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{
"created": "2021-06-26T12:52:53.294479+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.315",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: BBS7: Changed phenotypes: Bardet-Biedl syndrome 7, MIM# 615984, MONDO:0014435",
"entity_name": "BBS7",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:51:53.794183+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS5 as ready",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:51:53.784225+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs5 has been classified as Green List (High Evidence).",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:51:50.872873+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS5 were changed from to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:51:26.626807+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.203",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS5 were set to ",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:50:52.641130+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, polydactyly is a feature.",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:50:29.616200+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, renal abnormalities are a feature.",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:49:53.226085+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS5 as ready",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:49:53.216792+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs5 has been classified as Green List (High Evidence).",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:49:50.578297+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS5 were changed from to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:49:27.624760+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS5 were set to ",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:48:58.018930+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:48:33.885650+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BBS5: Rating: GREEN; Mode of pathogenicity: None; Publications: 19252258, 15137946, 10053027, 15637713; Phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:48:01.122168+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3901",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS5 as ready",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:48:01.112669+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3901",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs5 has been classified as Green List (High Evidence).",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:47:57.447056+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3901",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS5 were changed from to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:47:33.180564+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3900",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS5 were set to ",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:47:00.278717+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3899",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-26T12:46:19.918474+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3898",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BBS5: Rating: GREEN; Mode of pathogenicity: None; Publications: 19252258, 15137946, 10053027, 15637713; Phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:27:02.612905+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS5 as ready",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:27:02.603359+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs5 has been classified as Green List (High Evidence).",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:26:55.238138+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS5 were changed from to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:26:35.555556+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS5 were set to ",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:26:15.228631+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:25:57.587276+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BBS5: Rating: GREEN; Mode of pathogenicity: None; Publications: 19252258, 15137946, 10053027, 15637713; Phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:25:12.299122+10:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "1.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS5 were changed from Bardet-Biedl syndrome 5, MIM#615983 to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:24:38.809605+10:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "1.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: BBS5: Changed phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:24:12.181815+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.315",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS5 as ready",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:24:12.168140+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.315",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs5 has been classified as Green List (High Evidence).",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:24:08.288554+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.315",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS5 were changed from to Bardet-Biedl syndrome 5, MIM#615983; MONDO:0014434",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:23:38.574462+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS5 were set to ",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:23:02.384181+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:22:32.277268+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.312",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: BBS5: Changed phenotypes: Bardet-Biedl syndrome 5, MIM#615983, MONDO:0014434",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:17:38.946428+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3898",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS4 as ready",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:17:38.932992+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3898",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs4 has been classified as Green List (High Evidence).",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:17:34.318467+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3898",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS4 were changed from to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:17:06.614350+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3897",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS4 were set to ",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:16:45.886552+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3896",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:15:45.308510+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3895",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BBS4: Rating: GREEN; Mode of pathogenicity: None; Publications: 12016587, 11381270; Phenotypes: Bardet-Biedl syndrome 4, MIM#615982, MONDO:0014433; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:14:58.093857+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS4 as ready",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:14:58.081528+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs4 has been classified as Green List (High Evidence).",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:14:55.420478+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS4 were changed from to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:14:26.913899+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS4 were set to ",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:14:07.979234+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:13:36.268612+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BBS4: Rating: GREEN; Mode of pathogenicity: None; Publications: 12016587, 11381270; Phenotypes: Bardet-Biedl syndrome 4, MIM#615982, MONDO:0014433; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:12:23.236428+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS4 as ready",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:12:23.226628+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs4 has been classified as Green List (High Evidence).",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:12:11.701183+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS4 were changed from to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:11:34.496145+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS4 were set to ",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:01:33.958918+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS4 as ready",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:01:33.947881+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs4 has been classified as Green List (High Evidence).",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:00:40.056290+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS4 were changed from to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T19:00:16.857119+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS4 were set to ",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:59:55.294109+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:59:35.751701+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BBS4: Rating: GREEN; Mode of pathogenicity: None; Publications: 12016587, 11381270; Phenotypes: Bardet-Biedl syndrome 4, MIM#615982, MONDO:0014433; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:58:57.280529+10:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "1.