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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1727",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1725",
"results": [
{
"created": "2020-07-16T18:10:19.673498+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DEAF1 were set to ",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T18:09:56.577895+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DEAF1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T18:09:30.524687+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DEAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 30923367, 24726472, 26048982, 28940898, 26834045; Phenotypes: Neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures 617171, Vulto-van Silfout-de Vries syndrome 615828; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T18:06:28.052610+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DEAF1 as ready",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T18:06:28.044221+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: deaf1 has been classified as Green List (High Evidence).",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T18:06:21.388310+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DEAF1 were changed from to Neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures 617171; Vulto-van Silfout-de Vries syndrome 615828",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T18:06:00.295567+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DEAF1 were set to ",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T18:05:39.059402+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3370",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: DEAF1 was changed from to Other",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T18:05:24.481775+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3369",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DEAF1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:39:26.867258+10:00",
"panel_name": "Multiple pterygium syndrome",
"panel_id": 139,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RIPK4 as ready",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:39:26.855976+10:00",
"panel_name": "Multiple pterygium syndrome",
"panel_id": 139,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ripk4 has been classified as Green List (High Evidence).",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:39:05.921416+10:00",
"panel_name": "Multiple pterygium syndrome",
"panel_id": 139,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RIPK4 as Green List (high evidence)",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:39:05.914198+10:00",
"panel_name": "Multiple pterygium syndrome",
"panel_id": 139,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ripk4 has been classified as Green List (High Evidence).",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:38:43.215336+10:00",
"panel_name": "Multiple pterygium syndrome",
"panel_id": 139,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RIPK4 was added\ngene: RIPK4 was added to Multiple pterygium syndrome. Sources: Expert Review\nMode of inheritance for gene: RIPK4 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RIPK4 were set to 28940926; 22197489; 22197488\nPhenotypes for gene: RIPK4 were set to Popliteal pterygium syndrome, Bartsocas-Papas type, MIM# 263650\nReview for gene: RIPK4 was set to GREEN\nAdded comment: At least three unrelated families reported. \nSources: Expert Review",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:37:26.454305+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RIPK4 as ready",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:37:26.446736+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ripk4 has been classified as Green List (High Evidence).",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:37:24.222839+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RIPK4 were changed from to Popliteal pterygium syndrome, Bartsocas-Papas type, MIM# 263650",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:37:00.830803+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RIPK4 were set to ",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:36:45.235681+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RIPK4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T17:36:22.715604+10:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RIPK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 28940926, 22197489, 22197488; Phenotypes: Popliteal pterygium syndrome, Bartsocas-Papas type, MIM# 263650; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RIPK4",
"entity_type": "gene"
},
{
"created": "2020-07-16T16:49:49.819291+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3368",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "reviewed gene: SMC3: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 18996922, 25655089, 31334757; Phenotypes: ornelia de Lange syndrome 3, 610759; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "SMC3",
"entity_type": "gene"
},
{
"created": "2020-07-16T16:47:46.554460+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3368",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "reviewed gene: DEAF1: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID 30923367, PMID 24726472; Phenotypes: Neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures 617171, Vulto-van Silfout-de Vries syndrome 615828; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "DEAF1",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:14:51.918345+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GRM7 were changed from Epilepsy, microcephaly, developmental delay to Epilepsy, microcephaly, developmental delay; neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities (NEDSHBA), MIM#618922",
"entity_name": "GRM7",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:11:54.276134+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GRM7 were changed from Epilepsy, microcephaly, developmental delay to Epilepsy, microcephaly, developmental delay; neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities (NEDSHBA), MIM#618922",
"entity_name": "GRM7",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:11:29.564608+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: GRM7: Changed phenotypes: Epilepsy, microcephaly, developmental delay, neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities (NEDSHBA), MIM#618922",
"entity_name": "GRM7",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:10:56.781950+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3368",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GRM7 were changed from Epilepsy, microcephaly, developmental delay to Epilepsy, microcephaly, developmental delay; neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities (NEDSHBA), MIM#618922",
"entity_name": "GRM7",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:10:40.585007+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3367",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: GRM7: Changed phenotypes: Epilepsy, microcephaly, developmental delay, neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities (NEDSHBA), MIM#618922",
"entity_name": "GRM7",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:10:22.410597+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GRM7 were changed from Epilepsy, microcephaly, developmental delay to Epilepsy, microcephaly, developmental delay; neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities (NEDSHBA), MIM#618922",
