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{
"count": 220314,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2104",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2102",
"results": [
{
"created": "2019-11-20T21:13:38.919605+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cryl1 has been classified as Red List (Low Evidence).",
"entity_name": "CRYL1",
"entity_type": "gene"
},
{
"created": "2019-11-20T21:13:24.634031+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CRYL1 as Red List (low evidence)",
"entity_name": "CRYL1",
"entity_type": "gene"
},
{
"created": "2019-11-20T21:13:24.614868+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cryl1 has been classified as Red List (Low Evidence).",
"entity_name": "CRYL1",
"entity_type": "gene"
},
{
"created": "2019-11-20T21:13:01.654529+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYL1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "CRYL1",
"entity_type": "gene"
},
{
"created": "2019-11-20T21:11:23.595742+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IQCG as ready",
"entity_name": "IQCG",
"entity_type": "gene"
},
{
"created": "2019-11-20T21:11:23.584634+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: iqcg has been classified as Red List (Low Evidence).",
"entity_name": "IQCG",
"entity_type": "gene"
},
{
"created": "2019-11-20T21:11:13.028108+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IQCG as Red List (low evidence)",
"entity_name": "IQCG",
"entity_type": "gene"
},
{
"created": "2019-11-20T21:11:13.016436+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: iqcg has been classified as Red List (Low Evidence).",
"entity_name": "IQCG",
"entity_type": "gene"
},
{
"created": "2019-11-20T21:10:52.016381+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IQCG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "IQCG",
"entity_type": "gene"
},
{
"created": "2019-11-20T16:39:16.877451+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: VTN: Added comment: Over-representation in cases vs controls but no functional data and mechanism unclear at present.; Changed phenotypes: Atypical haemolytic uraemic syndrome",
"entity_name": "VTN",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:53:11.975252+11:00",
"panel_name": "Renal cystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal cystic disease_KidGen to Renal cystic disease_KidGen_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-20T15:51:23.544159+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DZIP1L as ready",
"entity_name": "DZIP1L",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:51:23.533008+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dzip1l has been classified as Green List (High Evidence).",
"entity_name": "DZIP1L",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:51:17.464917+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DZIP1L as Green List (high evidence)",
"entity_name": "DZIP1L",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:51:17.453610+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dzip1l has been classified as Green List (High Evidence).",
"entity_name": "DZIP1L",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:51:00.215919+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DZIP1L was added\ngene: DZIP1L was added to Renal cystic disease_KidGen. Sources: Expert list\nMode of inheritance for gene: DZIP1L was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DZIP1L were set to 28530676\nPhenotypes for gene: DZIP1L were set to Polycystic kidney disease 5, MIM#617610\nReview for gene: DZIP1L was set to GREEN\ngene: DZIP1L was marked as current diagnostic\nAdded comment: 7 individuals from 4 unrelated families with bi-allelic variants in this gene. \nSources: Expert list",
"entity_name": "DZIP1L",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:48:32.970095+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAJB11 as ready",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:48:32.958869+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajb11 has been classified as Green List (High Evidence).",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:48:27.784269+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAJB11 as Green List (high evidence)",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:48:27.772905+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajb11 has been classified as Green List (High Evidence).",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:48:15.507165+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DNAJB11 was added\ngene: DNAJB11 was added to Renal cystic disease_KidGen. Sources: Expert list\nMode of inheritance for gene: DNAJB11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DNAJB11 were set to 29706351; 29777155\nPhenotypes for gene: DNAJB11 were set to Polycystic kidney disease 6 with or without polycystic liver disease, MIM#618061\nReview for gene: DNAJB11 was set to GREEN\ngene: DNAJB11 was marked as current diagnostic\nAdded comment: Seven families described with phenotypes overlapping ADTKD and ADPKD. \nSources: Expert list",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:46:01.313628+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALMS1 as ready",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:46:01.301979+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alms1 has been classified as Red List (Low Evidence).",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:45:57.912589+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALMS1 as Red List (low evidence)",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:45:57.900760+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alms1 has been classified as Red List (Low Evidence).",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:45:43.055841+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ALMS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:45:22.145448+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACTN4 as ready",
"entity_name": "ACTN4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:45:22.134247+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actn4 has been classified as Red List (Low Evidence).",
"entity_name": "ACTN4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:45:18.315175+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ACTN4 as Red List (low evidence)",
"entity_name": "ACTN4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:45:18.303699+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actn4 has been classified as Red List (Low Evidence).",
"entity_name": "ACTN4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:45:05.984854+11:00",
