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{
"count": 220828,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=727",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=725",
"results": [
{
"created": "2022-10-06T13:49:44.229464+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOG as ready",
"entity_name": "NOG",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:49:44.220404+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nog has been classified as Red List (Low Evidence).",
"entity_name": "NOG",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:49:40.516193+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NOG were changed from Symphalangism, proximal, 1A to Brachydactyly, type B2 - MIM#611377; Multiple synostoses syndrome 1 (MIM#186500); Stapes ankylosis with broad thumbs and toes (MIM#184460); Symphalangism, proximal, 1A (MIM#185800); Tarsal-carpal coalition syndrome (MIM#186570)",
"entity_name": "NOG",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:49:28.766215+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NOG as Red List (low evidence)",
"entity_name": "NOG",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:49:28.758394+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nog has been classified as Red List (Low Evidence).",
"entity_name": "NOG",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:49:17.435391+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: NOG: Changed rating: RED",
"entity_name": "NOG",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:49:09.710817+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NOG: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Brachydactyly, type B2 - MIM#611377, Multiple synostoses syndrome 1 (MIM#186500), Stapes ankylosis with broad thumbs and toes (MIM#184460), Symphalangism, proximal, 1A (MIM#185800), Tarsal-carpal coalition syndrome (MIM#186570); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NOG",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:48:16.664016+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NNT as ready",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:48:16.654817+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nnt has been classified as Green List (High Evidence).",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:48:12.698810+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NNT were set to ",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:48:01.728356+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: NNT.",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:47:53.268008+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NNT: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Glucocorticoid deficiency 4, with or without mineralocorticoid deficiency - MIM#614736; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:47:15.403624+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NKX2-1 as ready",
"entity_name": "NKX2-1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:47:15.395514+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nkx2-1 has been classified as Green List (High Evidence).",
"entity_name": "NKX2-1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:47:12.223841+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NKX2-1 were changed from Choreoathetosis, hypothyroidism, and neonatal respiratory distress to Choreoathetosis, hypothyroidism, and neonatal respiratory distress MIM#610978",
"entity_name": "NKX2-1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:47:07.363505+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.442",
"user_name": "David Amor",
"item_type": "entity",
"text": "reviewed gene: OPA1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Optic atrophy 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "OPA1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:46:55.935077+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NKX2-1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Choreoathetosis, hypothyroidism, and neonatal respiratory distress MIM#610978; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NKX2-1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:46:04.540876+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NIPBL as ready",
"entity_name": "NIPBL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:46:04.532015+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nipbl has been classified as Red List (Low Evidence).",
"entity_name": "NIPBL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:46:00.718163+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NIPBL were changed from Cornelia de Lange syndrome to Cornelia de Lange syndrome 1, MIM# 122470",
"entity_name": "NIPBL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:45:46.630996+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NIPBL as Red List (low evidence)",
"entity_name": "NIPBL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:45:46.621759+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nipbl has been classified as Red List (Low Evidence).",
"entity_name": "NIPBL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:45:29.910171+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NIPBL: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cornelia de Lange syndrome 1, MIM# 122470; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NIPBL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:44:56.484344+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NIPAL4 as ready",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:44:56.476487+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nipal4 has been classified as Green List (High Evidence).",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:44:53.132816+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NIPAL4 were changed from Ichthyosis, autosomal recessive to Ichthyosis, congenital, autosomal recessive 6, MIM# 612281",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:44:41.792394+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NIPAL4 were set to ",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:44:25.534182+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NIPAL4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ichthyosis, congenital, autosomal recessive 6, MIM# 612281; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:44:21.483849+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.438",
"user_name": "David Amor",
"item_type": "entity",
"text": "reviewed gene: OFD1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Orofaciodigital syndrome I; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "OFD1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:43:25.832775+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NHLRC1 as ready",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:43:25.823380+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nhlrc1 has been classified as Red List (Low Evidence).",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:43:22.447122+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NHLRC1 were changed from Myoclonic epilepsy of Lafora to Epilepsy, progressive myoclonic 2B (Lafora), MIM# 254780",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:43:09.920886+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NHLRC1 as Red List (low evidence)",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:43:09.909120+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nhlrc1 has been classified as Red List (Low Evidence).",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:42:57.868307+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NHLRC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Epilepsy, progressive myoclonic 2B (Lafora), MIM# 254780; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:42:04.484885+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NHEJ1 as ready",
"entity_name": "NHEJ1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:42:04.469690+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nhej1 has been classified as Green List (High Evidence).",
"entity_name": "NHEJ1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:41:57.678186+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: NHEJ1.",
"entity_name": "NHEJ1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:41:48.697750+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NHEJ1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation, MIM# 611291; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NHEJ1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:41:09.532238+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NGLY1 as ready",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:41:09.523713+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ngly1 has been classified as Red List (Low Evidence).",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:41:06.096006+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NGLY1 were changed from Developmental delay, multifocal epilepsy & abnormal liver function to Congenital disorder of deglycosylation, MIM# 615273",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:40:55.794226+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NGLY1 as Red List (low evidence)",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:40:55.784935+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ngly1 has been classified as Red List (Low Evidence).",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:40:42.069575+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NGLY1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of deglycosylation, MIM# 615273; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:40:08.014190+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NF2 as ready",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:40:08.005894+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nf2 has been classified as Red List (Low Evidence).",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:40:04.454061+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NF2 were changed from Neurofibromatosis 2 to Neurofibromatosis, type 2 (MIM# 101000)",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:39:52.714450+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NF2 as Red List (low evidence)",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:39:52.687873+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nf2 has been classified as Red List (Low Evidence).",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:39:41.252397+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NF2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurofibromatosis, type 2 (MIM# 101000); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:38:29.597372+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NF1 as ready",
