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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=919",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=917",
"results": [
{
"created": "2022-03-23T18:13:56.627096+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11836",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NLGN3 were set to ",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:11:49.165070+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NLGN3 were changed from to X-linked complex neurodevelopmental disorder MONDO:0100148; {Asperger syndrome susceptibility, X-linked 1} - MIM#300494; {Autism susceptibility, X-linked 1} - MIM#300425",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:11:06.995938+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NLGN3 as ready",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:11:06.985722+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nlgn3 has been classified as Green List (High Evidence).",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:11:04.063746+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NLGN3 were changed from {Asperger syndrome susceptibility, X-linked 1} - MIM#300494; {Autism susceptibility, X-linked 1} - MIM#300425 to X-linked complex neurodevelopmental disorder MONDO:0100148; {Asperger syndrome susceptibility, X-linked 1} - MIM#300494; {Autism susceptibility, X-linked 1} - MIM#300425",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:10:04.033662+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11834",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NLRC4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25217959, 25385754, 25217960; Phenotypes: ?Familial cold autoinflammatory syndrome 4 - MIM#616115, Autoinflammation with infantile enterocolitis - MIM#616050; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NLRC4",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:10:00.370538+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.134",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NLRC4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25217959, 25385754, 25217960; Phenotypes: ?Familial cold autoinflammatory syndrome 4 - MIM#616115, Autoinflammation with infantile enterocolitis - MIM#616050; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NLRC4",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:09:47.809394+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NLGN3 were changed from to {Asperger syndrome susceptibility, X-linked 1} - MIM#300494; {Autism susceptibility, X-linked 1} - MIM#300425",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:09:16.584818+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NLGN3 were set to ",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:08:41.492696+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NLGN3 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T18:08:22.128299+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NLGN3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NLGN3",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:35:45.623674+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NKX3-2 as ready",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:35:45.609830+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nkx3-2 has been classified as Green List (High Evidence).",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:35:36.668753+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NKX3-2 were changed from to Spondylo-megaepiphyseal-metaphyseal dysplasia - MIM#613330",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:35:13.514761+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NKX3-2 were set to ",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:32:57.435651+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11832",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NKX3-2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:30:50.895338+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NKX3-2 as ready",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:30:50.883151+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nkx3-2 has been classified as Green List (High Evidence).",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:30:48.523136+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NKX3-2 were changed from to Spondylo-megaepiphyseal-metaphyseal dysplasia (MIM#613330)",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:29:57.173746+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NKX3-2 were set to ",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:29:23.345998+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NKX3-2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:28:16.880141+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NIPAL4 as ready",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:28:16.871102+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11831",
"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": "2022-03-23T17:26:49.160097+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NIPAL4 were changed from to Ichthyosis, congenital, autosomal recessive 6 - MIM#612281",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:26:29.363531+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NIPAL4 were set to ",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:26:09.556679+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NIPAL4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:17:09.482597+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NHS as ready",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:17:09.472683+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nhs has been classified as Green List (High Evidence).",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:16:45.372228+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NHS were changed from to Nance-Horan syndrome - MIM#302350; Cataract 40, X-linked - MIM#302200",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:14:18.018667+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NHS were set to ",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:13:43.912647+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4587",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NHS was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:12:51.730313+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NHS as ready",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:12:51.719103+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nhs has been classified as Green List (High Evidence).",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:12:44.182246+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NHS were changed from to Nance-Horan syndrome - MIM#302350; Cataract 40, X-linked - MIM#302200",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:12:20.713472+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NHS were set to ",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:11:57.117704+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11826",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NHS was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:11:11.599851+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NFKBIL1 as ready",
"entity_name": "NFKBIL1",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:11:11.590456+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfkbil1 has been classified as Red List (Low Evidence).",
"entity_name": "NFKBIL1",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:11:02.347891+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NFKBIL1 were changed from to {Rheumatoid arthritis, susceptibility to} - MIM#180300",
"entity_name": "NFKBIL1",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:09:35.629751+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NFKBIL1 as Red List (low evidence)",
"entity_name": "NFKBIL1",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:09:35.620130+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfkbil1 has been classified as Red List (Low Evidence).",
