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{
"count": 220489,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=973",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=971",
"results": [
{
"created": "2022-02-23T15:49:37.489836+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3992",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLIT2 as Amber List (moderate evidence)",
"entity_name": "SLIT2",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:49:37.478398+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3992",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slit2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLIT2",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:49:09.748912+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3991",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ANKRD17 as ready",
"entity_name": "ANKRD17",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:49:09.733681+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3991",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ankrd17 has been classified as Green List (High Evidence).",
"entity_name": "ANKRD17",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:49:02.485974+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3991",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ANKRD17 as Green List (high evidence)",
"entity_name": "ANKRD17",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:49:02.465853+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3991",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ankrd17 has been classified as Green List (High Evidence).",
"entity_name": "ANKRD17",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:48:35.971431+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALB as ready",
"entity_name": "ALB",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:48:35.959607+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alb has been classified as Green List (High Evidence).",
"entity_name": "ALB",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:48:29.886840+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALB as Green List (high evidence)",
"entity_name": "ALB",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:48:29.874578+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alb has been classified as Green List (High Evidence).",
"entity_name": "ALB",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:47:50.877082+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3989",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACBD5 as ready",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:47:50.867298+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3989",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: acbd5 has been classified as Red List (Low Evidence).",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:47:43.885781+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3989",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ACBD5 as Red List (low evidence)",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:47:43.876271+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3989",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: acbd5 has been classified as Red List (Low Evidence).",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:46:53.908558+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3988",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF711 as ready",
"entity_name": "ZNF711",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:46:53.897730+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3988",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf711 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF711",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:46:47.376595+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3988",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF711 were changed from MENTAL RETARDATION X-LINKED ZNF711-RELATED to Mental retardation, X-linked 97, OMIM #300803",
"entity_name": "ZNF711",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:46:29.252898+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF711 were set to ",
"entity_name": "ZNF711",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:46:12.992439+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3986",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZNF711: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, X-linked 97, OMIM #300803; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "ZNF711",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:45:12.330103+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3986",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF3 as ready",
"entity_name": "ZNF3",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:45:12.308018+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3986",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf3 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF3",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:43:57.129836+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3986",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XPA as ready",
"entity_name": "XPA",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:43:57.117888+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3986",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpa has been classified as Red List (Low Evidence).",
"entity_name": "XPA",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:43:52.921188+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3986",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XPA were changed from XERODERMA PIGMENTOSUM, GROUP A to Xeroderma pigmentosum, group A, OMIM# 278700",
"entity_name": "XPA",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:43:39.408808+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3985",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XPA were set to ",
"entity_name": "XPA",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:43:23.672323+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3984",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Multiple families reported where ID is part of the phenotype, though some share haplotype and are likely distantly related.; to: Clinical presentation is typically post-natal.",
"entity_name": "XPA",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:43:09.897798+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3984",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: XPA: Changed rating: RED",
"entity_name": "XPA",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:42:43.233871+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3984",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR91 as ready",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:42:43.223836+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3984",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr91 has been classified as Amber List (Moderate Evidence).",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:42:36.012941+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3984",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WDR91 as Amber List (moderate evidence)",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:42:35.993500+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3984",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr91 has been classified as Amber List (Moderate Evidence).",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:41:59.389837+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3983",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR11 as ready",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:41:59.379553+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3983",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:41:54.271582+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3983",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR11 were changed from KALLMANN SYNDROME to Intellectual disability; Microcephaly; Short stature",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:41:40.203398+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3982",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR11 were set to ",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:41:27.273468+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3981",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR11 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:41:16.108853+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3980",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WDR11 as Amber List (moderate evidence)",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:41:16.091892+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3980",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:40:59.698442+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: WDR11: Changed rating: AMBER",
"entity_name": "WDR11",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:39:57.504154+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WASHC5 as ready",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:39:57.492480+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: washc5 has been classified as Red List (Low Evidence).",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:39:53.617839+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WASHC5 were changed from Ritscher-Schinzel syndrome 1 220210; Spastic paraplegia 8, autosomal dominant 603563 to Ritscher-Schinzel syndrome 1, MIM# 220210",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:39:39.015141+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3978",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WASHC5 were set to ",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:39:04.064033+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: WASHC5.",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:38:53.899352+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WASHC5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ritscher-Schinzel syndrome 1, MIM# 220210; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:36:43.583233+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WAC as ready",
"entity_name": "WAC",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:36:43.571520+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wac has been classified as Red List (Low Evidence).",
"entity_name": "WAC",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:36:39.726537+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WAC were changed from INTELLECTUAL DISABILITY; WAC syndrome to Desanto-Shinawi syndrome, MIM# 616708",
"entity_name": "WAC",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:36:27.376421+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WAC were set to ",
