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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1911",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1909",
"results": [
{
"created": "2020-03-04T15:49:00.298938+11:00",
"panel_name": "Congenital Myasthenia",
"panel_id": 3078,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO9A as ready",
"entity_name": "MYO9A",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:49:00.285128+11:00",
"panel_name": "Congenital Myasthenia",
"panel_id": 3078,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo9a has been classified as Green List (High Evidence).",
"entity_name": "MYO9A",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:48:56.334521+11:00",
"panel_name": "Congenital Myasthenia",
"panel_id": 3078,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO9A were changed from congenital myasthenic syndrome 24, presynaptic 618198 to Congenital myasthenic syndrome 24, presynaptic 618198",
"entity_name": "MYO9A",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:48:42.940667+11:00",
"panel_name": "Congenital Myasthenia",
"panel_id": 3078,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO9A were set to ",
"entity_name": "MYO9A",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:47:04.863973+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SYNGAP1 as ready",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:47:04.855201+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: syngap1 has been classified as Green List (High Evidence).",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:47:01.439558+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SYNGAP1 were changed from to Intellectual disability, autosomal dominant 5, MIM # 612621",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:46:29.638109+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.626",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SYNGAP1 were set to ",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:46:05.338919+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.625",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SYNGAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:45:35.514343+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SYNGAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26079862; Phenotypes: Intellectual disability, autosomal dominant 5, MIM # 612621; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:43:29.688721+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SYNGAP1 as ready",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:43:29.679792+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: syngap1 has been classified as Green List (High Evidence).",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:43:21.214401+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SYNGAP1 were changed from to Intellectual disability, autosomal dominant 5 (MIM # 612621)",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:42:49.209434+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2376",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SYNGAP1 were set to ",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:42:20.598225+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2375",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SYNGAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:37:35.994644+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NBN as ready",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:37:35.985350+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbn has been classified as Amber List (Moderate Evidence).",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:37:29.324979+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NBN were changed from to Nijmegen breakage syndrome, MIM# 251260",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:37:01.383551+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2373",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NBN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:36:26.340557+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NBN as Amber List (moderate evidence)",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:36:26.328065+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbn has been classified as Amber List (Moderate Evidence).",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:35:43.346063+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NBN: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Nijmegen breakage syndrome, MIM# 251260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2020-03-04T15:24:46.916646+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2371",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: SYNGAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 26079862; Phenotypes: Intellectual disability, autosomal dominant 5 (MIM # 612621); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SYNGAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:54:29.424623+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-03-04T13:53:29.717208+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BEST1 as ready",
"entity_name": "BEST1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:53:29.708762+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: best1 has been classified as Green List (High Evidence).",
"entity_name": "BEST1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:52:47.461763+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-03-04T13:51:56.818026+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LOXL3 as ready",
"entity_name": "LOXL3",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:51:56.805082+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: loxl3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "LOXL3",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:51:37.039726+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL9A3 as ready",
"entity_name": "COL9A3",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:51:37.031107+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col9a3 has been classified as Green List (High Evidence).",
"entity_name": "COL9A3",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.895532+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: LOXL3 was added\ngene: LOXL3 was added to Stickler Syndrome. Sources: Expert list,Expert Review Amber\nMode of inheritance for gene: LOXL3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: LOXL3 were set to 30362103; 25663169\nPhenotypes for gene: LOXL3 were set to Stickler syndrome",
"entity_name": "LOXL3",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.829956+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: ZNF408 was added\ngene: ZNF408 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ZNF408 was set to Unknown",
"entity_name": "ZNF408",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.763030+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: VCAN was added\ngene: VCAN was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: VCAN was set to Unknown",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.695567+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: TSPAN12 was added\ngene: TSPAN12 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TSPAN12 was set to Unknown",
