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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1868",
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"results": [
{
"created": "2020-04-12T13:59:00.533652+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRAF3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRAF3",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:58:36.773030+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAF3 as Red List (low evidence)",
"entity_name": "TRAF3",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:58:36.764423+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: traf3 has been classified as Red List (Low Evidence).",
"entity_name": "TRAF3",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:56:58.682953+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRAF3: Rating: RED; Mode of pathogenicity: None; Publications: 20832341; Phenotypes: {?Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 5}, MIM# 614849; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRAF3",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:46:58.109783+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TPP1 as ready",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:46:58.096056+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpp1 has been classified as Red List (Low Evidence).",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:46:55.584961+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TPP1 were changed from to Hoyeraal-Hreidarsson syndrome",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:46:32.373582+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.151",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TPP1 were set to ",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:46:06.397724+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TPP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:45:42.999639+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TPP1 as Red List (low evidence)",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:45:42.986634+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpp1 has been classified as Red List (Low Evidence).",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:45:13.150215+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TPP1: Rating: RED; Mode of pathogenicity: None; Publications: 25233904; Phenotypes: Hoyeraal-Hreidarsson syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:38:20.833065+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFSF12 as ready",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:38:20.823983+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfsf12 has been classified as Red List (Low Evidence).",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:38:10.441945+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFSF12 were changed from to Recurrent infections, poor antibody responses, decreased immunoglobulins",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:37:49.478837+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFSF12 were set to ",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:37:27.511539+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFSF12 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:37:10.094229+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFSF12 as Red List (low evidence)",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:37:10.080659+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfsf12 has been classified as Red List (Low Evidence).",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:36:50.650191+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFSF12: Rating: RED; Mode of pathogenicity: None; Publications: 23493554; Phenotypes: Recurrent infections, poor antibody responses, decreased immunoglobulins; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:36:04.432192+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFSF12 as ready",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:36:04.422663+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfsf12 has been classified as Red List (Low Evidence).",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:36:00.324012+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFSF12 were changed from to Recurrent infections, poor antibody responses, decreased immunoglobulins",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:35:30.426464+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFSF12 were set to ",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:34:59.062572+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFSF12 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:34:35.605532+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFSF12 as Red List (low evidence)",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:34:35.596204+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfsf12 has been classified as Red List (Low Evidence).",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:34:06.079035+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFSF12: Rating: RED; Mode of pathogenicity: None; Publications: 23493554; Phenotypes: Recurrent infections, poor antibody responses, decreased immunoglobulins; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNFSF12",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:19:46.318620+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFRSF4 as ready",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:19:46.309322+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf4 has been classified as Red List (Low Evidence).",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:19:38.731518+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFRSF4 were changed from to Immunodeficiency 16, MIM# 615593",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:19:18.321245+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFRSF4 were set to ",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:18:31.792420+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2155",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFRSF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:18:12.340150+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFRSF4 as Red List (low evidence)",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:18:12.327125+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf4 has been classified as Red List (Low Evidence).",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:17:26.765156+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFRSF4: Rating: RED; Mode of pathogenicity: None; Publications: 23897980; Phenotypes: Immunodeficiency 16, MIM# 615593; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:16:52.102038+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TNFRSF4: Changed phenotypes: Immunodeficiency 16, MIM# 615593",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:16:14.018285+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFRSF4 as ready",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:16:13.995799+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf4 has been classified as Red List (Low Evidence).",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:15:48.041460+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFRSF4 were changed from to Immunodeficiency 16, MIM# 615593",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:15:13.533288+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFRSF4 were set to ",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:14:49.278909+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFRSF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:14:14.774949+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFRSF4 as Red List (low evidence)",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:14:14.766021+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf4 has been classified as Red List (Low Evidence).",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T13:13:44.026781+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFRSF4: Rating: RED; Mode of pathogenicity: None; Publications: 23897980; Phenotypes: Immunodeficiency, MIM# 16; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFRSF4",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:41:16.857501+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFRSF13C as ready",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:41:16.849069+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf13c has been classified as Amber List (Moderate Evidence).",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:40:42.969110+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFRSF13C were changed from to Immunodeficiency, common variable, 4, MIM# 613494",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:40:21.336130+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFRSF13C were set to ",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:40:00.932107+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2151",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFRSF13C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:39:39.773983+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFRSF13C as Amber List (moderate evidence)",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:39:39.760983+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf13c has been classified as Amber List (Moderate