"panel_name": "Renal cystic disease_KidGen",
"panel_id": 194,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ACTN4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "ACTN4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:39:48.777811+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_KidGen_VCGS",
"panel_id": 211,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Atypical Haemolytic Uraemic Syndrome_VCGS to Atypical Haemolytic Uraemic Syndrome_KidGen_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-20T15:38:45.313595+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VTN as ready",
"entity_name": "VTN",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:38:45.302153+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vtn has been classified as Amber List (Moderate Evidence).",
"entity_name": "VTN",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:38:35.464348+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: VTN as Amber List (moderate evidence)",
"entity_name": "VTN",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:38:35.442740+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vtn has been classified as Amber List (Moderate Evidence).",
"entity_name": "VTN",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:30:58.388229+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen_VCGS",
"panel_id": 199,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal tubulointerstitial disease_KidGen to Renal tubulointerstitial disease_KidGen_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-20T15:27:13.377590+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAJB11 as ready",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:27:13.366456+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajb11 has been classified as Green List (High Evidence).",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:27:08.666350+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAJB11 as Green List (high evidence)",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:27:08.655474+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajb11 has been classified as Green List (High Evidence).",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:26:51.276537+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DNAJB11 was added\ngene: DNAJB11 was added to Renal tubulointerstitial disease_KidGen. Sources: Expert list\nMode of inheritance for gene: DNAJB11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DNAJB11 were set to 29706351; 29777155\nPhenotypes for gene: DNAJB11 were set to Polycystic kidney disease 6 with or without polycystic liver disease, MIM#618061\nReview for gene: DNAJB11 was set to GREEN\ngene: DNAJB11 was marked as current diagnostic\nAdded comment: At least 7 unrelated families with variants reported in this gene; variable presentation including tubulointerstitial disease (histologically) in addition to polycystic disease (hybrid between PKD and ADTKD). \nSources: Expert list",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:22:06.225190+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP6V0A4 as ready",
"entity_name": "ATP6V0A4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:22:06.213589+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp6v0a4 has been classified as Red List (Low Evidence).",
"entity_name": "ATP6V0A4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:22:01.191214+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATP6V0A4 as Red List (low evidence)",
"entity_name": "ATP6V0A4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:22:01.179488+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp6v0a4 has been classified as Red List (Low Evidence).",
"entity_name": "ATP6V0A4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:21:50.885678+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ATP6V0A4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Renal tubular acidosis, distal, autosomal recessive, MIM#602722; Mode of inheritance: None",
"entity_name": "ATP6V0A4",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:20:11.285683+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AQP2 as ready",
"entity_name": "AQP2",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:20:11.274276+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aqp2 has been classified as Red List (Low Evidence).",
"entity_name": "AQP2",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:20:08.010763+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AQP2 as Red List (low evidence)",
"entity_name": "AQP2",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:20:07.997891+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aqp2 has been classified as Red List (Low Evidence).",
"entity_name": "AQP2",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:19:51.212843+11:00",
"panel_name": "Renal tubulointerstitial disease_KidGen",
"panel_id": 199,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: AQP2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Diabetes insipidus, nephrogenic, MIM#125800; Mode of inheritance: None",
"entity_name": "AQP2",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:01:03.944706+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FBF1 as ready",
"entity_name": "FBF1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:01:03.933498+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fbf1 has been classified as Red List (Low Evidence).",
"entity_name": "FBF1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:00:55.363971+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FBF1 as Red List (low evidence)",
"entity_name": "FBF1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:00:55.351893+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fbf1 has been classified as Red List (Low Evidence).",
"entity_name": "FBF1",
"entity_type": "gene"
},
{
"created": "2019-11-20T15:00:12.569545+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FBF1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "FBF1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:56:14.969750+11:00",
"panel_name": "Overgrowth_VCGS",
"panel_id": 151,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNF135 as ready",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:56:14.958724+11:00",
"panel_name": "Overgrowth_VCGS",
"panel_id": 151,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf135 has been classified as Red List (Low Evidence).",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:56:10.499493+11:00",
"panel_name": "Overgrowth_VCGS",
