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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=908",
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"results": [
{
"created": "2022-03-28T15:55:52.043598+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12148",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CASP10: Rating: GREEN; Mode of pathogenicity: None; Publications: 34329798, 34384744, 20301287; Phenotypes: Autoimmune lymphoproliferative syndrome, type II MIM#603909; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "CASP10",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:55:03.150918+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4634",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUBPL as ready",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:55:03.138523+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4634",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nubpl has been classified as Green List (High Evidence).",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:54:50.237204+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUBPL as ready",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:54:50.224887+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nubpl has been classified as Green List (High Evidence).",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:54:45.415807+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUBPL as ready",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:54:45.403893+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nubpl has been classified as Green List (High Evidence).",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:54:43.705335+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4634",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUBPL were changed from to Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:54:40.670772+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUBPL were changed from Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242 to Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:54:20.612899+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUBPL were changed from to Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:54:07.557353+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUBPL were changed from to Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:53:15.074527+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NUBPL were set to ",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:53:00.671993+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NUBPL were set to ",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:52:50.471309+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4633",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NUBPL were set to ",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:52:17.436167+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NUBPL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:52:12.047602+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.460",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NUBPL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:51:45.944607+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NUBPL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:50:55.372164+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LGI1 as ready",
"entity_name": "LGI1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:50:55.362004+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lgi1 has been classified as Green List (High Evidence).",
"entity_name": "LGI1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:50:52.221133+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LGI1 were changed from to Epilepsy, familial temporal lobe, 1, MIM# 6000512",
"entity_name": "LGI1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:50:16.123154+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LGI1 were set to ",
"entity_name": "LGI1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:49:29.754619+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LGI1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "LGI1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:49:00.562715+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LGI1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "LGI1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:47:55.319504+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LGI1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18711109, 12205652, 15079010, 22496201; Phenotypes: Epilepsy, familial temporal lobe, 1, MIM# 6000512; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "LGI1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:45:54.312707+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NTRK1 as ready",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:45:54.299533+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ntrk1 has been classified as Green List (High Evidence).",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:45:45.536912+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NTRK1 were changed from to Insensitivity to pain, congenital, with anhidrosis - MIM#256800",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:44:43.260026+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NTRK1 were set to ",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:44:04.903302+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NTRK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:43:34.243158+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4631",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NTRK1 as ready",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:43:34.232565+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4631",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ntrk1 has been classified as Green List (High Evidence).",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:43:28.257657+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4631",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NTRK1 were changed from to Insensitivity to pain, congenital, with anhidrosis - MIM#256800",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:41:48.108761+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4630",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NTRK1 were set to ",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:41:13.482627+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4629",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NTRK1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:40:43.279799+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4628",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NTRK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:39:46.618363+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NTF4 as ready",
"entity_name": "NTF4",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:39:46.606848+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ntf4 has been classified as Red List (Low Evidence).",
"entity_name": "NTF4",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:39:38.557683+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NTF4 were changed from to Glaucoma 1, open angle, 1O - MIIM#613100",
"entity_name": "NTF4",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:39:18.397980+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NTF4 were set to ",
"entity_name": "NTF4",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:58.641332+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NTF4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NTF4",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:45.692809+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12139",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CASK were changed from FG syndrome 4 MIM#300422; Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia MIM#300749; Mental retardation, with or without nystagmus MIM#300422 to FG syndrome 4 MIM#300422; Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia MIM#300749; Mental retardation, with or without nystagmus MIM#300422",
"entity_name": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:39.560397+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NTF4 as Red List (low evidence)",
"entity_name": "NTF4",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:39.550820+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ntf4 has been classified as Red List (Low Evidence).",
"entity_name": "NTF4",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:31.720589+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12138",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CASK were changed from to FG syndrome 4 MIM#300422; Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia MIM#300749; Mental retardation, with or without nystagmus MIM#300422",
"entity_name": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:14.454775+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12137",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CASK as ready",
"entity_name": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:14.446578+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12137",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cask has been classified as Green List (High Evidence).",
"entity_name": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:13.849192+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12137",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CASK as ready",
"entity_name": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:13.839256+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12137",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cask has been classified as Green List (High Evidence).",
"entity_name": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:38:04.856752+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12137",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CASK were set to ",
