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{
"count": 220314,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1340",
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"results": [
{
"created": "2021-04-24T18:53:52.961557+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7335",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TGIF1 as ready",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:53:52.948314+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7335",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tgif1 has been classified as Green List (High Evidence).",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:53:44.783319+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7335",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TGIF1 were changed from to Holoprosencephaly 4, MIM# 142946; MONDO:0007734",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:53:16.357652+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7334",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TGIF1 were set to ",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:52:42.267908+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7333",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TGIF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:52:22.761039+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7332",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TGIF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10835638, 16323008; Phenotypes: Holoprosencephaly 4, MIM# 142946, MONDO:0007734; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:51:22.183457+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TGIF1 as ready",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:51:22.171796+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tgif1 has been classified as Green List (High Evidence).",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:51:19.059057+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TGIF1 were changed from to Holoprosencephaly 4, MIM# 142946; MONDO:0007734",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:50:50.649997+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TGIF1 were set to ",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:50:27.521969+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TGIF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:49:55.566102+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TGIF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10835638, 16323008; Phenotypes: Holoprosencephaly 4, MIM# 142946, MONDO:0007734; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TGIF1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:23:46.040264+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7332",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SIX3 as ready",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:23:46.030103+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7332",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: six3 has been classified as Green List (High Evidence).",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:23:39.053744+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7332",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SIX3 were changed from to Holoprosencephaly 2, MIM# 157170; MONDO:0007999",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:23:20.005170+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7331",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SIX3 were set to ",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:23:04.456392+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7330",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SIX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:22:46.335365+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7329",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SIX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 10369266, 16323008, 19346217; Phenotypes: Holoprosencephaly 2, MIM# 157170, MONDO:0007999; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:22:19.518555+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SIX3 as ready",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:22:19.507508+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: six3 has been classified as Green List (High Evidence).",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:22:12.384502+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SIX3 were changed from to Holoprosencephaly 2, MIM# 157170; MONDO:0007999",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:21:40.863599+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SIX3 were set to ",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:21:13.490247+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SIX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:20:23.758537+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SIX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 10369266, 16323008, 19346217; Phenotypes: Holoprosencephaly 2, MIM# 157170, MONDO:0007999; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:16:17.892128+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTCH1 as ready",
"entity_name": "PTCH1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:16:17.880261+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptch1 has been classified as Green List (High Evidence).",
"entity_name": "PTCH1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:16:14.621786+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTCH1 were changed from to Holoprosencephaly 7, MIM# 610828",
"entity_name": "PTCH1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:15:47.137189+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PTCH1 were set to ",
"entity_name": "PTCH1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:15:18.589306+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PTCH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTCH1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:14:45.759082+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PTCH1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11941477, 17001668, 29575684; Phenotypes: Holoprosencephaly 7, MIM# 610828; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTCH1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:11:50.216632+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GLI2 as ready",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:11:50.207180+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gli2 has been classified as Green List (High Evidence).",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:11:46.778977+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GLI2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:11:29.380657+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GLI2 were set to ",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:10:57.132758+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GLI2 were changed from to Holoprosencephaly 9, MIM# 610829; MONDO:0012563",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:10:09.102992+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GLI2: Rating: GREEN; Mode of pathogenicity: None; Publications: 14581620, 17096318, 33235745, 27585885; Phenotypes: Holoprosencephaly 9, MIM# 610829; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:07:09.640466+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGFR1 as ready",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:07:09.631529+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgfr1 has been classified as Green List (High Evidence).",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:07:06.263374+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGFR1 were changed from to Hartsfield syndrome, MIM# 615465",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:06:38.259805+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FGFR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:06:14.425546+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FGFR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hartsfield syndrome, MIM# 615465; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGFR1",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:05:11.673084+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGF8 as ready",
"entity_name": "FGF8",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:05:11.661493+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgf8 has been classified as Green List (High Evidence).",
"entity_name": "FGF8",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:05:09.058187+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGF8 were changed from to Holoprosencephaly; MONDO:0016296",
"entity_name": "FGF8",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:04:46.334795+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FGF8 were set to ",
"entity_name": "FGF8",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:04:08.931770+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FGF8 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGF8",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:03:39.188998+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: FGF8: Changed phenotypes: Holoprosencephaly, MONDO:0016296",
"entity_name": "FGF8",
"entity_type": "gene"
},
{
