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"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1115",
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{
"created": "2021-11-28T17:37:57.705233+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP21A2 were changed from Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency; Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency to Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, MIM# 201910",
"entity_name": "CYP21A2",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:37:41.340473+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP21A2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, MIM# 201910; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP21A2",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:36:28.450999+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP1B1 as ready",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:36:28.438835+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp1b1 has been classified as Green List (High Evidence).",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:36:25.060063+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP1B1 were changed from PRIMARY CONGENITAL GLAUCOMA TYPE 3A to Anterior segment dysgenesis 6, multiple subtypes, MIM# 617315; Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, MIM# 231300",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:36:12.911090+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.752",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP1B1 were set to ",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:36:01.401551+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP1B1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:35:45.353841+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP1B1: Rating: GREEN; Mode of pathogenicity: None; Publications: 32499604, 32224865; Phenotypes: Anterior segment dysgenesis 6, multiple subtypes, MIM# 617315, Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, MIM# 231300; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CYP1B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:32:19.750978+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP17A1 as ready",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:32:19.733594+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp17a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:32:17.504032+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP17A1 were changed from to 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:31:54.921364+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP17A1 were set to ",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:31:26.346764+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP17A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:31:02.099920+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP17A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 2843762, 14671162, 2026124; Phenotypes: 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:30:27.554881+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9915",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP17A1 as ready",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:30:27.544341+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9915",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp17a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:30:21.166408+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9915",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP17A1 were changed from to 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:30:04.654014+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9914",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP17A1 were set to ",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:29:45.996856+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9913",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP17A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:29:30.261266+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9912",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP17A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 2843762, 14671162, 2026124; Phenotypes: 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:28:37.015860+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP17A1 as ready",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:28:37.006474+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp17a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:28:32.309647+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP17A1 were changed from 17-alpha-hydroxylase/17,20-lyase deficiency; 17,20-lyase deficiency, isolated to 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:28:17.684040+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP17A1 were set to ",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:28:02.775170+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP17A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 2843762, 14671162, 2026124; Phenotypes: 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:25:43.475430+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11B1 as ready",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:25:43.460612+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11b1 has been classified as Green List (High Evidence).",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:25:41.171141+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11B1 were changed from to Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:25:17.303395+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11B1 were set to ",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:24:54.494323+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP11B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:24:23.453515+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP11B1: Rating: GREEN; Mode of pathogenicity: None; Publications: 8768848; Phenotypes: Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:23:40.623044+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9912",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11B1 as ready",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:23:40.613722+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9912",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11b1 has been classified as Green List (High Evidence).",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:23:33.446412+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9912",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11B1 were changed from to Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010; Aldosteronism, glucocorticoid-remediable, MIM# 103900",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:23:14.857320+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9911",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11B1 were set to ",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:22:55.486846+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9910",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP11B1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:22:35.726381+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9909",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP11B1: Rating: GREEN; Mode of pathogenicity: None; Publications: 8768848, 1731223, 29703198; Phenotypes: Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010, Aldosteronism, glucocorticoid-remediable, MIM# 103900; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:20:02.188454+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11B1 as ready",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:20:02.168649+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11b1 has been classified as Green List (High Evidence).",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:19:58.625214+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11B1 were changed from Aldosteronism, glucocorticoid-remediable 103900; Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency 202010 to Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:19:46.383299+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11B1 were set to ",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:19:36.479073+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP11B1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:19:21.662097+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP11B1: Rating: GREEN; Mode of pathogenicity: None; Publications: 8768848; Phenotypes: Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:15:52.874220+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11A1 as ready",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:15:52.863313+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11a1 has been classified as Red List (Low Evidence).",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:15:49.536812+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11A1 were changed from to Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:15:19.513655+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.341",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11A1 were set to ",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:14:50.946852+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.340",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP11A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:14:28.369439+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11A1 as ready",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:14:28.359113+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:14:27.276969+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.339",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CYP11A1 as Red List (low evidence)",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:14:27.267441+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.339",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11a1 