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{
"count": 221415,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=367",
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"results": [
{
"created": "2024-10-10T17:56:20.838594+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.286",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: UFC1: Changed phenotypes: Neurodevelopmental disorder with spasticity and poor growth (MIM#618076)",
"entity_name": "UFC1",
"entity_type": "gene"
},
{
"created": "2024-10-10T17:56:14.839615+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.286",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UFC1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UFC1",
"entity_type": "gene"
},
{
"created": "2024-10-10T17:55:55.178756+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2063",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag deep intronic tag was added to gene: UFC1.",
"entity_name": "UFC1",
"entity_type": "gene"
},
{
"created": "2024-10-10T17:55:39.590264+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2063",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UFC1: Rating: GREEN; 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": "2024-10-10T11:49:57.538279+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.390",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: CLPB: Rating: GREEN; Mode of pathogenicity: None; Publications: 34140661; Phenotypes: 3-methylglutaconic aciduria, type VIIB, autosomal recessive (MIM#616271); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CLPB",
"entity_type": "gene"
},
{
"created": "2024-10-10T08:53:27.850304+11:00",
"panel_name": "Motor Neurone Disease",
"panel_id": 25,
"panel_version": "1.24",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: SOD1.",
"entity_name": "SOD1",
"entity_type": "gene"
},
{
"created": "2024-10-09T19:02:33.761018+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS6KA3 as ready",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2024-10-09T19:02:33.739021+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps6ka3 has been classified as Green List (High Evidence).",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2024-10-09T19:02:26.551443+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS6KA3 were changed from to Coffin-Lowry syndrome MIM# 303600",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2024-10-09T19:01:46.630142+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6488",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS6KA3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2024-10-09T19:01:09.959303+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RPS6KA3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Coffin-Lowry syndrome MIM# 303600; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2024-10-09T19:00:11.475128+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPGRIP1L as ready",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2024-10-09T19:00:11.433806+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rpgrip1l has been classified as Green List (High Evidence).",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2024-10-09T19:00:04.196273+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPGRIP1L were changed from to Joubert syndrome 7, MIM# 611560; Meckel syndrome 5, MIM# 611561",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:59:22.508589+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPGRIP1L was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:58:44.250986+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RPGRIP1L: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Joubert syndrome 7, MIM# 611560, Meckel syndrome 5, MIM# 611561; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:54:42.630009+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNASET2 as ready",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:54:42.610123+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnaset2 has been classified as Green List (High Evidence).",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:54:36.990678+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNASET2 were changed from to Leukoencephalopathy, cystic, without megalencephaly, MIM# 612951",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:53:49.292574+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RNASET2 were set to ",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:53:10.571540+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RNASET2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:49:10.187193+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: RNASET2: Added comment: More than 10 families reported, DD/ID is part of the phenotype.; Changed publications: 31349848, 19525954, 27091087, 29336640, 18545798, 15851732",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:48:15.938084+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RNASET2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy, cystic, without megalencephaly, MIM# 612951; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:47:31.745402+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNASEH2C as ready",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:47:31.731837+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnaseh2c has been classified as Green List (High Evidence).",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:47:22.955586+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNASEH2C were changed from to Aicardi-Goutieres syndrome 3, MIM# 610329",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:46:00.245606+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RNASEH2C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:45:11.316667+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6480",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RNASEH2C: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aicardi-Goutieres syndrome 3, MIM# 610329; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:44:21.787783+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6480",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNASEH2B as ready",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:44:21.770988+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6480",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnaseh2b has been classified as Green List (High Evidence).",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:44:04.558415+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6480",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNASEH2B were changed from to Aicardi-Goutieres syndrome 2, MIM# 610181",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:43:21.187258+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6479",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RNASEH2B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:42:42.506152+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6478",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RNASEH2B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aicardi-Goutieres syndrome 2, MIM# 610181; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:41:35.690062+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6478",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNASEH2A as ready",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:41:35.676210+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6478",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnaseh2a has been classified as Green List (High Evidence).",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:33:20.251329+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6478",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNASEH2A were changed from to Aicardi-Goutieres syndrome 4, MIM# 610333",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:32:41.519868+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6477",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RNASEH2A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:32:03.516044+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6476",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RNASEH2A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aicardi-Goutieres syndrome 4, MIM# 610333; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:31:15.389152+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6476",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RMND1 as ready",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:31:15.355367+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6476",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rmnd1 has been classified as Green List (High Evidence).",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:31:10.745821+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6476",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RMND1 were changed from to Combined oxidative phosphorylation deficiency 11 MIM#614922",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:30:31.505435+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6475",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RMND1 were set to ",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:29:53.678509+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6474",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RMND1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:29:19.571437+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RMND1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Combined oxidative phosphorylation deficiency 11 MIM#614922; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:28:27.213338+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RIT1 as ready",
