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Fetal anomalies v1.836 DYNC2LI1 Arina Puzriakova Tag for-review was removed from gene: DYNC2LI1.
Fetal anomalies v1.836 DYNC2LI1 Arina Puzriakova commented on gene: DYNC2LI1: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Fetal anomalies v1.835 DYNC2LI1 Arina Puzriakova Source Expert Review Green was added to DYNC2LI1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Fetal anomalies v1.392 DYNC2LI1 Arina Puzriakova Classified gene: DYNC2LI1 as Amber List (moderate evidence)
Fetal anomalies v1.392 DYNC2LI1 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 v1.392 DYNC2LI1 Arina Puzriakova Gene: dync2li1 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v1.391 DYNC2LI1 Arina Puzriakova Tag for-review tag was added to gene: DYNC2LI1.
Fetal anomalies v1.215 DYNC2LI1 Rhiannon Mellis gene: DYNC2LI1 was added
gene: DYNC2LI1 was added to Fetal anomalies. Sources: Expert list
Mode of inheritance for gene: DYNC2LI1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: DYNC2LI1 were set to Short-rib thoracic dysplasia 15 with polydactyly, 617088
Review for gene: DYNC2LI1 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): Clefting; Rare multisystem ciliopathy Super panel; Skeletal dysplasia; Thoracic dystrophies
Sources: Expert list