disease (super panel); Rare multisystem ciliopathy Super panel; Skeletal dysplasia
Sources: Expert list