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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1694",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1692",
"results": [
{
"created": "2020-08-02T14:45:11.488505+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TOR1A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Arthrogryposis multiplex congenita, MIM#618947; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TOR1A",
"entity_type": "gene"
},
{
"created": "2020-08-02T13:26:17.942261+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3633",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: SYNE2.",
"entity_name": "SYNE2",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:49:48.761722+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED12 as ready",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:49:48.741351+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med12 has been classified as Green List (High Evidence).",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:49:42.365142+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MED12 were changed from to MED12-related disorders",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:49:12.883620+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MED12 were set to ",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:48:48.552601+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MED12 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:47:36.707016+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIP4 as ready",
"entity_name": "TRIP4",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:47:36.698723+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trip4 has been classified as Green List (High Evidence).",
"entity_name": "TRIP4",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:47:34.008934+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIP4 were changed from to Spinal muscular atrophy with congenital bone fractures 1, MIM# 616866",
"entity_name": "TRIP4",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:47:06.796294+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIP4 were set to ",
"entity_name": "TRIP4",
"entity_type": "gene"
},
{
"created": "2020-08-01T21:46:44.357263+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIP4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIP4",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:44:32.965149+10:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOTCH2 as ready",
"entity_name": "NOTCH2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:44:32.954705+10:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: notch2 has been classified as Green List (High Evidence).",
"entity_name": "NOTCH2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:44:30.117963+10:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NOTCH2 were changed from to Alagille syndrome 2, MIM# 610205",
"entity_name": "NOTCH2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:44:01.957727+10:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NOTCH2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Alagille syndrome 2, MIM# 610205; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NOTCH2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:43:36.398094+10:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JAG1 as ready",
"entity_name": "JAG1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:43:36.389975+10:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jag1 has been classified as Green List (High Evidence).",
"entity_name": "JAG1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:43:34.168976+10:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: JAG1 were changed from to Alagille syndrome, MIM# 1 118450",
"entity_name": "JAG1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:43:06.378216+10:00",
"panel_name": "Alagille syndrome",
"panel_id": 36,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: JAG1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Alagille syndrome, MIM# 1 118450; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "JAG1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:42:02.041336+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHD as ready",
"entity_name": "SDHD",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:42:02.023664+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhd has been classified as Green List (High Evidence).",
"entity_name": "SDHD",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:41:55.447666+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SDHD were changed from to Paragangliomas 1, with or without deafness, MIM# 168000; Pheochromocytoma, MIM# 171300",
"entity_name": "SDHD",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:41:28.808561+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SDHD was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHD",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:40:58.449301+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SDHD: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Paragangliomas 1, with or without deafness, MIM# 168000, Pheochromocytoma, MIM# 171300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHD",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:40:04.236779+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHC as ready",
"entity_name": "SDHC",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:40:04.227638+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhc has been classified as Green List (High Evidence).",
"entity_name": "SDHC",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:39:58.562802+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SDHC were changed from to Paragangliomas 3, MIM# 605373",
"entity_name": "SDHC",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:39:33.611652+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SDHC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHC",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:39:07.211140+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SDHC: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Paragangliomas 3, MIM# 605373; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHC",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:38:36.144610+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHB as ready",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:38:36.136343+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhb has been classified as Green List (High Evidence).",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:38:33.853554+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SDHB were changed from to Paragangliomas 4, MIM# 115310",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:38:08.502770+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SDHB was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:37:46.450262+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SDHB: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Paragangliomas 4, MIM# 115310; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:37:09.289862+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHAF2 as ready",
"entity_name": "SDHAF2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:37:09.278422+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhaf2 has been classified as Green List (High Evidence).",
"entity_name": "SDHAF2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:36:58.161190+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SDHAF2 were changed from to Paragangliomas 2, MIM# 601650",
"entity_name": "SDHAF2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:36:37.553389+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SDHAF2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHAF2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:36:14.351619+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SDHAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Paragangliomas 2, MIM# 601650; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHAF2",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:23:21.294900+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHA as ready",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:23:21.282544+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdha has been classified as Green List (High Evidence).",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:23:18.862024+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SDHA were changed from to Paragangliomas 5, MIM# 614165",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:23:02.769927+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SDHA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:22:36.167894+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SDHA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Paragangliomas 5, MIM# 614165; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:21:33.925339+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RUNX1 as ready",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:21:33.916304+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: runx1 has been classified as Green List (High Evidence).",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:21:31.416332+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RUNX1 were changed from to Leukemia, acute myeloid, MIM# 601626",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:21:02.827371+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RUNX1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:20:40.393729+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RUNX1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukemia, acute myeloid, MIM# 601626; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:20:00.605483+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIP13 as ready",
