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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=322",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=320",
"results": [
{
"created": "2024-12-13T15:57:46.719337+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WHRN were changed from Usher syndrome, type 2D, 611383 (3) to Usher syndrome, type 2D, MIM#611383",
"entity_name": "WHRN",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:57:19.201265+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.820",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WHRN were set to ",
"entity_name": "WHRN",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:56:56.925958+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.819",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: FERMT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26937547; Phenotypes: Kindler syndrome MIM#173650; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FERMT1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:56:53.287389+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYMK as ready",
"entity_name": "MYMK",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:56:53.275261+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mymk has been classified as Green List (High Evidence).",
"entity_name": "MYMK",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:56:49.927108+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYMK were changed from Carey-Fineman-Ziter syndrome, 254940 (3), Autosomal recessive to Carey-Fineman-Ziter syndrome, MIM#254940",
"entity_name": "MYMK",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:56:30.313268+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYMK were set to ",
"entity_name": "MYMK",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:55:59.568960+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED25 as ready",
"entity_name": "MED25",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:55:59.539254+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med25 has been classified as Green List (High Evidence).",
"entity_name": "MED25",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:55:56.127342+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MED25 were changed from Basel-Vanagait-Smirin-Yosef syndrome, 616449 (3) to Basel-Vanagait-Smirin-Yosef syndrome, MIM# 616449; congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome MONDO:0014643",
"entity_name": "MED25",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:55:41.454744+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MED25 were set to ",
"entity_name": "MED25",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:55:00.439260+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED17 as ready",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:55:00.401757+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med17 has been classified as Green List (High Evidence).",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:54:48.504059+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MED17 were changed from Microcephaly, postnatal progressive, with seizures and brain atrophy, 613668 (3) to Microcephaly, postnatal progressive, with seizures and brain atrophy, MIM#613668",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:54:32.058773+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.814",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MED17 were set to ",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:51:00.312029+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DOCK8 as ready",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:51:00.291517+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dock8 has been classified as Green List (High Evidence).",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:50:50.475883+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DOCK8 were changed from Hyper-IgE recurrent infection syndrome, autosomal recessive, 243700 (3) to Hyper-IgE recurrent infection syndrome, autosomal recessive, MIM#243700",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:50:34.647649+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.812",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DOCK8 were set to ",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:50:08.197170+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MANBA as ready",
"entity_name": "MANBA",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:50:08.183077+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: manba has been classified as Green List (High Evidence).",
"entity_name": "MANBA",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:50:03.833857+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MANBA were changed from Mannosidosis, beta, 248510 (3) to Mannosidosis, beta, MIM#248510",
"entity_name": "MANBA",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:49:37.650906+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.810",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: ZNHIT3: Rating: GREEN; Mode of pathogenicity: None; Publications: 39252897; Phenotypes: PEHO syndrome MIM#260565; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZNHIT3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:49:31.214814+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.810",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAI1 as ready",
"entity_name": "DNAI1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:49:31.204317+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.810",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnai1 has been classified as Green List (High Evidence).",
"entity_name": "DNAI1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:49:24.732811+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.810",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNAI1 were changed from Ciliary dyskinesia, primary, 1, with or without situs inversus, 244400 (3) to Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM#244400",
"entity_name": "DNAI1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:49:10.587303+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.809",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DNAI1 were set to ",
"entity_name": "DNAI1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:48:39.435898+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.808",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUSC3 as ready",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:48:39.424529+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.808",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tusc3 has been classified as Green List (High Evidence).",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:48:35.811891+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.808",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUSC3 were changed from Mental retardation, autosomal recessive 7, 611093 (3) to Intellectual developmental disorder, autosomal recessive 7 MIM#611093",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:48:21.515510+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.807",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUSC3 were set to ",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:47:36.651907+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAH11 as ready",
"entity_name": "DNAH11",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:47:36.636691+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnah11 has been classified as Green List (High Evidence).",
