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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1700",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1698",
"results": [
{
"created": "2020-07-30T19:52:04.354314+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RET as ready",
"entity_name": "RET",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:52:04.344046+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ret has been classified as Green List (High Evidence).",
"entity_name": "RET",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:51:57.734223+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RET were changed from to Multiple endocrine neoplasia IIA, MIM# 171400; Multiple endocrine neoplasia IIB, MIM# 162300",
"entity_name": "RET",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:51:44.280479+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RET was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RET",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:51:27.432955+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RET: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Multiple endocrine neoplasia IIA, MIM# 171400, Multiple endocrine neoplasia IIB, MIM# 162300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RET",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:50:43.999361+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTEN as ready",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:50:43.990993+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pten has been classified as Green List (High Evidence).",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:50:39.442762+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTEN were changed from to Cowden syndrome 1, MIM# 158350",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:50:28.518255+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PTEN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:50:13.832675+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PTEN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cowden syndrome 1, MIM# 158350; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:49:43.334921+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKAG2 as ready",
"entity_name": "PRKAG2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:49:43.326891+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkag2 has been classified as Green List (High Evidence).",
"entity_name": "PRKAG2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:49:41.323097+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRKAG2 were changed from to Cardiomyopathy, hypertrophic 6, MIM# 600858",
"entity_name": "PRKAG2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:49:31.307705+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRKAG2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKAG2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:49:21.177848+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRKAG2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, hypertrophic 6, MIM# 600858; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRKAG2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:48:30.567766+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PMS2 as ready",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:48:30.558500+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pms2 has been classified as Green List (High Evidence).",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:48:28.421679+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PMS2 were changed from to Colorectal cancer, hereditary nonpolyposis, type 4, MIM# 614337",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:48:18.705000+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PMS2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:48:08.827243+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PMS2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Colorectal cancer, hereditary nonpolyposis, type 4, MIM# 614337; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:47:39.487624+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PKP2 as ready",
"entity_name": "PKP2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:47:39.470466+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pkp2 has been classified as Green List (High Evidence).",
"entity_name": "PKP2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:47:33.823772+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PKP2 were changed from to Arrhythmogenic right ventricular dysplasia 9, MIM# 609040",
"entity_name": "PKP2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:47:24.337010+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PKP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PKP2",
"entity_type": "gene"
},
{
"created": "2020-07-30T19:47:11.409719+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PKP2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Arrhythmogenic right ventricular dysplasia 9, MIM# 609040; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PKP2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:57:28.479170+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PCSK9 as ready",
"entity_name": "PCSK9",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:57:28.468383+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pcsk9 has been classified as Green List (High Evidence).",
"entity_name": "PCSK9",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:57:26.358405+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PCSK9 were changed from to Hypercholesterolemia, familial, 3, MIM# 603776",
"entity_name": "PCSK9",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:57:20.063496+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PCSK9 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PCSK9",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:57:11.648522+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PCSK9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypercholesterolemia, familial, 3, MIM# 603776; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PCSK9",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:56:41.230660+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OTC as ready",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:56:41.220876+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: otc has been classified as Green List (High Evidence).",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:56:39.416542+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OTC were changed from to Ornithine transcarbamylase deficiency, MIM# 311250",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:56:31.412368+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OTC was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:56:21.866278+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OTC: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ornithine transcarbamylase deficiency, MIM# 311250; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:55:54.537080+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NF2 as ready",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:55:54.525851+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nf2 has been classified as Green List (High Evidence).",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:55:52.802273+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NF2 were changed from to Neurofibromatosis, type 2, MIM# 101000",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:55:45.165292+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NF2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:55:36.376402+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurofibromatosis, type 2, MIM# 101000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:55:10.456580+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYL3 as ready",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:55:10.445982+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myl3 has been classified as Green List (High Evidence).",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:55:07.827178+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYL3 were changed from to Cardiomyopathy, hypertrophic, 8, MIM# 608751",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:54:50.806944+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYL3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:54:40.580311+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYL3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, hypertrophic, 8, MIM# 608751; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYL3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:54:04.988139+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYL2 as ready",
"entity_name": "MYL2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:54:04.965185+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myl2 has been classified as Green List (High Evidence).",
"entity_name": "MYL2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:54:03.261283+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYL2 were changed from to Cardiomyopathy, hypertrophic, 10, MIM# 608758",
"entity_name": "MYL2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:53:53.795212+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYL2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYL2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:53:36.812539+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYL2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, hypertrophic, 10, MIM# 608758; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYL2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:53:11.965479+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYH7 as ready",