"entity_name": "NFKBIL1",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:08:42.133419+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NFIA as ready",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:08:42.124311+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfia has been classified as Green List (High Evidence).",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:08:39.426167+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NFIA were changed from to Brain malformations with or without urinary tract defects - MIM#613735",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:08:10.071229+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.423",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFIA were set to ",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:07:39.971703+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NFIA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:06:53.693373+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11823",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NFIA as ready",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:06:53.681569+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11823",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfia has been classified as Green List (High Evidence).",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:06:45.317322+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11823",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NFIA were changed from to Brain malformations with or without urinary tract defects - MIM#613735",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:06:00.798181+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11822",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFIA were set to ",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:05:39.800115+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NFIA was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:03:37.797662+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NFIA as Green List (high evidence)",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:03:37.759901+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfia has been classified as Green List (High Evidence).",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:03:36.242044+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11820",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NFIA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:01:01.743545+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NFIA was added\ngene: NFIA was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic. Sources: Expert Review\nMode of inheritance for gene: NFIA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NFIA were set to 35018717; 33973697; 32926563\nPhenotypes for gene: NFIA were set to Brain malformations with or without urinary tract defects - MIM#613735\nReview for gene: NFIA was set to GREEN\nAdded comment: Haploinsufficiency of the NFIA gene causes NFIA-related disorder, which includes brain abnormalities and intellectual disability, with or without urinary tract defects. \nSources: Expert Review",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T17:00:47.782602+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NFIA were changed from to Brain malformations with or without urinary tract defects - MIM#613735",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:59:15.557900+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4585",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFIA were set to ",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:58:26.295660+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NFIA was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:58:02.175045+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NFIA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIA",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:57:04.787043+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEXN as ready",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:57:04.775033+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nexn has been classified as Green List (High Evidence).",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:56:56.803459+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEXN were changed from to Lethal fetal cardiomyopathy; Hydrops fetalis; Cardiomyopathy, dilated 1CC - MIM#613122",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:54:06.600691+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEXN were set to ",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:53:27.597426+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NEXN was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:52:53.414002+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEXN as ready",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:52:53.402448+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nexn has been classified as Red List (Low Evidence).",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:52:50.478389+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEXN were changed from to Lethal fetal cardiomyopathy; Hydrops fetalis; Cardiomyopathy, dilated 1CC - MIM#613122",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:52:21.435638+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.420",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEXN were set to ",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:51:45.469792+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.419",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NEXN was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:51:16.994774+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEXN as Red List (low evidence)",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:51:16.983706+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nexn has been classified as Red List (Low Evidence).",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:50:36.713164+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEXN as ready",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:50:36.704067+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nexn has been classified as Green List (High Evidence).",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:50:00.886021+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEXN as Green List (high evidence)",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:50:00.874130+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nexn has been classified as Green List (High Evidence).",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:49:29.448770+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEXN as ready",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:49:29.430173+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nexn has been classified as Green List (High Evidence).",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:48:28.217587+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEXN as Green List (high evidence)",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:48:28.207055+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nexn has been classified as Green List (High Evidence).",
"entity_name": "NEXN",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:42:03.273703+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4583",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STX1B as ready",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:42:03.260274+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4583",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stx1b has been classified as Green List (High Evidence).",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:41:56.457137+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4583",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STX1B were changed from to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:41:24.062098+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STX1B were set to ",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:40:49.147959+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:40:12.963676+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4580",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:38:54.186283+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STX1B as ready",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:38:54.172574+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stx1b has been classified as Green List (High Evidence).",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:38:50.550648+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STX1B were changed from to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:38:05.805595+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STX1B were set to ",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:37:14.340271+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:36:21.043760+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:35:58.914387+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: STX1B: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:35:26.595099+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STX1B as ready",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:35:26.583406+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stx1b has been classified as Green List (High Evidence).",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:35:17.344578+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STX1B were changed from to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:34:55.740042+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STX1B were set to ",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:32:28.567712+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11814",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:32:09.403488+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: None",
"entity_name": "STX1B",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:28:50.949819+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STX2 as ready",
"entity_name": "STX2",
"entity_type": "gene"
},
{
"created": "2022-03-23T16:28:50.938421+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stx2 has been classified as Red List (Low Evidence).",
"entity_name": "STX2",
"entity_type": "gene"
}
]
}