"entity_name": "TSPAN12",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.626986+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: NR2E3 was added\ngene: NR2E3 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NR2E3 was set to Unknown",
"entity_name": "NR2E3",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.557182+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: NDP was added\ngene: NDP was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NDP was set to Unknown",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.490550+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: LRP5 was added\ngene: LRP5 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LRP5 was set to Unknown",
"entity_name": "LRP5",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.424268+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: KIF11 was added\ngene: KIF11 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KIF11 was set to Unknown",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.357207+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: KCNJ13 was added\ngene: KCNJ13 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNJ13 was set to Unknown",
"entity_name": "KCNJ13",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.291283+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: GZF1 was added\ngene: GZF1 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GZF1 was set to Unknown",
"entity_name": "GZF1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.223672+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: FZD4 was added\ngene: FZD4 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FZD4 was set to Unknown",
"entity_name": "FZD4",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.154257+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: CTNNB1 was added\ngene: CTNNB1 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CTNNB1 was set to Unknown",
"entity_name": "CTNNB1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.087676+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: COL9A3 was added\ngene: COL9A3 was added to Stickler Syndrome. Sources: Expert Review Green,Other\nMode of inheritance for gene: COL9A3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: COL9A3 were set to 31090205; 30450842; 20301479; 24273071\nPhenotypes for gene: COL9A3 were set to sensorineural hearing loss; midface hypoplasia; Stickler syndrome; myopia",
"entity_name": "COL9A3",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:41.021138+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: COL9A2 was added\ngene: COL9A2 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL9A2 was set to Unknown",
"entity_name": "COL9A2",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:40.954719+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: COL9A1 was added\ngene: COL9A1 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL9A1 was set to Unknown",
"entity_name": "COL9A1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:40.888037+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: COL2A1 was added\ngene: COL2A1 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL2A1 was set to Unknown",
"entity_name": "COL2A1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:40.822879+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: COL18A1 was added\ngene: COL18A1 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL18A1 was set to Unknown",
"entity_name": "COL18A1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:40.757255+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: COL11A2 was added\ngene: COL11A2 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL11A2 was set to Unknown",
"entity_name": "COL11A2",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:40.675820+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: COL11A1 was added\ngene: COL11A1 was added to Stickler Syndrome. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL11A1 was set to Unknown",
"entity_name": "COL11A1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:40.605343+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: CAPN5 was added\ngene: CAPN5 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CAPN5 was set to Unknown",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:40.539136+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: BEST1 was added\ngene: BEST1 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BEST1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: BEST1 were set to Vitreoretinochoroidopathy, MIM# 193220",
"entity_name": "BEST1",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:40.473189+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "gene: ATOH7 was added\ngene: ATOH7 was added to Vitreoretinopathy. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ATOH7 was set to Unknown",
"entity_name": "ATOH7",
"entity_type": "gene"
},
{
"created": "2020-03-04T13:45:21.022482+11:00",
"panel_name": "Stickler Syndrome",
"panel_id": 3114,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "panel",
"text": "Added panel Stickler Syndrome",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-03-04T13:45:21.010035+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.0",
"user_name": "Alison Yeung",
"item_type": "panel",
"text": "Added panel Vitreoretinopathy",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-03-04T12:31:47.602473+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZDHHC15 as ready",
"entity_name": "ZDHHC15",
"entity_type": "gene"
},
{
"created": "2020-03-04T12:31:47.586681+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zdhhc15 has been classified as Red List (Low Evidence).",
"entity_name": "ZDHHC15",
"entity_type": "gene"
},
{
"created": "2020-03-04T12:31:32.847076+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZDHHC15 were changed from to Mental retardation, X-linked 91, 300577",
"entity_name": "ZDHHC15",
"entity_type": "gene"
},
{
"created": "2020-03-04T12:31:18.584260+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1623",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZDHHC15 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "ZDHHC15",
"entity_type": "gene"
},
{
"created": "2020-03-04T12:31:06.045385+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZDHHC15 as Red List (low evidence)",
"entity_name": "ZDHHC15",
"entity_type": "gene"
},
{
"created": "2020-03-04T12:31:06.031741+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zdhhc15 has been classified as Red List (Low Evidence).",
"entity_name": "ZDHHC15",
"entity_type": "gene"
},
{
"created": "2020-03-04T12:30:44.247668+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1621",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZDHHC15: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, X-linked 91, 300577; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "ZDHHC15",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:33:07.106353+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZBTB24 as ready",
"entity_name": "ZBTB24",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:33:07.092553+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb24 has been classified as Green List (High Evidence).",