"entity_name": "WAC",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:36:16.240190+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3975",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WAC was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WAC",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:36:02.567704+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WAC: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Desanto-Shinawi syndrome, MIM# 616708; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WAC",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:34:12.149497+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UROC1 as ready",
"entity_name": "UROC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:34:12.138269+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uroc1 has been classified as Red List (Low Evidence).",
"entity_name": "UROC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:34:08.326478+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UROC1 were changed from UROCANASE DEFICIENCY to Urocanase deficiency, MIM#276880",
"entity_name": "UROC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:33:54.410590+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UROC1 were set to ",
"entity_name": "UROC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:33:09.547882+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UPF3B as ready",
"entity_name": "UPF3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:33:09.531582+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: upf3b has been classified as Red List (Low Evidence).",
"entity_name": "UPF3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:29:22.057648+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UPF3B were changed from MENTAL RETARDATION SYNDROMIC X-LINKED TYPE 14 to Mental retardation, X-linked, syndromic 14, MIM# 300676",
"entity_name": "UPF3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:29:04.262134+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3971",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UPF3B were set to ",
"entity_name": "UPF3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:23:07.661736+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Well established gene-disease association, more than 7 families reported, mouse model and other functional data.; to: Well established gene-disease association, more than 7 families reported, mouse model and other functional data. Clinical presentation is typically post-natal.",
"entity_name": "UPF3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:22:51.883101+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: UPF3B: Changed rating: RED",
"entity_name": "UPF3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:19:30.858060+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UNC80 as ready",
"entity_name": "UNC80",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:19:30.846802+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: unc80 has been classified as Red List (Low Evidence).",
"entity_name": "UNC80",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:18:35.871813+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UNC80 were set to ",
"entity_name": "UNC80",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:18:19.036400+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: UNC80: Changed rating: RED",
"entity_name": "UNC80",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:17:32.212389+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UFM1 as ready",
"entity_name": "UFM1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:17:32.197876+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ufm1 has been classified as Red List (Low Evidence).",
"entity_name": "UFM1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:17:27.619120+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UFM1 were changed from Severe early-onset encephalopathy with progressive microcephaly, to Leukodystrophy, hypomyelinating, 14 MIM#617899",
"entity_name": "UFM1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:17:13.219964+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UFM1 were set to 29868776",
"entity_name": "UFM1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:16:51.316381+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3967",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: UFM1: Added comment: Clinical presentation is typically post-natal.; Changed rating: RED; Changed phenotypes: Leukodystrophy, hypomyelinating, 14 MIM#617899; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UFM1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:15:16.127196+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3967",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UFC1 as ready",
"entity_name": "UFC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:15:16.115410+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3967",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ufc1 has been classified as Red List (Low Evidence).",
"entity_name": "UFC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:15:10.443953+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3967",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UFC1 were changed from Severe early-onset encephalopathy with progressive microcephaly to Neurodevelopmental disorder with spasticity and poor growth (MIM#618076)",
"entity_name": "UFC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:14:57.047827+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UFC1 were set to ",
"entity_name": "UFC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:14:39.063212+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3965",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UFC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with spasticity and poor growth (MIM#618076); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UFC1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:13:38.610811+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3965",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBE3A as ready",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:13:38.601581+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3965",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ube3a has been classified as Red List (Low Evidence).",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:13:34.079208+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3965",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBE3A were changed from ANGELMAN SYNDROME to Angelman syndrome MIM#105830",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:13:13.294368+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: UBE3A: Clinical presentation is typically post-natal.",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:12:38.236905+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: UBE3A: Changed rating: RED",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:09:42.877836+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBE2A as ready",
"entity_name": "UBE2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:09:42.862390+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ube2a has been classified as Red List (Low Evidence).",
"entity_name": "UBE2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:09:37.194484+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBE2A were changed from UBE2A-RELATED X-LINKED SYNDROMIC MENTAL RETARDATION to Mental retardation, X-linked syndromic, Nascimento-type (MIM#300860)",
"entity_name": "UBE2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:09:21.738192+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBE2A were set to ",
"entity_name": "UBE2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:09:02.582304+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UBE2A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, X-linked syndromic, Nascimento-type (MIM#300860); Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "UBE2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:07:35.247716+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBA5 as ready",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:07:35.237548+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uba5 has been classified as Red List (Low Evidence).",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:07:29.915811+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBA5 were changed from Severe Infantile-Onset Encephalopathy to Epileptic encephalopathy, early infantile, 44 (MIM#617132)",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:07:15.460922+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBA5 were set to ",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:06:58.042362+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UBA5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Epileptic encephalopathy, early infantile, 44 (MIM#617132); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:05:48.124186+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUSC3 as ready",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:05:48.114495+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tusc3 has been classified as Red List (Low Evidence).",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:05:43.955851+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUSC3 were changed from MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 7 to Mental retardation, autosomal recessive 7, MIM# 611093, MONDO:0012615; TUSC3-CDG (Disorders of protein N-glycosylation)",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:05:30.118226+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUSC3 were set to ",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:05:03.377710+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: More than 5 unrelated families reported, note homozygous deletions in at least two.; to: More than 5 unrelated families reported, note homozygous deletions in at least two. Clinical presentation is typically post-natal.",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:04:49.680434+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TUSC3: Changed rating: RED",
"entity_name": "TUSC3",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:03:59.318272+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM70 as ready",
"entity_name": "TMEM70",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:03:59.308783+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem70 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TMEM70",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:03:55.129365+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM70 were changed from MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2 to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2 MIM#614052",
"entity_name": "TMEM70",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:03:41.958090+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3957",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM70 were set to ",
"entity_name": "TMEM70",
"entity_type": "gene"
}
]
}