"entity_name": "DNAH11",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:47:32.622329+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNAH11 were changed from Ciliary dyskinesia, primary, 7, with or without situs inversus, 611884 (3) to Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884",
"entity_name": "DNAH11",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:47:17.364928+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DNAH11 were set to ",
"entity_name": "DNAH11",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:46:06.383999+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.804",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LYRM7 as ready",
"entity_name": "LYRM7",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:46:06.365064+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.804",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lyrm7 has been classified as Green List (High Evidence).",
"entity_name": "LYRM7",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:46:02.561235+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.804",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LYRM7 were changed from Mitochondrial complex III deficiency, nuclear type 8, 615838 (3), Autosomal recessive to Mitochondrial complex III deficiency, nuclear type 8, MIM#615838, Autosomal recessive",
"entity_name": "LYRM7",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:45:44.257867+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LYRM7 were set to ",
"entity_name": "LYRM7",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:44:37.097498+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLG3 as ready",
"entity_name": "DLG3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:44:37.069444+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlg3 has been classified as Green List (High Evidence).",
"entity_name": "DLG3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:44:32.847873+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DLG3 were changed from Mental retardation, X-linked 90, 300850 (3) to Intellectual developmental disorder, X-linked 90 MIM#300850",
"entity_name": "DLG3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:44:08.256308+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.801",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DLG3 were set to ",
"entity_name": "DLG3",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:43:06.757033+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBA8 as ready",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:43:06.740055+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tuba8 has been classified as Red List (Low Evidence).",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:42:56.527234+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBA8 were changed from Polymicrogyria with optic nerve hypoplasia, 613180 (3) to Polymicrogyria with optic nerve hypoplasia MONDO:0013172",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:42:42.814765+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.799",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: ZBTB24: Rating: GREEN; Mode of pathogenicity: None; Publications: 23486536; Phenotypes: Immunodeficiency-centromeric instability-facial anomalies syndrome 2, MIM# 614069, MONDO:0013553; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZBTB24",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:42:42.185382+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.799",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBA8 were set to ",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:41:07.465175+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LRPPRC as ready",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:41:07.454288+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lrpprc has been classified as Green List (High Evidence).",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:41:03.052792+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LRPPRC were changed from Leigh syndrome, French-Canadian type, 220111 (3) to Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian) MIM#220111",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:40:19.655861+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.797",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LRPPRC were set to ",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:36:55.543366+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.796",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: WNT10A: Rating: RED; Mode of pathogenicity: None; Publications: 19559398, 30426266; Phenotypes: Ectodermal dysplasia 16 (odontoonychodermal dysplasia) MIM#257980, Schopf-Schulz-Passarge syndrome MIM#224750, Tooth agenesis, selective, 4 MIM#150400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WNT10A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:34:42.826862+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.796",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDHD2 as ready",
"entity_name": "DDHD2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:34:42.812025+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.796",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddhd2 has been classified as Green List (High Evidence).",
"entity_name": "DDHD2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:34:38.236310+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.796",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDHD2 were changed from Spastic paraplegia 54, autosomal recessive, 615033 (3) to Spastic paraplegia 54, autosomal recessive, MIM#615033",
"entity_name": "DDHD2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:34:22.688230+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.795",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DDHD2 were set to ",
"entity_name": "DDHD2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:33:54.458969+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRDN as ready",
"entity_name": "TRDN",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:33:54.446831+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trdn has been classified as Green List (High Evidence).",
"entity_name": "TRDN",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:33:48.159303+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRDN were changed from Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness, 615441 (3) to Cardiac arrhythmia syndrome, with or without skeletal muscle weakness MIM#615441; Catecholaminergic polymorphic ventricular tachycardia MONDO:0017990",
"entity_name": "TRDN",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:33:33.064688+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.793",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRDN were set to ",
"entity_name": "TRDN",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:33:04.482852+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.792",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MARS2 as ready",
"entity_name": "MARS2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:33:04.457245+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.792",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mars2 has been classified as Green List (High Evidence).",
"entity_name": "MARS2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:33:00.672599+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.792",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MARS2 were changed from Spastic ataxia 3, autosomal recessive, 611390 (3) to Combined oxidative phosphorylation deficiency 25; MIM #616430, MONDO:0014636; Spastic ataxia 3, autosomal recessive, MIM #611390, MONDO:0012664",