"entity_name": "GRM7",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:09:52.314348+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: GRM7: Changed phenotypes: Epilepsy, microcephaly, developmental delay, neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities (NEDSHBA), MIM#618922",
"entity_name": "GRM7",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:08:27.824269+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3367",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLCC1 were changed from Retinitis pigmentosa 32 to Retinitis pigmentosa 32, MIM# 609913",
"entity_name": "CLCC1",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:08:04.116836+10:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa",
"panel_id": 277,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLCC1 were changed from Retinitis pigmentosa 32 to Retinitis pigmentosa 32, MIM# 609913",
"entity_name": "CLCC1",
"entity_type": "gene"
},
{
"created": "2020-07-16T09:07:45.105480+10:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa",
"panel_id": 277,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CLCC1: Rating: AMBER; Mode of pathogenicity: None; Publications: 30157172; Phenotypes: Retinitis pigmentosa 32, MIM# 609913; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CLCC1",
"entity_type": "gene"
},
{
"created": "2020-07-15T22:02:32.544917+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ABCC9 as ready",
"entity_name": "ABCC9",
"entity_type": "gene"
},
{
"created": "2020-07-15T22:02:32.538536+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: abcc9 has been classified as Green List (High Evidence).",
"entity_name": "ABCC9",
"entity_type": "gene"
},
{
"created": "2020-07-15T22:02:26.808988+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ABCC9 were changed from to Hypertrichotic osteochondrodysplasia, MIM# 239850; Cantu syndrome; mild ID, similar facies, myopathy, cerebral white matter hyperintensities; cardiac systolic dysfunction",
"entity_name": "ABCC9",
"entity_type": "gene"
},
{
"created": "2020-07-15T22:02:09.785605+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3365",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ABCC9 were set to ",
"entity_name": "ABCC9",
"entity_type": "gene"
},
{
"created": "2020-07-15T22:01:53.950224+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3364",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ABCC9 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ABCC9",
"entity_type": "gene"
},
{
"created": "2020-07-15T22:01:37.634971+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ABCC9: Rating: GREEN; Mode of pathogenicity: Other; Publications: 31575858, 22610116, 22608503; Phenotypes: Hypertrichotic osteochondrodysplasia, MIM# 239850, Cantu syndrome, mild ID, similar facies, myopathy, cerebral white matter hyperintensities, cardiac systolic dysfunction; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ABCC9",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:45:42.375550+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-07-15T18:44:50.432330+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-07-15T18:43:54.562042+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSPYL1 as ready",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:43:54.554673+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tspyl1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:43:48.605987+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSPYL1 were changed from to Sudden infant death with dysgenesis of the testes syndrome (MIM#608800)",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:43:32.964806+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSPYL1 were set to ",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:43:17.230128+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3361",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSPYL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:43:01.912908+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3360",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSPYL1 as Amber List (moderate evidence)",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:43:01.904667+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3360",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tspyl1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:42:47.833898+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: TSPYL1.",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:42:37.736417+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3359",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSPYL1: Rating: AMBER; Mode of pathogenicity: None; Publications: 15273283, 19463995, 22137496, 25449952, 16418600; Phenotypes: Sudden infant death with dysgenesis of the testes syndrome (MIM#608800); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:41:29.490464+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSPYL1 as Amber List (moderate evidence)",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:41:29.483978+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tspyl1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:40:46.107873+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSPYL1 as ready",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:40:46.095999+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tspyl1 has been classified as Red List (Low Evidence).",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:40:43.183295+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSPYL1 were changed from to Sudden infant death with dysgenesis of the testes syndrome (MIM#608800)",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:40:18.232042+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSPYL1 were set to ",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:39:57.691326+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSPYL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:39:36.921417+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSPYL1 as Red List (low evidence)",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:39:36.914132+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tspyl1 has been classified as Red List (Low Evidence).",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:38:20.359533+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR11 as ready",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:38:20.351968+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr11 has been classified as Green List (High Evidence).",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:38:17.625393+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR11 were changed from to Hypogonadotropic hypogonadism 14 with or without anosmia, MIM#614858",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:37:55.736290+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR11 were set to ",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:37:30.700236+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:32:49.936135+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KISS1R as ready",
"entity_name": "KISS1R",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:32:49.925999+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kiss1r has been classified as Green List (High Evidence).",
"entity_name": "KISS1R",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:32:46.940522+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KISS1R were changed from to Hypogonadotropic hypogonadism 8 with or without anosmia (MIM#614837)",
