HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1471",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1469",
"results": [
{
"created": "2020-12-20T13:31:44.240851+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.292",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PGAP3: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGAP3",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:31:29.694653+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.292",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PGAP3: Changed phenotypes: Hyperphosphatasia with mental retardation syndrome 4, MIM# 615716, MONDO:0014318",
"entity_name": "PGAP3",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:31:07.106953+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.292",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PGAP3: Changed rating: GREEN",
"entity_name": "PGAP3",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:31:00.436830+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.292",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PGAP3: Rating: ; Mode of pathogenicity: None; Publications: 24439110, 29620724, 30345601, 30217754; Phenotypes: Hyperphosphatasia with mental retardation syndrome 4, MIM# 615716; Mode of inheritance: None",
"entity_name": "PGAP3",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:26:58.917553+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGAP2 as ready",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:26:58.908935+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:26:54.198001+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PGAP2 as Amber List (moderate evidence)",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:26:54.189797+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:22:53.279619+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PGAP2 was added\ngene: PGAP2 was added to Genetic Epilepsy. Sources: Expert Review\nMode of inheritance for gene: PGAP2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PGAP2 were set to 23561846; 23561847; 31805394; 29119105; 27871432\nPhenotypes for gene: PGAP2 were set to Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207, MONDO:0013628\nReview for gene: PGAP2 was set to AMBER\nAdded comment: Bi-allelic variants in this gene are typically associated with severe DD/ID, hypotonia with very poor motor development, poor speech, and increased serum alkaline phosphatase, although presentations with milder ID have also been reported. More than 10 unrelated families reported.\r\n\r\nAlthough HPMRS disorders are frequently associated with seizures, this seems a less frequently reported feature associated with variants in this gene. \nSources: Expert Review",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:19:06.368935+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGAP2 as ready",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:19:06.360361+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap2 has been classified as Green List (High Evidence).",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:18:43.722217+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGAP2 were changed from to Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207, MONDO:0013628",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:18:13.564511+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3308",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGAP2 were set to ",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:17:39.439807+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PGAP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:17:04.316955+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PGAP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23561846, 23561847, 31805394, 29119105, 27871432; Phenotypes: Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207, MONDO:0013628; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:14:38.592095+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5715",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGAP2 as ready",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:14:38.580422+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5715",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap2 has been classified as Green List (High Evidence).",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:14:30.627039+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5715",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGAP2 were changed from to Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207, MONDO:0013628",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:14:10.550548+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGAP2 were set to ",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:13:51.063183+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5713",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PGAP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:13:30.968431+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PGAP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23561846, 23561847, 31805394, 29119105, 27871432; Phenotypes: Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207, MONDO:0013628; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:13:07.894141+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.292",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGAP2 were changed from Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207 to Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207, MONDO:0013628",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:12:31.356270+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.291",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PGAP2: Changed phenotypes: Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207, MONDO:0013628",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:11:39.803824+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.291",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGAP2 as ready",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:11:39.792546+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.291",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap2 has been classified as Green List (High Evidence).",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:11:37.094238+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.291",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGAP2 were changed from to Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:11:04.825933+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.290",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGAP2 were set to ",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:10:36.633574+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.289",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PGAP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-20T13:10:04.518898+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.288",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PGAP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23561846, 23561847, 31805394, 29119105, 27871432; Phenotypes: Hyperphosphatasia with mental retardation syndrome 3, MIM# 614207; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2020-12-19T22:00:51.315070+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGV as ready",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T22:00:51.303086+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigv has been classified as Green List (High Evidence).",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T22:00:46.428967+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIGV as Green List (high evidence)",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T22:00:46.421000+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigv has been classified as Green List (High Evidence).",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T22:00:15.884943+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.971",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PIGV was added\ngene: PIGV was added to Genetic Epilepsy. Sources: Expert Review\nMode of inheritance for gene: PIGV was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGV were set to 20802478; 22315194; 28817240; 24129430\nPhenotypes for gene: PIGV were set to Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300, MONDO:0009398\nReview for gene: PIGV was set to GREEN\nAdded comment: Bi-allelic variants in this gene are associated with intellectual disability, seizures, hypotonia, and hyperphosphatasia. Other features include facial dysmorphism, variable degrees of brachytelephalangy and congenital anomalies. \nSources: Expert Review",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:58:09.793738+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGV as ready",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:58:09.784040+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigv has been classified as Green List (High Evidence).",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:58:05.903985+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGV were changed from to Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300, MONDO:0009398",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:57:32.570771+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3305",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGV were set to ",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:57:01.845797+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3304",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGV was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:56:21.743377+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGV: Rating: GREEN; Mode of pathogenicity: None; Publications: 20802478, 22315194, 28817240, 24129430; Phenotypes: Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300, MONDO:0009398; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:55:36.653761+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGV as ready",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:55:36.640701+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigv has been classified as Green List (High Evidence).",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:55:28.307969+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGV were changed from to Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300, MONDO:0009398",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:54:32.548400+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGV were set to ",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:54:06.100913+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5710",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGV was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:53:45.174620+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGV: Rating: GREEN; Mode of pathogenicity: None; Publications: 20802478, 22315194, 28817240, 24129430; Phenotypes: Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300, MONDO:0009398; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:52:32.033456+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.288",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PIGV: Changed phenotypes: Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300, MONDO:0009398",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:52:21.490911+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.288",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGV as ready",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:52:21.482341+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.288",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigv has been classified as Green List (High