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[
{
"created": "2021-03-08T15:40:37.328536Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "1.6",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Added comment: Comment on phenotypes: This gene is also associated with Rhabdoid tumors, somatic (MIM# 609322); {Schwannomatosis-1, susceptibility to} (MIM# 162091); Coffin-Siris syndrome 3 (MIM# 614608)",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2021-03-08T15:40:37.308171Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "1.6",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Phenotypes for gene: SMARCB1 were changed from to {Rhabdoid tumor predisposition syndrome 1}, OMIM:609322; Rhabdoid tumor predisposition syndrome 1, MONDO:0012252",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2021-03-08T15:27:21.785216Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "1.5",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Added comment: Comment on phenotypes: This gene is also associated with Coffin-Siris syndrome 4 (MIM# 614609)",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2021-03-08T15:27:21.759695Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "1.5",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Phenotypes for gene: SMARCA4 were changed from to {Rhabdoid tumor predisposition syndrome 2}, OMIM:613325; Rhabdoid tumor predisposition syndrome 2, MONDO:0013224",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:55:01.545956Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "1.3",
"user_name": "Catherine Snow",
"item_type": "panel",
"text": "Panel version has been signed off",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-08-16T10:05:20.111568Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "1.0",
"user_name": "Ivone Leong",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-08-16T10:04:27.747303Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "0.9",
"user_name": "Ivone Leong",
"item_type": "panel",
"text": "Panel types changed to GMS Rare Disease; GMS signed-off",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-07-31T13:03:39.149279Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "0.8",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "commented on gene: SMARCB1",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2019-07-31T13:03:32.521626Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "0.8",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "commented on gene: SMARCA4",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2019-07-31T13:03:25.151758Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "0.8",
"user_name": "Ivone Leong",
"item_type": "panel",
"text": "List of related panels changed from to R358",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-01-30T16:10:30.875044Z",
"panel_name": "Rhabdoid tumour predisposition",
"panel_id": 600,
"panel_version": "0.7",
"user_name": "Ivone Leong",
"item_type": "panel",
"text": "Panel name changed from GMS - Familial rhabdoid tumours to Rhabdoid tumour predisposition",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-01-30T13:55:38.510260Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.6",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "Mode of inheritance for gene: SMARCB1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2019-01-30T13:55:13.444802Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.5",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "Mode of inheritance for gene: SMARCA4 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:21:34.940957Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.4",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "Classified gene: SMARCB1 as Green List (high evidence)",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:21:34.936124Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.4",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "Gene: smarcb1 has been classified as Green List (High Evidence).",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:21:24.611249Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.3",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "Classified gene: SMARCA4 as Green List (high evidence)",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:21:24.604764Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.3",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "Gene: smarca4 has been classified as Green List (High Evidence).",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:20:45.792446Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.2",
"user_name": "Rachel Robinson",
"item_type": "entity",
"text": "reviewed gene: SMARCA4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:20:45.781727Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.2",
"user_name": "Rachel Robinson",
"item_type": "entity",
"text": "reviewed gene: SMARCB1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:20:45.771668Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.2",
"user_name": "Lara Hawkes",
"item_type": "entity",
"text": "reviewed gene: SMARCA4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:20:45.762641Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.2",
"user_name": "Lara Hawkes",
"item_type": "entity",
"text": "reviewed gene: SMARCB1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:19:50.419748Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.1",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "gene: SMARCA4 was added\ngene: SMARCA4 was added to GMS - Familial rhabdoid tumours. Sources: Expert Review,NHS GMS\nMode of inheritance for gene: SMARCA4 was set to ",
"entity_name": "SMARCA4",
"entity_type": "gene"
},
{
"created": "2019-01-29T16:19:50.366196Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.1",
"user_name": "Ivone Leong",
"item_type": "entity",
"text": "gene: SMARCB1 was added\ngene: SMARCB1 was added to GMS - Familial rhabdoid tumours. Sources: Expert Review,NHS GMS\nMode of inheritance for gene: SMARCB1 was set to ",
"entity_name": "SMARCB1",
"entity_type": "gene"
},
{
"created": "2019-01-29T15:58:54.029420Z",
"panel_name": "GMS - Familial rhabdoid tumours",
"panel_id": 600,
"panel_version": "0.0",
"user_name": "Ivone Leong",
"item_type": "panel",
"text": "Added Panel GMS - Familial rhabdoid tumours\nSet panel types to: GMS Rare Disease",
"entity_name": null,
"entity_type": null
}
]