"entity_name": "KISS1R",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:32:25.436164+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KISS1R were set to ",
"entity_name": "KISS1R",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:32:03.600624+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KISS1R was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KISS1R",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:12:51.666885+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGM were changed from portal vein thrombosis; persistent absence seizures; macrocephaly; infantile-onset cerebrovascular thrombotic events; portal vein thrombosis; persistent absence seizures; macrocephaly; infantile-onset cerebrovascular thrombotic events to portal vein thrombosis; persistent absence seizures; macrocephaly; infantile-onset cerebrovascular thrombotic events; portal vein thrombosis; persistent absence seizures; macrocephaly; infantile-onset cerebrovascular thrombotic events",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:12:38.061998+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGM were changed from portal vein thrombosis; persistent absence seizures; macrocephaly; infantile-onset cerebrovascular thrombotic events to portal vein thrombosis; persistent absence seizures; macrocephaly; infantile-onset cerebrovascular thrombotic events; portal vein thrombosis; persistent absence seizures; macrocephaly; infantile-onset cerebrovascular thrombotic events",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:12:24.966955+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3359",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGM as ready",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:12:24.956383+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3359",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigm has been classified as Amber List (Moderate Evidence).",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:12:11.730672+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3359",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGM were changed from to Glycosylphosphatidylinositol deficiency, MIM#\t610293; portal vein thrombosis; persistent absence seizures; macrocephaly; infantile-onset cerebrovascular thrombotic events",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:11:33.811414+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3358",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGM were set to ",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:11:18.771068+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3357",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:11:07.414949+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3356",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIGM as Amber List (moderate evidence)",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:11:07.404733+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3356",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigm has been classified as Amber List (Moderate Evidence).",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:10:53.033793+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: PIGM.",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:06:31.336194+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LEP as ready",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:06:31.323842+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lep has been classified as Green List (High Evidence).",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:06:18.160974+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LEP as ready",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:06:18.152663+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lep has been classified as Green List (High Evidence).",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:06:12.155608+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LEP were changed from to Obesity, morbid, due to leptin deficiency (MIM#614962)",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:05:56.221185+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3354",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LEP were set to ",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:05:40.928738+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LEP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:05:15.770031+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LEP were changed from Obesity, morbid, due to leptin deficiency (MIM#614962) to Obesity, morbid, due to leptin deficiency (MIM#614962)",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:05:06.718602+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ST3GAL3 as ready",
"entity_name": "ST3GAL3",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:05:06.711041+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: st3gal3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ST3GAL3",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:04:59.922263+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LEP were changed from to Obesity, morbid, due to leptin deficiency (MIM#614962)",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:04:37.193336+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LEP were set to ",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:04:15.679714+10:00",
"panel_name": "Disorders of Sex Differentiation",
"panel_id": 99,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LEP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LEP",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:01:10.213107+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUS1 as ready",
"entity_name": "NUS1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:01:10.202107+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nus1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NUS1",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:01:07.075037+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ST3GAL3 were changed from to Mental retardation, autosomal recessive 12 MIM# 611090",
"entity_name": "ST3GAL3",
"entity_type": "gene"
},
{
"created": "2020-07-15T18:00:53.501165+10:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NUS1 were set to ",
"entity_name": "NUS1",
"entity_type": "gene"
},
{
"created": "2020-07-15T17:54:34.369657+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3352",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LEPR as ready",
"entity_name": "LEPR",
"entity_type": "gene"
},
{
"created": "2020-07-15T17:54:34.363002+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3352",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lepr has been classified as Green List (High Evidence).",
"entity_name": "LEPR",
"entity_type": "gene"
},
{
"created": "2020-07-15T17:54:27.952965+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3352",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LEPR were changed from to Obesity, morbid, due to leptin receptor deficiency (MIM#614963)",
"entity_name": "LEPR",
"entity_type": "gene"
},
{
"created": "2020-07-15T17:54:12.679631+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3351",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LEPR were set to ",
"entity_name": "LEPR",
"entity_type": "gene"
},
{
"created": "2020-07-15T17:53:55.009716+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LEPR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LEPR",
"entity_type": "gene"
}
]
}