"entity_name": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:37:50.764032+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12136",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CASK 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": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:37:41.341785+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NSUN2 as ready",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:37:41.332437+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nsun2 has been classified as Green List (High Evidence).",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:37:32.834220+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NSUN2 were changed from to Mental retardation, autosomal recessive 5 - MIM#611091",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:37:25.517531+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12134",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CASK: Rating: GREEN; Mode of pathogenicity: None; Publications: 24278995; Phenotypes: FG syndrome 4 MIM#300422, Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia MIM#300749, Mental retardation, with or without nystagmus MIM#300422; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males); Current diagnostic: yes",
"entity_name": "CASK",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:37:11.896156+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NSUN2 were set to ",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:36:48.332744+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NSUN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:34:05.940134+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NSUN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 22541559, 22541562, 21063731, 22577224, 35126837; Phenotypes: Mental retardation, autosomal recessive 5 - MIM#611091; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:32:46.006671+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NSUN2 as ready",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:32:45.988567+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nsun2 has been classified as Green List (High Evidence).",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:32:38.252589+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NSUN2 were changed from to Mental retardation, autosomal recessive 5 - MIM#611091",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:31:46.752237+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4626",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NSUN2 were set to ",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:31:07.323354+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4625",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NSUN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:30:34.258568+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NSUN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 35126837; Phenotypes: Mental retardation, autosomal recessive 5 - MIM#611091; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:27:08.647107+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NRXN1 as ready",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:27:08.635492+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nrxn1 has been classified as Green List (High Evidence).",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:26:51.656881+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NRXN1 were changed from to Pitt-Hopkins-like syndrome 2 - MIM#614325",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:26:23.751363+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NRXN1 were set to ",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:26:05.023688+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NRXN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:25:34.997557+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NRXN1 as ready",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:25:34.985186+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nrxn1 has been classified as Green List (High Evidence).",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:24:37.960081+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12129",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CARD11 were changed from Immunodeficiency 11A, autosomal recessive, MIM# 615206; Immunodeficiency 11B with atopic dermatitis, autosomal dominant, MIM# 617638 to Immunodeficiency 11A, autosomal recessive, MIM# 615206; Immunodeficiency 11B with atopic dermatitis, autosomal dominant, MIM# 617638",
"entity_name": "CARD11",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:24:18.676387+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NRXN1 were changed from to Pitt-Hopkins-like syndrome 2 - MIM#614325",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:24:10.816990+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12128",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CARD11 were changed from to Immunodeficiency 11A, autosomal recessive, MIM# 615206; Immunodeficiency 11B with atopic dermatitis, autosomal dominant, MIM# 617638",
"entity_name": "CARD11",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:24:10.060922+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12128",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CARD11 as ready",
"entity_name": "CARD11",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:24:10.050564+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12128",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: card11 has been classified as Green List (High Evidence).",
"entity_name": "CARD11",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:24:02.439709+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12128",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CARD11 were set to ",
"entity_name": "CARD11",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:23:49.085670+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NRXN1 were set to ",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:23:38.436352+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12128",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CARD11 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CARD11",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:23:18.706586+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NRXN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:23:11.948328+11:00",
"panel_name": "Ataxia - paediatric",
"panel_id": 271,
"panel_version": "0.332",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CACNA2D2 as ready",
"entity_name": "CACNA2D2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:23:11.904620+11:00",
"panel_name": "Ataxia - paediatric",
"panel_id": 271,
"panel_version": "0.332",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cacna2d2 has been classified as Green List (High Evidence).",
"entity_name": "CACNA2D2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:23:08.799581+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12127",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CARD11: Rating: GREEN; Mode of pathogenicity: None; Publications: 23561803, 12818158, 23374270, 28628108; Phenotypes: Immunodeficiency 11A, autosomal recessive, MIM# 615206, Immunodeficiency 11B with atopic dermatitis, autosomal dominant, MIM# 617638; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "CARD11",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:22:39.256988+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NRXN1 were changed from Pitt-Hopkins-like syndrome 2 - MIM#614325 to Pitt-Hopkins-like syndrome 2 - MIM#614325",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:22:37.301882+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NRXN1 as ready",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:22:37.290407+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nrxn1 has been classified as Green List (High Evidence).",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:22:06.679437+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NRXN1 were changed from to Pitt-Hopkins-like syndrome 2 - MIM#614325",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:21:44.981593+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12127",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CALM3 as ready",
"entity_name": "CALM3",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:21:44.967550+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12127",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: calm3 has been classified as Green List (High Evidence).",
"entity_name": "CALM3",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:21:31.859757+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12127",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CALM3 were changed from to Long QT syndrome 16 MIM#618782; CPVT",
"entity_name": "CALM3",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:21:19.654016+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12127",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CALM3 were set to ",
"entity_name": "CALM3",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:21:16.386895+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12127",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CALM3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CALM3",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:21:10.337709+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1524",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NRXN1 were set to ",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:20:53.130901+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12126",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CALM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31983240; Phenotypes: Long QT syndrome 16 MIM#618782, CPVT; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "CALM3",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:20:29.280753+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NRXN1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:19:56.267183+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NRXN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:19:20.302338+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12126",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CALM2 as ready",
"entity_name": "CALM2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:19:20.289015+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12126",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: calm2 has been classified as Green List (High Evidence).",
"entity_name": "CALM2",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:18:56.061855+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NRXN1 as ready",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:18:56.052366+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nrxn1 has been classified as Green List (High Evidence).",
"entity_name": "NRXN1",
"entity_type": "gene"
},
{
"created": "2022-03-28T15:18:51.386300+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NRXN1 were changed from to Pitt-Hopkins-like syndrome 2 - MIM#614325",
"entity_name": "NRXN1",
"entity_type": "gene"
}
]
}