"entity_name": "RIT1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:28:27.196527+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rit1 has been classified as Green List (High Evidence).",
"entity_name": "RIT1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:28:12.201456+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RIT1 were changed from to Noonan syndrome 8, MIM# 615355",
"entity_name": "RIT1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:27:13.230937+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6472",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RIT1 were set to ",
"entity_name": "RIT1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:26:26.774310+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: RIT1 was changed from to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
"entity_name": "RIT1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:25:52.214217+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6470",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RIT1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RIT1",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:24:55.062176+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RFC4 as ready",
"entity_name": "RFC4",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:24:55.045178+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rfc4 has been classified as Green List (High Evidence).",
"entity_name": "RFC4",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:24:50.582040+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RFC4 were changed from RFC4-related multisystem disorder to Neurodevelopmental disorder, MONDO:0700092, RFC4-related",
"entity_name": "RFC4",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:24:03.128068+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RFC4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder, MONDO:0700092, RFC4-related; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RFC4",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:21:11.884231+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RARS2 as ready",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:21:11.871737+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rars2 has been classified as Green List (High Evidence).",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:17:05.091089+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RARS2 were changed from to Pontocerebellar hypoplasia, type 6, MIM# 611523",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:13:55.480424+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6467",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RARS2 were set to ",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:07:48.321977+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6466",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2024-10-09T18:07:00.545391+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6465",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RARS2: Rating: GREEN; Mode of pathogenicity: None; Publications: 17847012, 20635367, 25809939; Phenotypes: Pontocerebellar hypoplasia, type 6, MIM# 611523; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:42:18.475432+11:00",
"panel_name": "Parathyroid Cancer",
"panel_id": 4363,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2024-10-09T14:42:09.479049+11:00",
"panel_name": "Parathyroid Cancer",
"panel_id": 4363,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel status changed from internal to public",
"entity_name": null,
"entity_type": null
},
{
"created": "2024-10-09T14:41:47.712001+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2024-10-09T14:41:05.495421+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel status changed from internal to public",
"entity_name": null,
"entity_type": null
},
{
"created": "2024-10-09T14:40:54.248646+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHD as ready",
"entity_name": "SDHD",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:40:54.232087+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhd has been classified as Green List (High Evidence).",
"entity_name": "SDHD",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:40:47.473434+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHC as ready",
"entity_name": "SDHC",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:40:47.459963+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhc has been classified as Green List (High Evidence).",
"entity_name": "SDHC",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:39:51.171703+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHB as ready",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:39:51.152083+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhb has been classified as Green List (High Evidence).",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:38:53.178502+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHA as ready",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:38:53.164955+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdha has been classified as Green List (High Evidence).",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:35:47.422127+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKAR1A as ready",
"entity_name": "PRKAR1A",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:35:47.406657+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkar1a has been classified as Green List (High Evidence).",
"entity_name": "PRKAR1A",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:35:41.331991+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MEN1 as ready",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:35:41.320255+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: men1 has been classified as Green List (High Evidence).",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:35:34.842688+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDKN1B as ready",
"entity_name": "CDKN1B",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:35:34.826366+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdkn1b has been classified as Green List (High Evidence).",
"entity_name": "CDKN1B",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:35:25.671036+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AIP as ready",
"entity_name": "AIP",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:35:25.651308+11:00",
"panel_name": "Pituitary Tumour",
"panel_id": 4364,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aip has been classified as Green List (High Evidence).",
"entity_name": "AIP",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:59.346185+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2024-10-09T14:34:41.613161+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel status changed from internal to public",
"entity_name": null,
"entity_type": null
},
{
"created": "2024-10-09T14:34:29.062258+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TP53 as ready",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:29.038159+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tp53 has been classified as Green List (High Evidence).",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:21.256572+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PMS2 as ready",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:21.236306+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pms2 has been classified as Green List (High Evidence).",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:15.439584+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PALB2 as ready",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:15.405267+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: palb2 has been classified as Green List (High Evidence).",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:08.382296+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MSH6 as ready",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:08.355432+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: msh6 has been classified as Green List (High Evidence).",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:02.436594+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MSH2 as ready",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:34:02.410361+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: msh2 has been classified as Green List (High Evidence).",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:33:56.839900+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MLH1 as ready",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:33:56.820906+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlh1 has been classified as Green List (High Evidence).",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:33:47.086821+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HOXB13 as ready",
"entity_name": "HOXB13",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:33:47.063662+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hoxb13 has been classified as Green List (High Evidence).",
"entity_name": "HOXB13",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:33:40.226883+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EPCAM as ready",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:33:40.210951+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: epcam has been classified as Green List (High Evidence).",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:33:34.108632+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHEK2 as ready",
"entity_name": "CHEK2",
"entity_type": "gene"
},
{
"created": "2024-10-09T14:33:34.084663+11:00",
"panel_name": "Prostate Cancer",
"panel_id": 4372,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chek2 has been classified as Green List (High Evidence).",
"entity_name": "CHEK2",
"entity_type": "gene"
}
]
}