"entity_name": "TRIP13",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:20:00.596704+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trip13 has been classified as Green List (High Evidence).",
"entity_name": "TRIP13",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:19:58.403210+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIP13 were changed from to Mosaic variegated aneuploidy syndrome 3, MIM# 617598",
"entity_name": "TRIP13",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:19:39.050909+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIP13 were set to ",
"entity_name": "TRIP13",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:19:14.889319+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIP13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIP13",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:18:48.344679+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TRIP13: Changed rating: GREEN",
"entity_name": "TRIP13",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:18:42.547644+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRIP13: Rating: ; Mode of pathogenicity: None; Publications: 28553959; Phenotypes: Mosaic variegated aneuploidy syndrome 3, MIM# 617598; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIP13",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:16:18.163319+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM127 as ready",
"entity_name": "TMEM127",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:16:18.153995+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem127 has been classified as Red List (Low Evidence).",
"entity_name": "TMEM127",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:16:16.112167+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM127 were changed from to {Pheochromocytoma, susceptibility to}, MIM# 171300",
"entity_name": "TMEM127",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:16:00.042702+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TMEM127 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TMEM127",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:15:35.945675+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TMEM127 as Red List (low evidence)",
"entity_name": "TMEM127",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:15:35.937829+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem127 has been classified as Red List (Low Evidence).",
"entity_name": "TMEM127",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:15:13.540605+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TMEM127: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Pheochromocytoma, susceptibility to}, MIM# 171300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TMEM127",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:13:43.831043+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RAD51C as Red List (low evidence)",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:13:43.820493+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rad51c has been classified as Red List (Low Evidence).",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:13:18.625273+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Two families reported, paediatric tumour risk to be established.; to: Two families reported with congenital anomalies only, paediatric tumour risk to be established.",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:13:05.346133+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: RAD51C: Changed rating: RED",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:12:12.404540+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAD51C as ready",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:12:12.393418+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rad51c has been classified as Amber List (Moderate Evidence).",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:12:09.280453+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAD51C were changed from to Fanconi anemia, complementation group O, MIM# 613390",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:11:41.066272+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAD51C were set to ",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:11:18.445012+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RAD51C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:10:54.064606+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RAD51C as Amber List (moderate evidence)",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:10:54.049339+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rad51c has been classified as Amber List (Moderate Evidence).",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:10:29.644850+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RAD51C: Rating: AMBER; Mode of pathogenicity: None; Publications: 20400963, 29278735; Phenotypes: Fanconi anemia, complementation group O, MIM# 613390; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:06:19.859577+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MUTYH as ready",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:06:19.849332+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mutyh has been classified as Red List (Low Evidence).",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:06:16.621169+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.59",
"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": "2020-08-01T18:05:51.593026+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MUTYH was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:05:38.316327+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.58",
"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": "2020-08-01T18:05:15.443659+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MUTYH as Red List (low evidence)",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:05:15.433166+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mutyh has been classified as Red List (Low Evidence).",
"entity_name": "MUTYH",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:04:46.373319+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MUTYH: Rating: RED; 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": "2020-08-01T18:03:22.243013+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: MAX: Changed rating: RED",
"entity_name": "MAX",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:03:13.577378+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MAX as ready",
"entity_name": "MAX",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:03:13.566089+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: max has been classified as Green List (High Evidence).",
"entity_name": "MAX",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:03:09.338501+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MAX were changed from to {Pheochromocytoma, susceptibility to}, MIM# 171300",
"entity_name": "MAX",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:02:48.528995+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MAX were set to ",
"entity_name": "MAX",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:02:27.534856+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MAX was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MAX",
"entity_type": "gene"
},
{
"created": "2020-08-01T18:01:52.840676+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MAX: Rating: GREEN; Mode of pathogenicity: None; Publications: 21685915; Phenotypes: {Pheochromocytoma, susceptibility to}, MIM# 171300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MAX",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:59:23.955554+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HRAS as ready",
"entity_name": "HRAS",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:59:23.944690+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hras has been classified as Green List (High Evidence).",
"entity_name": "HRAS",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:58:57.474269+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HRAS were changed from to Costello syndrome, MIM# 218040",
"entity_name": "HRAS",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:58:40.152586+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HRAS was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HRAS",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:58:16.278624+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HRAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Costello syndrome, MIM# 218040; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HRAS",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:56:30.095341+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GATA2 as ready",
"entity_name": "GATA2",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:56:30.086943+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gata2 has been classified as Green List (High Evidence).",
"entity_name": "GATA2",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:56:26.567541+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GATA2 were changed from to {Leukemia, acute myeloid, susceptibility to}, MIM# 601626",
"entity_name": "GATA2",
"entity_type": "gene"
},
{
"created": "2020-08-01T17:56:00.785464+10:00",
"panel_name": "Cancer Predisposition_Paediatric",
"panel_id": 152,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GATA2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GATA2",
"entity_type": "gene"
}
]
}