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS4 were changed from Bardet-Biedl syndrome 4, MIM#615982 to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:58:13.084203+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.312",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS4 as ready",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:58:13.073724+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.312",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs4 has been classified as Green List (High Evidence).",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:58:08.991501+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.312",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS4 were changed from to Bardet-Biedl syndrome 4, MIM#615982; MONDO:0014433",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:57:38.816260+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.311",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS4 were set to ",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:57:10.127729+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.310",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T18:56:41.057181+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: BBS4: Changed phenotypes: Bardet-Biedl syndrome 4, MIM#615982, MONDO:0014433",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:59:31.004429+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS2 as ready",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:59:30.991365+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs2 has been classified as Green List (High Evidence).",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:58:53.625640+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS2 were changed from to Bardet-Biedl syndrome 2, MIM# 615981; Retinitis pigmentosa 74, MIM# 616562",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:56:45.159558+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.308",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS2 were set to ",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:56:18.682367+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:55:49.202417+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Well established gene-disease association.; to: Well established gene-disease association. Limited number of families also reported with isolated RP.",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:55:32.910643+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: BBS2: Changed publications: 11567139, 16823392, 28143435, 31960602, 25541840; Changed phenotypes: Bardet-Biedl syndrome 2, MIM# 615981, Retinitis pigmentosa 74, MIM# 616562",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:53:27.948690+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS12 as ready",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:53:27.936812+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs12 has been classified as Green List (High Evidence).",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:52:57.414853+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS12 were changed from to Bardet-Biedl syndrome 12, MIM# 615989",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:52:33.171996+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.305",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS12 were set to ",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:52:04.198951+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.304",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:51:26.797193+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARL6 as ready",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T17:51:26.787083+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arl6 has been classified as Green List (High Evidence).",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T15:04:22.591586+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS10 as ready",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2021-06-25T15:04:22.580527+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs10 has been classified as Green List (High Evidence).",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:55:39.108966+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS10 were changed from to Bardet-Biedl syndrome 10, MIM# 615987",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:55:14.508417+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS10 were set to ",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:54:43.100416+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.301",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:54:06.236747+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS1 as ready",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:54:06.224602+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs1 has been classified as Green List (High Evidence).",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:54:02.500805+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS1 were changed from to Bardet-Biedl syndrome 1, MIM# 209900",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:53:29.342336+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.299",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS1 were set to ",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:52:25.727303+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.298",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:51:41.484879+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.297",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B9D2 as ready",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:51:41.470288+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.297",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b9d2 has been classified as Green List (High Evidence).",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:51:38.472541+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.297",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B9D2 were changed from to Joubert syndrome 34, MIM# 614175; Meckel syndrome 10, MIM# 614175",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:51:08.399371+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.296",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: B9D2 were set to ",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:50:51.125877+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.295",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: B9D2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:48:15.960626+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARL6 as ready",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:48:15.950014+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arl6 has been classified as Green List (High Evidence).",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:48:13.581956+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ARL6 were changed from to Bardet-Biedl syndrome 3, MIM# 600151",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:47:42.437173+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.155",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ARL6 were set to ",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:47:13.282090+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ARL6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:46:40.658245+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ARL6: Rating: GREEN; Mode of pathogenicity: None; Publications: 15258860, 32361989, 31888296, 25402481; Phenotypes: Bardet-Biedl syndrome 3, MIM# 600151; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:42:14.292851+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3895",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARL6 as ready",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:42:14.282296+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3895",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arl6 has been classified as Green List (High Evidence).",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2021-06-25T14:42:10.057183+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3895",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ARL6 were changed from to Bardet-Biedl syndrome 3, MIM# 600151",
"entity_name": "ARL6",
"entity_type": "gene"
}
]
}