Evidence).",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:39:21.534626+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFRSF13C: Rating: AMBER; Mode of pathogenicity: None; Publications: 19666484, 26613719; Phenotypes: Immunodeficiency, common variable, 4, MIM# 613494; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:38:40.024003+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFRSF13C as ready",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:38:40.009342+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf13c has been classified as Amber List (Moderate Evidence).",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:38:36.885645+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFRSF13C were changed from to Immunodeficiency, common variable, 4, MIM# 613494",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:38:13.327103+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFRSF13C were set to ",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:37:43.322557+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFRSF13C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:37:16.460960+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFRSF13C as Amber List (moderate evidence)",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:37:16.452119+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf13c has been classified as Amber List (Moderate Evidence).",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:36:46.424289+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFRSF13C: Rating: AMBER; Mode of pathogenicity: None; Publications: 19666484, 26613719; Phenotypes: Immunodeficiency, common variable, 4, MIM# 613494; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFRSF13C",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:36:43.140203+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.322",
"user_name": "Kristin Rigbye",
"item_type": "entity",
"text": "reviewed gene: NDUFS4: Rating: GREEN; Mode of pathogenicity: None; Publications: 10944442, 27079373, 19107570, 12616398; Phenotypes: Mitochondrial complex I deficiency, nuclear type 1, 252010, Leigh syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS4",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:20:17.767380+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFRSF13B as ready",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:20:17.758694+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf13b has been classified as Green List (High Evidence).",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:20:05.638111+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFRSF13B were changed from to Immunodeficiency, common variable, 2, MIM# 240500",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T12:19:46.608878+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFRSF13B were set to ",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T11:48:56.500674+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFRSF13B was changed from Unknown to Other",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T11:48:28.061808+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFRSF13B: Rating: GREEN; Mode of pathogenicity: None; Publications: 17392798, 16007086, 18981294, 16007087; Phenotypes: Immunodeficiency, common variable, 2, MIM# 240500; Mode of inheritance: Other",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T11:44:01.054088+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFRSF13B as ready",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T11:44:01.045239+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf13b has been classified as Green List (High Evidence).",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T11:43:58.140868+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFRSF13B were changed from to Immunodeficiency, common variable, 2, MIM# 240500",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T11:43:27.958739+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFRSF13B were set to ",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T11:42:55.920346+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFRSF13B was changed from Unknown to Other",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T11:42:25.282567+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFRSF13B: Rating: GREEN; Mode of pathogenicity: None; Publications: 17392798, 16007086, 18981294, 16007087; Phenotypes: Immunodeficiency, common variable, 2, MIM# 240500; Mode of inheritance: Other",
"entity_name": "TNFRSF13B",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:06:52.433390+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TINF2 as ready",
"entity_name": "TINF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:06:52.419942+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tinf2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TINF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:06:35.764615+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TINF2 were changed from to Dyskeratosis congenita, autosomal dominant 3, MIM# 613990; Revesz syndrome, MIM# 268130",
"entity_name": "TINF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:05:57.186904+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TINF2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TINF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:05:27.855772+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TINF2 as Amber List (moderate evidence)",
"entity_name": "TINF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:05:27.847146+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tinf2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TINF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:04:58.935492+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TINF2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Dyskeratosis congenita, autosomal dominant 3, MIM# 613990, Revesz syndrome, MIM# 268130; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TINF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:00:23.496771+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: THBD as ready",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:00:23.483677+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: thbd has been classified as Amber List (Moderate Evidence).",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T09:00:15.222283+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: THBD were changed from to {Hemolytic uremic syndrome, atypical, susceptibility to, 6}, MIM# 612926",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:59:54.113150+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: THBD were set to ",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:59:31.320003+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: THBD was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:58:57.760249+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: THBD as Amber List (moderate evidence)",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:58:57.747098+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: thbd has been classified as Amber List (Moderate Evidence).",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:58:38.934123+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: THBD: Rating: AMBER; Mode of pathogenicity: None; Publications: 29500241, 19625716; Phenotypes: {Hemolytic uremic syndrome, atypical, susceptibility to, 6}, MIM# 612926; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:57:42.186515+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: THBD as ready",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:57:42.177227+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: thbd has been classified as Red List (Low Evidence).",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:57:38.896573+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: THBD were changed from to {Hemolytic uremic syndrome, atypical, susceptibility to, 6}, MIM# 612926",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:57:08.532220+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: THBD were set to ",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:56:37.940419+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: THBD was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:56:09.303161+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: THBD as Red List (low evidence)",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:56:09.289797+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: thbd has been classified as Red List (Low Evidence).",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:55:34.772659+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: THBD: Rating: RED; Mode of pathogenicity: None; Publications: 29500241, 19625716; Phenotypes: {Hemolytic uremic syndrome, atypical, susceptibility to, 6}, MIM# 612926; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:53:20.369840+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAPBP as ready",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:53:20.355591+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tapbp has been classified as Red List (Low Evidence).",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-12T08:53:12.012853+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAPBP were changed from to Bare lymphocyte syndrome, type I, MIM# 604571",
"entity_name": "TAPBP",
"entity_type": "gene"
}
]
}