has been classified as Red List (Low Evidence).",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:14:01.053554+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11A1 were changed from to Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:13:56.472000+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.338",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP11A1: Rating: RED; Mode of pathogenicity: None; Publications: 12161514, 16705068, 18182448, 28425981; Phenotypes: Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:13:31.823441+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11A1 were set to ",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:13:08.480123+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9909",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11A1 as ready",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:13:08.468200+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9909",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:12:57.867005+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP11A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:12:29.450377+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9909",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11A1 were changed from to Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:12:27.453849+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP11A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12161514, 16705068, 18182448, 28425981; Phenotypes: Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:12:12.266438+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9908",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11A1 were set to ",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:11:40.101049+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9907",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP11A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:11:16.656364+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9906",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP11A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12161514, 16705068, 18182448, 28425981; Phenotypes: Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:10:30.628594+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: CYP11A1: Changed publications: 12161514, 16705068, 18182448, 28425981",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:10:17.649244+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP11A1 as ready",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:10:17.638892+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp11a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:10:02.101399+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP11A1 were changed from Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete 613743 to Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:09:49.837576+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP11A1 were set to 28425981",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:09:34.579183+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP11A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12161514, 16705068, 18182448; Phenotypes: Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:06:46.692756+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4316",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CWC27 as ready",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:06:46.680860+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4316",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cwc27 has been classified as Green List (High Evidence).",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:06:43.097206+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4316",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CWC27 were changed from to Retinitis pigmentosa with or without skeletal anomalies, MIM# 250410",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:06:09.901159+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4315",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CWC27 were set to ",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:05:39.229751+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CWC27 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:05:12.653788+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CWC27: Rating: GREEN; Mode of pathogenicity: None; Publications: 28285769, 31481716; Phenotypes: Retinitis pigmentosa with or without skeletal anomalies, MIM# 250410; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:04:41.183276+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9906",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CWC27 as ready",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:04:41.172797+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9906",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cwc27 has been classified as Green List (High Evidence).",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:04:33.677267+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9906",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CWC27 were changed from to Retinitis pigmentosa with or without skeletal anomalies, MIM# 250410",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:04:15.342637+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9905",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CWC27 were set to ",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:03:58.408031+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9904",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CWC27 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:03:40.970021+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9903",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CWC27: Rating: GREEN; Mode of pathogenicity: None; Publications: 28285769, 31481716; Phenotypes: Retinitis pigmentosa with or without skeletal anomalies, MIM# 250410; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:03:04.870774+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CWC27 as ready",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:03:04.859884+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cwc27 has been classified as Green List (High Evidence).",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:03:00.773904+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CWC27 were changed from Retinitis pigmentosa, skeletal anomalies and intellectual disability to Retinitis pigmentosa with or without skeletal anomalies, MIM# 250410",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:02:47.954748+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CWC27 were set to 28285769",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T17:02:33.231917+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CWC27: Rating: GREEN; Mode of pathogenicity: None; Publications: 28285769, 31481716; Phenotypes: Retinitis pigmentosa with or without skeletal anomalies, MIM# 250410; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2021-11-28T16:56:53.418204+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CUL7 as ready",
"entity_name": "CUL7",
"entity_type": "gene"
},
{
"created": "2021-11-28T16:56:53.408155+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cul7 has been classified as Green List (High Evidence).",
"entity_name": "CUL7",
"entity_type": "gene"
},
{
"created": "2021-11-28T16:56:49.876352+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CUL7 were changed from 3-M SYNDROME 1 to 3-M syndrome 1, MIM# 273750; Yakut short stature syndrome",
"entity_name": "CUL7",
"entity_type": "gene"
},
{
"created": "2021-11-28T16:56:38.423706+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CUL7 were set to ",
"entity_name": "CUL7",
"entity_type": "gene"
},
{
"created": "2021-11-28T16:56:23.696020+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CUL7: Rating: GREEN; Mode of pathogenicity: None; Publications: 16142236, 19225462, 17675530; Phenotypes: 3-M syndrome 1, MIM# 273750, Yakut short stature syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CUL7",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:07:17.994827+11:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PPIB as ready",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:07:17.984176+11:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ppib has been classified as Green List (High Evidence).",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:07:15.594971+11:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PPIB were changed from to Osteogenesis imperfecta, type IX, MIM# 259440",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:06:45.534307+11:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PPIB were set to ",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:06:22.114091+11:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PPIB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:05:57.340579+11:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PPIB: Rating: GREEN; Mode of pathogenicity: None; Publications: 19781681, 32392875; Phenotypes: Osteogenesis imperfecta, type IX, MIM# 259440; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:05:24.030617+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9903",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PPIB as ready",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:05:24.020435+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9903",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ppib has been classified as Green List (High Evidence).",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2021-11-26T20:05:16.941173+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9903",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PPIB were changed from to Osteogenesis imperfecta, type IX, MIM# 259440",
"entity_name": "PPIB",
"entity_type": "gene"
}
]
}