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Date	Panel	Item	Activity
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16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.40	COQ7	Chirag Patel Classified gene: COQ7 as Amber List (moderate evidence)
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.40	COQ7	Chirag Patel Gene: coq7 has been classified as Amber List (Moderate Evidence).
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.40	COQ7	Chirag Patel Classified gene: COQ7 as Amber List (moderate evidence)
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.40	COQ7	Chirag Patel Gene: coq7 has been classified as Amber List (Moderate Evidence).
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.40	COQ7	Chirag Patel Classified gene: COQ7 as Amber List (moderate evidence)
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.40	COQ7	Chirag Patel Gene: coq7 has been classified as Amber List (Moderate Evidence).
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.39	COQ7	Chirag Patel Classified gene: COQ7 as Amber List (moderate evidence)
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.39	COQ7	Chirag Patel Gene: coq7 has been classified as Amber List (Moderate Evidence).
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.39	COQ7	Chirag Patel Classified gene: COQ7 as Amber List (moderate evidence)
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.39	COQ7	Chirag Patel Gene: coq7 has been classified as Amber List (Moderate Evidence).
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.38	COQ7	Chirag Patel changed review comment from: only one patient with mito disease and happened to have hypoplastic kidneys.; to: only 2 patients reported
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.38	COQ7	Chirag Patel Classified gene: COQ7 as Red List (low evidence)
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.38	COQ7	Chirag Patel Gene: coq7 has been classified as Red List (Low Evidence).
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.37	COQ7	Chirag Patel reviewed gene: COQ7: Rating: RED; Mode of pathogenicity: None; Publications: PubMed: 26084283; Phenotypes: ?Coenzyme Q10 deficiency, primary, 8, OMIM #616733; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
28 Nov 2019	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.8	COQ7	Zornitza Stark Marked gene: COQ7 as ready
28 Nov 2019	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.8	COQ7	Zornitza Stark Gene: coq7 has been classified as Green List (High Evidence).
28 Nov 2019	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.8	COQ7	Zornitza Stark Classified gene: COQ7 as Green List (high evidence)
28 Nov 2019	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.8	COQ7	Zornitza Stark Gene: coq7 has been classified as Green List (High Evidence).
28 Nov 2019	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.7	COQ7	Zornitza Stark gene: COQ7 was added gene: COQ7 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list Mode of inheritance for gene: COQ7 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: COQ7 were set to 31240163; 28409910; 26084283 Phenotypes for gene: COQ7 were set to Coenzyme Q10 deficiency, primary, 8, MIM#616733 Review for gene: COQ7 was set to GREEN Added comment: Three individuals described in the literature, renal disease prominent in at least two. Sources: Expert list