Evidence).",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:52:17.646460+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.288",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGV were changed from Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300 to Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300, MONDO:0009398",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:51:30.195516+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.287",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGV were changed from to Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:51:08.149617+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.286",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGV were set to ",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:50:39.190096+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.285",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGV was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:50:07.741914+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.284",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGV: Rating: GREEN; Mode of pathogenicity: None; Publications: 20802478, 22315194, 28817240, 24129430; Phenotypes: Hyperphosphatasia with mental retardation syndrome 1, MIM# 239300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGV",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:45:00.524347+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGT were changed from Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398 to Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:44:22.671083+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PIGT: Changed phenotypes: Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:44:03.990802+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGT were changed from Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398 to Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:43:25.596318+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PIGT: Changed phenotypes: Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:37:09.039037+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGT were changed from Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398 to Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:36:42.512027+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PIGT: Changed phenotypes: Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:36:02.720487+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.284",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGT as ready",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:36:02.705328+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.284",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigt has been classified as Green List (High Evidence).",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:35:58.865726+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.284",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGT were changed from Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM#\t615398 to Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM#\t615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:28:00.459842+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGO as ready",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:28:00.451768+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigo has been classified as Green List (High Evidence).",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:26:13.759807+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGO were changed from to Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749, MONDO:0013882",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T21:25:50.910074+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGO were set to ",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:24:37.102646+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.967",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGO was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:23:46.378581+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGO: Rating: GREEN; Mode of pathogenicity: None; Publications: 22683086, 31698102, 28900819, 28545593, 28337824; Phenotypes: Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749, MONDO:0013882; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:22:59.749311+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGO as ready",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:22:59.738157+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigo has been classified as Green List (High Evidence).",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:22:54.991038+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGO were changed from to Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749, MONDO:0013882",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:22:21.030453+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3301",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGO were set to ",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:21:48.384158+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGO was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:21:14.593825+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3299",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGO: Rating: GREEN; Mode of pathogenicity: None; Publications: 22683086, 31698102, 28900819, 28545593, 28337824; Phenotypes: Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749, MONDO:0013882; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:20:29.661659+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGO as ready",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:20:29.652947+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigo has been classified as Green List (High Evidence).",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:20:21.308829+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGO were changed from to Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749, MONDO:0013882",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:20:01.139963+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5707",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGO were set to ",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:19:36.530910+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGO was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:19:18.986694+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGO: Rating: GREEN; Mode of pathogenicity: None; Publications: 22683086, 31698102, 28900819, 28545593, 28337824; Phenotypes: Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749, MONDO:0013882; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:18:55.303676+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.283",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGO were changed from Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749 to Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749, MONDO:0013882",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T20:18:21.007554+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.282",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PIGO: Changed phenotypes: Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749, MONDO:0013882",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:43:44.985580+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.282",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGO as ready",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:43:44.974015+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.282",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigo has been classified as Green List (High Evidence).",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:43:40.729130+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.282",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGO were changed from to Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:43:17.807269+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.281",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGO were set to ",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:42:50.809722+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.280",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGO was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:42:09.534440+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.279",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGO: Rating: GREEN; Mode of pathogenicity: None; Publications: 22683086, 31698102, 28900819, 28545593, 28337824; Phenotypes: Hyperphosphatasia with mental retardation syndrome 2, MIM# 614749; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGO",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:06:56.770546+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3299",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGN as ready",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:06:56.760333+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3299",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pign has been classified as Green List (High Evidence).",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:06:42.684771+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3299",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGN were changed from to Multiple congenital anomalies-hypotonia-seizures syndrome 1, MIM# 614080, MONDO:0013563",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:06:11.449274+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3298",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGN were set to ",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:05:39.761789+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3297",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PIGN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:05:07.056048+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3296",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGN: Rating: GREEN; Mode of pathogenicity: None; Publications: 21493957, 24253414, 26364997, 26394714, 33193741, 32585529, 29330547; Phenotypes: Multiple congenital anomalies-hypotonia-seizures syndrome 1, MIM# 614080, MONDO:0013563; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:04:12.372681+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: PIGN.\nTag founder tag was added to gene: PIGN.",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:03:49.787203+11:00",
"panel_name": "Congenital diaphragmatic hernia",
"panel_id": 69,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Three unrelated families reported with LOF variants and syndromic congenital diaphragmatic hernia, Fryns-like. Intragenic deletion is a common founder variant in La Reunion island.; to: Three unrelated families reported with LOF variants and syndromic congenital diaphragmatic hernia, Fryns-like. Intragenic deletion is a common founder variant in La Reunion island.",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:03:49.548850+11:00",
"panel_name": "Congenital diaphragmatic hernia",
"panel_id": 69,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Three unrelated families reported with LOF variants and syndromic congenital diaphragmatic hernia, Fryns-like.; to: Three unrelated families reported with LOF variants and syndromic congenital diaphragmatic hernia, Fryns-like. Intragenic deletion is a common founder variant in La Reunion island.",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:03:26.502072+11:00",
"panel_name": "Congenital diaphragmatic hernia",
"panel_id": 69,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: PIGN.\nTag founder tag was added to gene: PIGN.",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2020-12-19T19:03:06.322774+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGN as ready",
"entity_name": "PIGN",
"entity_type": "gene"
}
]
}