"panel_id": 151,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RNF135 as Red List (low evidence)",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:56:10.487989+11:00",
"panel_name": "Overgrowth_VCGS",
"panel_id": 151,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf135 has been classified as Red List (Low Evidence).",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:55:24.552643+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNF135 as ready",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:55:24.541562+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf135 has been classified as Red List (Low Evidence).",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:55:16.213637+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RNF135 as Red List (low evidence)",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:55:16.202381+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf135 has been classified as Red List (Low Evidence).",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:54:43.240267+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNF135 as ready",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:54:43.228614+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf135 has been classified as Red List (Low Evidence).",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:54:35.883889+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RNF135 as Red List (low evidence)",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:54:35.872416+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf135 has been classified as Red List (Low Evidence).",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:53:50.276195+11:00",
"panel_name": "Autism_VCGS",
"panel_id": 51,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNF135 as ready",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:53:50.265104+11:00",
"panel_name": "Autism_VCGS",
"panel_id": 51,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf135 has been classified as Red List (Low Evidence).",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:53:46.289980+11:00",
"panel_name": "Autism_VCGS",
"panel_id": 51,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RNF135 as Red List (low evidence)",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:53:46.276847+11:00",
"panel_name": "Autism_VCGS",
"panel_id": 51,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnf135 has been classified as Red List (Low Evidence).",
"entity_name": "RNF135",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:42:12.191006+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMC1 as ready",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:42:12.179505+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc1 has been classified as Red List (Low Evidence).",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:42:03.611638+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LAMC1 as Red List (low evidence)",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:42:03.600575+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc1 has been classified as Red List (Low Evidence).",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:41:44.263582+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAMC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:41:08.298988+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMC1 as ready",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:41:08.287815+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc1 has been classified as Red List (Low Evidence).",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:41:03.851042+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LAMC1 as Red List (low evidence)",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:41:03.839437+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc1 has been classified as Red List (Low Evidence).",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:40:28.671517+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAMC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:39:49.705563+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMC1 as ready",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:39:49.694384+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc1 has been classified as Red List (Low Evidence).",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:39:43.622635+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LAMC1 as Red List (low evidence)",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:39:43.605557+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc1 has been classified as Red List (Low Evidence).",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:39:14.036444+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAMC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "LAMC1",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:35:55.463110+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HCN2 as ready",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:35:55.450932+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hcn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:35:44.749220+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HCN2 as Amber List (moderate evidence)",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:35:44.736894+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hcn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:33:11.368247+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HCN2 as ready",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:33:11.357038+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hcn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:33:05.737008+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HCN2 as Amber List (moderate evidence)",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:33:05.725154+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hcn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:32:36.751531+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HCN2: Rating: AMBER; Mode of pathogenicity: None; Publications: 22131395, 30986657; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HCN2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:24:57.175462+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B3GNT2 as ready",
"entity_name": "B3GNT2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:24:57.164181+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b3gnt2 has been classified as Red List (Low Evidence).",
"entity_name": "B3GNT2",
"entity_type": "gene"
},
{
"created": "2019-11-20T14:24:53.129830+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: B3GNT2 as Red List (low evidence)",
"entity_name": "B3GNT2",
"entity_type": "gene"
}
]
}