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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1869",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1867",
"results": [
{
"created": "2020-04-12T08:52:56.303088+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAPBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:38:08.058520+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NXN were changed from to Robinow syndrome, autosomal recessive 2 618529",
"entity_name": "NXN",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:37:53.680091+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NXN were set to ",
"entity_name": "NXN",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:37:39.434938+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NXN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NXN",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:37:19.809842+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NXN: Rating: GREEN; Mode of pathogenicity: None; Publications: 29276006; Phenotypes: Robinow syndrome, autosomal recessive 2 618529; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NXN",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:05:54.161750+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TERT as ready",
"entity_name": "TERT",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:05:54.148539+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tert has been classified as Amber List (Moderate Evidence).",
"entity_name": "TERT",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:05:52.399445+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TAPBP were set to ",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:05:45.704044+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TERT were changed from to {Dyskeratosis congenita, autosomal dominant 2}, MIM# 613989; {Dyskeratosis congenita, autosomal recessive 4}, MIM# 613989",
"entity_name": "TERT",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:05:20.827797+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TERT was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TERT",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:04:48.736295+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TERT as Amber List (moderate evidence)",
"entity_name": "TERT",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:04:48.723369+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tert has been classified as Amber List (Moderate Evidence).",
"entity_name": "TERT",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:04:17.704533+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TERT: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: {Dyskeratosis congenita, autosomal dominant 2}, MIM# 613989, {Dyskeratosis congenita, autosomal recessive 4}, MIM# 613989; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TERT",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:03:04.824500+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TERC as ready",
"entity_name": "TERC",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:03:04.811023+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: terc has been classified as Amber List (Moderate Evidence).",
"entity_name": "TERC",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:02:28.611102+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TERC were changed from to Dyskeratosis congenita, autosomal dominant 1, MIM# 127550",
"entity_name": "TERC",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:02:00.589228+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TERC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TERC",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:01:36.879651+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TERC as Amber List (moderate evidence)",
"entity_name": "TERC",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:01:36.871160+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: terc has been classified as Amber List (Moderate Evidence).",
"entity_name": "TERC",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:01:05.892123+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TERC: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Dyskeratosis congenita, autosomal dominant 1, MIM# 127550; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TERC",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:00:15.470540+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TAPBP as Red List (low evidence)",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:00:15.455284+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2136",
"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": "2020-04-11T21:00:06.102857+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TAPBP as Red List (low evidence)",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T21:00:06.092524+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2136",
"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": "2020-04-11T20:58:23.316711+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TAPBP: Rating: RED; Mode of pathogenicity: None; Publications: 12149238; Phenotypes: Bare lymphocyte syndrome, type I, MIM# 604571; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:58:06.283588+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: TAPBP.",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:57:31.421543+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAPBP as ready",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:57:31.412478+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.135",
"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": "2020-04-11T20:57:28.591986+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.135",
"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"
},
{
"created": "2020-04-11T20:57:05.384012+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TAPBP were set to ",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:56:40.659932+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAPBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:56:17.066961+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TAPBP as Red List (low evidence)",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:56:17.058167+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.132",
"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": "2020-04-11T20:55:47.583749+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TAPBP: Rating: RED; Mode of pathogenicity: None; Publications: 12149238; Phenotypes: Bare lymphocyte syndrome, type I, MIM# 604571; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAPBP",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:21:22.808701+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SH3BP2 were changed from Cherubism, MIM# 118400 to Cherubism, MIM# 118400",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:21:14.791345+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SH3BP2 as ready",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:21:14.781468+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sh3bp2 has been classified as Red List (Low Evidence).",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:21:00.222115+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SH3BP2 were changed from Cherubism, MIM# 118400 to Cherubism, MIM# 118400",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:20:39.565873+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SH3BP2 were changed from to Cherubism, MIM# 118400",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:19:52.549732+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SH3BP2 were set to ",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:19:28.341069+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SH3BP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:18:52.250698+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SH3BP2 as Red List (low evidence)",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:18:52.237298+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sh3bp2 has been classified as Red List (Low Evidence).",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:18:22.005813+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SH3BP2: Rating: RED; Mode of pathogenicity: None; Publications: 26152156, 25705883, 25470448, 25220465; Phenotypes: Cherubism, MIM# 118400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SH3BP2",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:08:25.736618+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SEMA3E as ready",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T20:08:25.727957+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3e has been classified as Amber List (Moderate Evidence).",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:42:59.760950+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SEMA3E were changed from to CHARGE syndrome, MIM#214800",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:42:40.612696+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SEMA3E were set to ",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:42:17.193785+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SEMA3E was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:42:11.067892+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SEMA3E as Amber List (moderate evidence)",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:42:11.059109+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3e has been classified as Amber List (Moderate Evidence).",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:41:50.803055+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SEMA3E: Rating: AMBER; Mode of pathogenicity: None; Publications: 15235037, 31691538, 31464029; Phenotypes: CHARGE syndrome, MIM#214800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:40:21.504905+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SEMA3E as ready",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:40:21.491597+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3e has been classified as Red List (Low Evidence).",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:40:18.591589+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SEMA3E were changed from to CHARGE syndrome, MIM# 214800",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:39:54.824645+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SEMA3E were set to ",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:39:10.601799+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SEMA3E was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:38:41.219556+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SEMA3E as Red List (low evidence)",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:38:41.210668+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3e has been classified as Red List (Low Evidence).",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:38:08.676746+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SEMA3E: Rating: RED; Mode of pathogenicity: None; Publications: 15235037, 28634005; Phenotypes: CHARGE syndrome, MIM# 214800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:32:03.519010+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SAMD9 as ready",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:32:03.505479+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: samd9 has been classified as Green List (High Evidence).",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:31:59.672501+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SAMD9 were changed from to MIRAGE syndrome, MIM# 617053",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:31:30.178903+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SAMD9 were set to ",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:30:59.841607+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SAMD9 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2020-04-11T19:30:28.316112+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SAMD9: Rating: GREEN; Mode of pathogenicity: None; Publications: 31620126; Phenotypes: MIRAGE syndrome, MIM# 617053; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:46:29.547367+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNF31 as ready",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:46:29.534496+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf31 has been classified as Amber List (Moderate Evidence).",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:46:20.363350+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNF31 were changed from to Immune deficiency; Autoinflammation",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:46:00.480845+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RNF31 were set to ",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:45:45.591283+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RNF31 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:45:32.048098+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RNF31 as Amber List (moderate evidence)",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:45:32.034968+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf31 has been classified as Amber List (Moderate Evidence).",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:45:13.359150+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RNF31: Rating: AMBER; Mode of pathogenicity: None; Publications: 26008899, 30936877; Phenotypes: Immune deficiency, Autoinflammation; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:44:25.354346+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNF31 as ready",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:44:25.344861+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf31 has been classified as Amber List (Moderate Evidence).",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:44:22.625032+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNF31 were changed from to Immune deficiency; Autoinflammation",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:43:59.111242+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RNF31 were set to ",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:43:35.354676+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RNF31 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:43:11.591691+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RNF31 as Amber List (moderate evidence)",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:43:11.581582+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf31 has been classified as Amber List (Moderate Evidence).",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:42:40.791548+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RNF31: Rating: AMBER; Mode of pathogenicity: None; Publications: 26008899, 30936877; Phenotypes: Immune deficiency, Autoinflammation; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNF31",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:39:28.790653+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RHOH as ready",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:39:28.775884+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rhoh has been classified as Red List (Low Evidence).",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:39:06.909838+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RHOH were changed from to {?Epidermodysplasia verruciformis, susceptibility to, 4}, MIM# 618307",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:38:45.152892+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RHOH were set to ",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:38:31.448321+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RHOH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:38:17.128680+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RHOH as Red List (low evidence)",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:38:17.120060+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rhoh has been classified as Red List (Low Evidence).",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:37:49.699222+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RHOH: Rating: RED; Mode of pathogenicity: None; Publications: 22850876, 27574848; Phenotypes: {?Epidermodysplasia verruciformis, susceptibility to, 4}, MIM# 618307; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:37:40.689285+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RHOH as ready",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:37:40.675898+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rhoh has been classified as Red List (Low Evidence).",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:36:53.055241+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSMB9 as ready",
"entity_name": "PSMB9",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:36:53.046627+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psmb9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PSMB9",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:36:45.334011+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RHOH were changed from to {?Epidermodysplasia verruciformis, susceptibility to, 4}, MIM# 618307",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:36:17.487715+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RHOH were set to ",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:35:43.614762+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RHOH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:35:15.687345+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RHOH as Red List (low evidence)",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:35:15.678430+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rhoh has been classified as Red List (Low Evidence).",
"entity_name": "RHOH",
"entity_type": "gene"
},
{
"created": "2020-04-11T18:34:45.414989+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RHOH: Rating: RED; Mode of pathogenicity: None; Publications: 22850876, 27574848; Phenotypes: {?Epidermodysplasia verruciformis, susceptibility to, 4}, MIM# 618307; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RHOH",
"entity_type": "gene"
}
]
}