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{
"created": "2019-12-08T07:58:53.100812+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOP10 as ready",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:58:53.093928+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:58:48.892303+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NOP10 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:58:31.411298+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NOP10 were changed from to Dyskeratosis congenita, autosomal recessive 1, MIM#224230",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:58:13.567350+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:57:56.203224+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NOP10 were set to ",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:56:44.439676+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NOP10 as Red List (low evidence)",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:56:44.431986+11:00",
"panel_name": "Combined immunodeficiency_MelbourneGenomics_VCGS",
"panel_id": 223,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:56:05.149724+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOP10 as ready",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:56:05.142362+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:55:57.105707+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NOP10 were changed from to Dyskeratosis congenita, autosomal recessive 1, MIM#224230",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:55:42.182377+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NOP10 were set to ",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:55:23.794457+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:55:04.419964+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.199",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NOP10 as Red List (low evidence)",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:55:04.411652+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.199",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:54:38.361964+11:00",
"panel_name": "Cancer Predisposition_Paediatric_VCGS",
"panel_id": 152,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOP10 as ready",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:54:38.353826+11:00",
"panel_name": "Cancer Predisposition_Paediatric_VCGS",
"panel_id": 152,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:54:28.111808+11:00",
"panel_name": "Cancer Predisposition_Paediatric_VCGS",
"panel_id": 152,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:53:49.220451+11:00",
"panel_name": "Cancer Predisposition_Paediatric_VCGS",
"panel_id": 152,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NOP10 were changed from to Dyskeratosis congenita, autosomal recessive 1, MIM#224230",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:53:11.233882+11:00",
"panel_name": "Cancer Predisposition_Paediatric_VCGS",
"panel_id": 152,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NOP10 were set to ",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:52:47.829503+11:00",
"panel_name": "Cancer Predisposition_Paediatric_VCGS",
"panel_id": 152,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NOP10 as Red List (low evidence)",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:52:47.818142+11:00",
"panel_name": "Cancer Predisposition_Paediatric_VCGS",
"panel_id": 152,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:48:13.369509+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOP10 as ready",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:48:13.362149+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:48:09.398125+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NOP10 were changed from to Dyskeratosis congenita, autosomal recessive 1, MIM#224230",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:47:49.463924+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NOP10 were set to 17507419",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:47:21.293092+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NOP10 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:47:00.423667+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NOP10 as Red List (low evidence)",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:47:00.414964+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:46:43.990187+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NOP10 were set to ",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:46:27.475313+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:46:11.175895+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NOP10 as Red List (low evidence)",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:46:11.131620+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:45:41.957641+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NOP10: Rating: RED; Mode of pathogenicity: None; Publications: 17507419; Phenotypes: Dyskeratosis congenita, autosomal recessive 1, MIM#224230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:44:48.783237+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.874",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOP10 as ready",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:44:48.775771+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.874",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:44:43.467089+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.874",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NOP10 were changed from to Dyskeratosis congenita, autosomal recessive 1, MIM#224230",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:44:29.799058+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.873",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NOP10 were set to ",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:44:20.250251+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.872",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:44:13.401622+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.871",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NOP10 as Red List (low evidence)",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:44:13.392706+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.871",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop10 has been classified as Red List (Low Evidence).",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:44:00.124335+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.870",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NOP10: Rating: RED; Mode of pathogenicity: None; Publications: 17507419; Phenotypes: Dyskeratosis congenita, autosomal recessive 1, MIM#224230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NOP10",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:39:45.583914+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NIN as ready",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:39:45.576987+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nin has been classified as Red List (Low Evidence).",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:39:38.074495+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NIN were changed from to Seckel syndrome 7, MIM#614851",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:39:24.871275+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NIN were set to ",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:39:08.400195+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NIN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:38:45.584022+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NIN as Red List (low evidence)",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:38:45.575938+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nin has been classified as Red List (Low Evidence).",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:38:25.971456+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NIN: Rating: RED; Mode of pathogenicity: None; Publications: 22933543; Phenotypes: Seckel syndrome 7, MIM#614851; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:37:22.544644+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NIN as ready",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:37:22.537178+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nin has been classified as Red List (Low Evidence).",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:37:19.787387+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NIN were changed from to Seckel syndrome 7, MIM#614851",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:37:00.059409+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NIN were set to ",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:36:38.513453+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NIN as Red List (low evidence)",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:36:38.506507+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nin has been classified as Red List (Low