"created": "2021-04-24T18:02:40.739168+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FGF8: Rating: GREEN; Mode of pathogenicity: None; Publications: 27363716, 29584859; Phenotypes: Holoprosencephaly; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGF8",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:59:51.788024+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DISP1 as ready",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:59:51.770439+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: disp1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:59:46.408236+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7329",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DISP1 as ready",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:59:46.399264+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7329",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: disp1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:59:38.663159+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7329",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DISP1 were changed from to Holoprosencephaly",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:59:20.319183+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7328",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DISP1 were set to ",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:59:01.852171+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7327",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DISP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:58:45.363648+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7326",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DISP1 as Amber List (moderate evidence)",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:58:45.352909+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7326",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: disp1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:58:28.142614+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7325",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DISP1: Rating: AMBER; Mode of pathogenicity: None; Publications: 19184110, 26748417, 23542665; Phenotypes: Holoprosencephaly; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:58:27.041298+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DISP1 were changed from to Holoprosencephaly",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:57:58.153707+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DISP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:57:24.188755+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: DISP1 was changed from to Other",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:56:34.833865+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DISP1 were set to ",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:56:08.736713+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DISP1 as Amber List (moderate evidence)",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:56:08.726178+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: disp1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T17:55:35.375834+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DISP1: Rating: AMBER; Mode of pathogenicity: Other; Publications: 19184110, 26748417, 23542665; Phenotypes: Holoprosencephaly; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2021-04-24T15:03:10.202514+10:00",
"panel_name": "Anophthalmia_Microphthalmia_Coloboma",
"panel_id": 42,
"panel_version": "1.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CDON were changed from Holoprosencephaly 11\tMIM#614226 to Coloboma",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T15:01:44.539477+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDON as ready",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T15:01:44.528020+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdon has been classified as Green List (High Evidence).",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T15:01:41.845812+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CDON were changed from to Holoprosencephaly 11, MIM# 614226; MONDO:0013642",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T15:01:19.186769+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CDON were set to ",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T15:00:49.268492+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CDON was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T15:00:22.672937+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: CDON: Changed phenotypes: Holoprosencephaly 11, MIM# 614226, MONDO:0013642",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T15:00:02.660604+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: >5 unrelated families reported, however note some of the variants are present at a very low frequenting in gnomad (1-4) and some are inherited. Mouse model.; to: >5 unrelated families reported, however note some of the variants are present at a very low frequentcy in gnomad (1-4) and some are inherited. Mouse model.",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:59:52.554330+10:00",
"panel_name": "Holoprosencephaly and septo-optic dysplasia",
"panel_id": 112,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CDON: Rating: GREEN; Mode of pathogenicity: None; Publications: 21802063, 26529631, 26728615, 23071453; Phenotypes: Holoprosencephaly 11, MIM# 614226; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:48:52.787534+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2021-04-24T14:48:23.923427+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGFR2 as ready",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:48:23.913098+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgfr2 has been classified as Green List (High Evidence).",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:48:20.404133+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FGFR2 as Green List (high evidence)",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:48:20.394252+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgfr2 has been classified as Green List (High Evidence).",
"entity_name": "FGFR2",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:46:31.793859+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBX3 as ready",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:46:31.783467+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbx3 has been classified as Green List (High Evidence).",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:46:24.325643+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBX3 were changed from to Ulnar-mammary syndrome, MIM# 181450; MONDO:0008411",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:46:00.760336+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBX3 were set to ",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:45:31.430229+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:44:56.588486+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7325",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBX3 as ready",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:44:56.578605+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7325",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbx3 has been classified as Green List (High Evidence).",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:44:48.027708+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7325",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBX3 were changed from to Ulnar-mammary syndrome, MIM# 181450; MONDO:0008411",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:44:28.987698+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7324",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBX3 were set to ",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:44:10.586132+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7323",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:43:53.225230+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7322",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 9207801, 19938096, 28145909; Phenotypes: Ulnar-mammary syndrome, MIM# 181450, MONDO:0008411; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:43:05.400685+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 9207801, 19938096, 28145909; Phenotypes: Ulnar-mammary syndrome, MIM# 181450, MONDO:0008411; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:40:13.820770+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLX4 as ready",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:40:13.810218+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slx4 has been classified as Green List (High Evidence).",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:40:10.564191+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLX4 were changed from to Fanconi anaemia, complementation group P, MIM# 613951; MONDO:0013499",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:39:46.488900+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLX4 were set to ",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:39:17.507288+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLX4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:38:46.406803+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SLX4: Changed phenotypes: Fanconi anaemia, complementation group P, MIM# 613951, MONDO:0013499",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:38:26.895574+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SLX4: Changed phenotypes: Fanconi anaemia, complementation group P, MIM# 613951",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:37:55.713415+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SALL4 as ready",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:37:55.703470+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sall4 has been classified as Green List (High Evidence).",
"entity_name": "SALL4",
"entity_type": "gene"
}
]
}