"entity_name": "MARS2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:32:47.417753+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MARS2 were set to ",
"entity_name": "MARS2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:30:52.137925+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.790",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFSF11 as ready",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:30:52.100128+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.790",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfsf11 has been classified as Green List (High Evidence).",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:30:46.672151+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.790",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFSF11 were changed from Osteopetrosis, autosomal recessive 2, 259710 (3) to Osteopetrosis, autosomal recessive 2, MIM#259710",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:30:32.329543+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.789",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFSF11 were set to ",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:30:00.719120+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM70 as ready",
"entity_name": "TMEM70",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:30:00.698971+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem70 has been classified as Green List (High Evidence).",
"entity_name": "TMEM70",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:29:56.633453+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM70 were changed from Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, 614052 (3) to Mitochondrial disease MONDO:0044970",
"entity_name": "TMEM70",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:29:38.307348+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.787",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM70 were set to ",
"entity_name": "TMEM70",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:28:52.578603+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LINS1 as ready",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:28:52.566828+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lins1 has been classified as Green List (High Evidence).",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:28:41.425285+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LINS1 were changed from Mental retardation, autosomal recessive 27, 614340 (3) to Intellectual developmental disorder, autosomal recessive 2, MIM#614340",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:28:17.728009+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LINS1 were set to ",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:28:01.549718+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LINS1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:27:09.181227+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.784",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: VPS45: Rating: GREEN; Mode of pathogenicity: None; Publications: 30294941; Phenotypes: Neutropaenia, severe congenital, 5, autosomal recessive, MIM# 615285; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "VPS45",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:26:07.293685+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF1A as ready",
"entity_name": "KIF1A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:26:07.276821+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif1a has been classified as Green List (High Evidence).",
"entity_name": "KIF1A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:25:54.218752+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF1A were changed from Spastic paraplegia 30, autosomal recessive, 610357 (3) to Spastic paraplegia 30, autosomal recessive, MIM#610357",
"entity_name": "KIF1A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:25:41.563703+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF1A were set to ",
"entity_name": "KIF1A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:24:53.537795+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TIMM8A as ready",
"entity_name": "TIMM8A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:24:53.527136+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: timm8a has been classified as Green List (High Evidence).",
"entity_name": "TIMM8A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:24:45.180582+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TIMM8A were changed from Jensen syndrome, 311150 (3) to Mohr-Tranebjaerg syndrome MIM#304700",
"entity_name": "TIMM8A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:24:19.806771+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.781",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TIMM8A were set to ",
"entity_name": "TIMM8A",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:23:48.386919+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STXBP2 as ready",
"entity_name": "STXBP2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:23:48.369275+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stxbp2 has been classified as Green List (High Evidence).",
"entity_name": "STXBP2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:23:44.701072+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STXBP2 were changed from Hemophagocytic lymphohistiocytosis, familial, 5, 613101 (3) to Haemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease MIM#613101",
"entity_name": "STXBP2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:23:21.464621+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STXBP2 were set to ",
"entity_name": "STXBP2",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:22:54.299346+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LZTFL1 as ready",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:22:54.286168+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lztfl1 has been classified as Green List (High Evidence).",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:22:50.392146+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LZTFL1 were changed from Bardet-Biedl syndrome 17, 615994 (3) to Bardet-Biedl syndrome 17 MIM#615994; MONDO:0014445",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:22:37.359502+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LZTFL1 were set to ",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:22:08.423277+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SMS as ready",
"entity_name": "SMS",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:22:08.408065+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sms has been classified as Green List (High Evidence).",
"entity_name": "SMS",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:22:04.580039+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SMS were changed from Mental retardation, X-linked, Snyder-Robinson type, 309583 (3) to Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type MIM#309583",
"entity_name": "SMS",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:21:46.136478+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SMS were set to ",
"entity_name": "SMS",
"entity_type": "gene"
},
{
"created": "2024-12-13T15:21:18.928500+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.774",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: VARS2: Rating: GREEN; Mode of pathogenicity: None; Publications: 31064326; Phenotypes: Combined oxidative phosphorylation deficiency 20 MIM#615917; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "VARS2",
"entity_type": "gene"
}
]
}