Evidence).",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:36:13.108325+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NIN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:35:56.930664+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NIN as Red List (low evidence)",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:35:56.868521+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nin has been classified as Red List (Low Evidence).",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:33:22.871714+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NIN as ready",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:33:22.862733+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nin has been classified as Red List (Low Evidence).",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:33:18.773641+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NIN were changed from to Seckel syndrome 7, MIM#614851",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:32:57.684436+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NIN were set to ",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:32:34.169118+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NIN as Red List (low evidence)",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:32:34.162117+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nin has been classified as Red List (Low Evidence).",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:32:05.740837+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NIN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:31:49.181991+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NIN as Red List (low evidence)",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:31:49.167105+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nin has been classified as Red List (Low Evidence).",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:31:20.936425+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NIN: Rating: RED; Mode of pathogenicity: None; Publications: 22933543; Phenotypes: Seckel syndrome 7, MIM#614851; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:30:08.621543+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.870",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NIN: Rating: RED; Mode of pathogenicity: None; Publications: 22933543; Phenotypes: Seckel syndrome 7, MIM#614851; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NIN",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:22:43.936351+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.870",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NHLRC1 as ready",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:22:43.929474+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.870",
"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": "2019-12-08T07:22:39.239960+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.870",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NHLRC1 were changed from to Epilepsy, progressive myoclonic 2B (Lafora), MIM#254780",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:22:25.222478+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.869",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NHLRC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:22:18.686468+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.868",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NHLRC1 as Red List (low evidence)",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:22:18.678965+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.868",
"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": "2019-12-08T07:22:02.219245+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.867",
"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": "2019-12-08T07:19:08.897419+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.867",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NFIB as ready",
"entity_name": "NFIB",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:19:08.889817+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.867",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfib has been classified as Green List (High Evidence).",
"entity_name": "NFIB",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:19:04.316829+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.867",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NFIB as Green List (high evidence)",
"entity_name": "NFIB",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:19:04.309260+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.867",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfib has been classified as Green List (High Evidence).",
"entity_name": "NFIB",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:18:50.153791+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.866",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NFIB was added\ngene: NFIB was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: NFIB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NFIB were set to 30388402\nPhenotypes for gene: NFIB were set to Macrocephaly, acquired, with impaired intellectual development, MIM#618286\nReview for gene: NFIB was set to GREEN\nAdded comment: 18 individuals reported, of whom 11 had deletions of this gene and the rest had SNVs. \nSources: Expert list",
"entity_name": "NFIB",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:15:01.199132+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.865",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEGR1 as ready",
"entity_name": "NEGR1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:15:01.191334+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.865",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: negr1 has been classified as Red List (Low Evidence).",
"entity_name": "NEGR1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:14:52.520106+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.865",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEGR1 as Red List (low evidence)",
"entity_name": "NEGR1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:14:52.511414+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.865",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: negr1 has been classified as Red List (Low Evidence).",
"entity_name": "NEGR1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:14:39.451902+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.864",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEGR1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "NEGR1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:11:02.209364+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.864",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEDD4L as ready",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:11:02.198373+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.864",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nedd4l has been classified as Green List (High Evidence).",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:10:57.807755+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.864",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEDD4L were changed from to Periventricular nodular heterotopia 7, MIM#617201",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:10:40.281723+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.863",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NEDD4L was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:10:25.475281+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.862",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEDD4L: Rating: GREEN; Mode of pathogenicity: None; Publications: 27694961; Phenotypes: Periventricular nodular heterotopia 7, MIM#617201; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:06:28.465231+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NECAP1 as ready",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:06:28.458302+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: necap1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:06:20.471871+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NECAP1 were changed from to Epileptic encephalopathy, early infantile, 21, MIM#615833",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:06:01.849404+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NECAP1 were set to ",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:05:39.835477+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NECAP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:05:20.542791+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NECAP1 as Amber List (moderate evidence)",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:05:20.534544+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: necap1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:04:38.717336+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EXT2 were changed from to Seizures, scoliosis, and macrocephaly syndrome, MIM#616682",
"entity_name": "EXT2",
"entity_type": "gene"
}
]
}