"entity_name": "MYH7",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:53:11.957029+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myh7 has been classified as Green List (High Evidence).",
"entity_name": "MYH7",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:53:09.838243+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYH7 were changed from to Cardiomyopathy, dilated, 1S, MIM# 613426; Cardiomyopathy, hypertrophic, 1, MIM# 192600",
"entity_name": "MYH7",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:53:02.206327+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYH7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH7",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:52:52.321009+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYH7: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, dilated, 1S, MIM# 613426, Cardiomyopathy, hypertrophic, 1, MIM# 192600; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH7",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:52:17.782459+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYH11 as ready",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:52:17.774281+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myh11 has been classified as Green List (High Evidence).",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:52:15.975626+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYH11 were changed from to Aortic aneurysm, familial thoracic 4, MIM# 132900",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:52:09.137189+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYH11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:52:00.008079+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYH11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aortic aneurysm, familial thoracic 4, MIM# 132900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH11",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:51:33.263837+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYBPC3 as ready",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:51:33.255388+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mybpc3 has been classified as Green List (High Evidence).",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:51:31.486431+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYBPC3 were changed from to Cardiomyopathy, dilated, 1MM, MIM# 615396; Cardiomyopathy, hypertrophic, 4, MIM# 115197; Left ventricular noncompaction 10, MIM# 615396",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:51:24.674076+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYBPC3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:51:13.495353+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYBPC3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, dilated, 1MM, MIM# 615396, Cardiomyopathy, hypertrophic, 4, MIM# 115197, Left ventricular noncompaction 10, MIM# 615396; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:50:27.730766+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MUTYH as ready",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:50:27.721018+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mutyh has been classified as Green List (High Evidence).",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:50:25.929153+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MUTYH were changed from to Adenomas, multiple colorectal, MIM# 608456",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:50:12.825259+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MUTYH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:50:03.200019+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MUTYH: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Adenomas, multiple colorectal, MIM# 608456; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:28:46.033932+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MSH6 as ready",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:28:46.023515+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: msh6 has been classified as Green List (High Evidence).",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:28:43.554986+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MSH6 were changed from to Colorectal cancer, hereditary nonpolyposis, type 5, MIM# 614350",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:28:35.232330+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MSH6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:28:25.759292+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MSH6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Colorectal cancer, hereditary nonpolyposis, type 5, MIM# 614350; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:27:59.012166+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MSH2 as ready",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:27:59.004328+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: msh2 has been classified as Green List (High Evidence).",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:27:57.178123+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MSH2 were changed from to Colorectal cancer, hereditary nonpolyposis, type 1, MIM# 120435",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:27:45.115004+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MSH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:27:35.351674+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MSH2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Colorectal cancer, hereditary nonpolyposis, type 1, MIM# 120435; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:27:04.839386+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MLH1 as ready",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:27:04.830683+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlh1 has been classified as Green List (High Evidence).",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:27:02.441752+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MLH1 were changed from to Colorectal cancer, hereditary nonpolyposis, type 2, MIM# 609310",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:26:54.725206+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MLH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:26:45.959296+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MLH1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Colorectal cancer, hereditary nonpolyposis, type 2, MIM# 609310; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:26:15.451132+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MEN1 as ready",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:26:15.443256+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: men1 has been classified as Green List (High Evidence).",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:26:12.110673+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MEN1 were changed from to Multiple endocrine neoplasia 1, MIM# 131100",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:26:05.442042+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MEN1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:25:56.423396+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MEN1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Multiple endocrine neoplasia 1, MIM# 131100; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:25:31.519424+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LMNA as ready",
"entity_name": "LMNA",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:25:31.510431+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lmna has been classified as Green List (High Evidence).",
"entity_name": "LMNA",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:25:29.506050+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LMNA were changed from to Cardiomyopathy, dilated, 1A, MIM# 115200",
"entity_name": "LMNA",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:25:10.169175+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LMNA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "LMNA",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:25:01.896259+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LMNA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, dilated, 1A, MIM# 115200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "LMNA",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:24:33.486053+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LDLR as ready",
"entity_name": "LDLR",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:24:33.478041+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ldlr has been classified as Green List (High Evidence).",
"entity_name": "LDLR",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:24:31.365023+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LDLR were changed from to Hypercholesterolemia, familial, 1, MIM# 143890",
"entity_name": "LDLR",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:24:19.376946+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LDLR was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "LDLR",
"entity_type": "gene"
},
{
"created": "2020-07-30T18:24:10.790243+10:00",
"panel_name": "Additional findings_Adult",
"panel_id": 221,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LDLR: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypercholesterolemia, familial, 1, MIM# 143890; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "LDLR",
"entity_type": "gene"
}
]
}