"entity_name": "ZBTB24",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:33:00.016208+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZBTB24 were changed from to Immunodeficiency-centromeric instability-facial anomalies syndrome 2; OMIM # 614069",
"entity_name": "ZBTB24",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:32:32.577571+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2370",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZBTB24 were set to ",
"entity_name": "ZBTB24",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:32:02.923564+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2369",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZBTB24 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZBTB24",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:24:27.875465+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1621",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZBTB16 as ready",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:24:27.867120+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1621",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:23:59.510669+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1621",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZBTB16 were changed from to Skeletal defects, genital hypoplasia, and mental retardation, OMIM #612447",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:23:45.313728+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1620",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZBTB16 were set to ",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:23:30.800503+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1619",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZBTB16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:23:13.746358+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZBTB16 as Amber List (moderate evidence)",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:23:13.737584+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:22:52.410702+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZBTB16: Rating: AMBER; Mode of pathogenicity: None; Publications: 18611983; Phenotypes: Skeletal defects, genital hypoplasia, and mental retardation, OMIM #612447; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:22:06.814316+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2368",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZBTB16 as ready",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:22:06.805224+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2368",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:22:01.744257+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2368",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZBTB16 were changed from to Skeletal defects, genital hypoplasia, and mental retardation, OMIM #612447",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:21:34.377572+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2367",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZBTB16 were set to ",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:21:04.712946+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZBTB16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:19:12.363414+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZBTB11 as ready",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:19:12.350042+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:19:04.643977+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZBTB11 were changed from to Intellectual developmental disorder, autosomal recessive 69, OMIM #618383",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:18:42.298984+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZBTB11 were set to ",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:18:29.125572+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1615",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZBTB11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:18:03.488888+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZBTB11 as Amber List (moderate evidence)",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:18:03.480162+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:17:39.233773+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZBTB11: Rating: AMBER; Mode of pathogenicity: None; Publications: 29893856; Phenotypes: Intellectual developmental disorder, autosomal recessive 69, OMIM #618383; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:16:51.547314+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2365",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZBTB11 as ready",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:16:51.532505+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2365",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:16:43.646353+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2365",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZBTB11 were changed from to Intellectual developmental disorder, autosomal recessive 69; OMIM #618383",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:16:11.166829+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2364",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZBTB11 were set to ",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:15:38.630743+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZBTB11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZBTB11",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:13:51.393728+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: YAP1 were set to ",
"entity_name": "YAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:13:17.452124+11:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: YAP1: Added comment: Four families reported; incomplete penetrance and variable expressivity.; Changed publications: 24462371, 27267789, 28801591",
"entity_name": "YAP1",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:04:36.465996+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XPA were set to ",
"entity_name": "XPA",
"entity_type": "gene"
},
{
"created": "2020-03-04T11:03:53.033047+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2361",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: XPA: Rating: GREEN; Mode of pathogenicity: None; Publications: 26302748, 25566891, 24135642; Phenotypes: Xeroderma pigmentosum, group A, OMIM# 278700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPA",
"entity_type": "gene"
},
{
"created": "2020-03-04T10:49:20.486723+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2361",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WNT5A: Rating: GREEN; Mode of pathogenicity: None; Publications: 17256787; Phenotypes: Robinow syndrome, autosomal dominant 1, OMIM# 180700; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2020-03-04T10:44:16.258623+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNT3 as ready",
"entity_name": "WNT3",
"entity_type": "gene"
},
{
"created": "2020-03-04T10:44:16.249078+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt3 has been classified as Red List (Low Evidence).",
"entity_name": "WNT3",
"entity_type": "gene"
}
]
}