"entity_name": "NF1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:38:29.587600+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nf1 has been classified as Green List (High Evidence).",
"entity_name": "NF1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:38:26.494257+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NF1 were changed from Neurofibromatosis, type 1 to Neurofibromatosis, type 1, MIM# 162200",
"entity_name": "NF1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:38:16.212554+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.431",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NF1 were set to ",
"entity_name": "NF1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:38:02.309780+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NF1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurofibromatosis, type 1, MIM# 162200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NF1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:36:50.585854+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEUROG3 as ready",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:36:50.566819+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neurog3 has been classified as Green List (High Evidence).",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:36:43.504648+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: NEUROG3.",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:36:31.981306+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEUROG3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Diarrhoea 4, malabsorptive, congenital, MIM# 610370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:35:46.086479+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEU1 as ready",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:35:46.078245+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neu1 has been classified as Red List (Low Evidence).",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:35:42.040964+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEU1 were changed from Sialidosis to Sialidosis, type I and type II, MIM# 256550",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:35:30.483889+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.429",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEU1 as Red List (low evidence)",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:35:30.476353+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.429",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neu1 has been classified as Red List (Low Evidence).",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:35:17.945935+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEU1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Sialidosis, type I and type II, MIM# 256550; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:34:26.490969+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEK8 as ready",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:34:26.481980+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nek8 has been classified as Red List (Low Evidence).",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:34:14.374467+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEK8 as Red List (low evidence)",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:34:14.365932+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nek8 has been classified as Red List (Low Evidence).",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:34:01.662215+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEK8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Renal-hepatic-pancreatic dysplasia 2, MIM# 615415; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:33:23.249132+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEK1 as ready",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:33:23.240560+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nek1 has been classified as Red List (Low Evidence).",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:33:17.280304+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEK1 as Red List (low evidence)",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:33:17.271243+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nek1 has been classified as Red List (Low Evidence).",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:33:03.770378+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEK1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Short-rib thoracic dysplasia 6 with or without polydactyly, MIM# 263520; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:32:30.866927+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEFL as ready",
"entity_name": "NEFL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:32:30.855582+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nefl has been classified as Red List (Low Evidence).",
"entity_name": "NEFL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:32:25.457449+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEFL were changed from Charcot-Marie-Tooth disease to Charcot-Marie-Tooth disease, dominant intermediate G, MIM# 617882; Charcot-Marie-Tooth disease, type 1F, MIM# 607734; Charcot-Marie-Tooth disease, type 2E 607684",
"entity_name": "NEFL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:32:16.772867+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.425",
"user_name": "David Amor",
"item_type": "entity",
"text": "reviewed gene: OCRL: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Lowe syndrome; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "OCRL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:32:13.062414+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NEFL was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "NEFL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:32:03.647298+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEFL as Red List (low evidence)",
"entity_name": "NEFL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:32:03.583216+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nefl has been classified as Red List (Low Evidence).",
"entity_name": "NEFL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:31:49.380694+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.423",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEFL: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Charcot-Marie-Tooth disease, dominant intermediate G, MIM# 617882, Charcot-Marie-Tooth disease, type 1F, MIM# 607734, Charcot-Marie-Tooth disease, type 2E 607684; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "NEFL",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:31:04.539055+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.423",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEB as ready",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:31:04.529280+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.423",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neb has been classified as Red List (Low Evidence).",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:31:00.880906+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.423",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEB were changed from Nemaline myopathy to Nemaline myopathy 2, autosomal recessive 256030; Arthrogryposis multiplex congenita 6, MIM# 619334",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:30:49.501720+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEB as Red List (low evidence)",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:30:49.492918+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neb has been classified as Red List (Low Evidence).",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:30:37.725306+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Nemaline myopathy 2, autosomal recessive 256030, Arthrogryposis multiplex congenita 6, MIM# 619334; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:29:51.676185+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDP as ready",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:29:51.666574+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndp has been classified as Red List (Low Evidence).",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:29:47.930278+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDP were changed from Norrie disease to Norrie disease, MIM# 310600",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:29:35.057051+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.420",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDP as Red List (low evidence)",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:29:35.041942+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.420",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndp has been classified as Red List (Low Evidence).",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:29:23.231924+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.419",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Norrie disease, MIM# 310600; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:28:07.819987+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.419",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCF2 as ready",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:28:07.808698+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.419",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncf2 has been classified as Green List (High Evidence).",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:28:02.096534+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.419",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCF2 were set to ",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-10-06T13:27:51.847593+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: NCF2.",
"entity_name": "NCF2",
"entity_type": "gene"
}
]
}