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"user_name": "Zornitza Stark",
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"text": "Publications for gene: PDE6D were set to 24166846; 30423442",
"entity_name": "PDE6D",
"entity_type": "gene"
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{
"created": "2020-01-03T20:14:22.579362+11:00",
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"panel_id": 159,
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"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on publications: Second family identified",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:14:22.547601+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:13:56.407152+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Amber List (moderate evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:13:56.347761+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:13:10.712010+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
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"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE6D as ready",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:13:10.706348+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Second family identified PMID 30423442",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:13:10.676165+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:12:07.816846+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:11:37.553715+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Amber List (moderate evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:11:37.542419+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:11:19.114090+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846; 30423442",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:11:03.680092+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1475",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Amber List (moderate evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:11:03.663661+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1475",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:10:52.364113+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Amber List (moderate evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:10:52.345867+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:10:24.330366+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Amber List (moderate evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:10:24.266607+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:09:32.690094+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:09:27.618311+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE6D as ready",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:09:27.611451+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Second family identified in the literature.",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:09:27.578802+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:09:21.460880+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:08:57.511939+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Amber List (moderate evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:08:57.467156+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:08:31.379089+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846; 30423442",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:08:16.600273+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE6D as ready",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:08:16.587923+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:07:54.724832+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:07:48.442025+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE6D as ready",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:07:48.435959+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Two families; link with regression not established.",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:07:48.378625+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:07:17.497552+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.587",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:07:00.838332+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Amber List (moderate evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:07:00.822247+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:06:20.068028+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1474",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PDE6D: Changed rating: AMBER",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:06:06.840930+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from Joubert syndrome 22, OMIM #615665 to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
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"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE6D as ready",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:05:29.795395+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:05:28.416005+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from Joubert syndrome 22, OMIM #615665 to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:05:19.662896+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:04:53.408058+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:04:39.633766+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.585",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:04:27.839891+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to ",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:04:13.998503+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to ",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:03:45.242198+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:03:19.652414+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Red List (low evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:03:19.591612+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:02:20.867957+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE6D as ready",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:02:20.851265+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:02:20.448234+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to ",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:02:13.064169+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to 24166846",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:02:13.063390+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:01:26.769244+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to ",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:01:21.866495+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:00:25.865029+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.583",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:00:08.689367+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Red List (low evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:00:08.675659+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:59:53.625049+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:59:47.551738+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:58:58.082238+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:58:38.997727+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Red List (low evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:58:38.967730+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:58:25.602652+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Red List (low evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:58:25.589337+11:00",
"panel_name": "Joubert syndrome and other cerebellar malformations_VCGS",
"panel_id": 129,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:57:50.508358+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:56:59.536070+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": "reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:56:48.874163+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE6D as ready",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:56:48.862406+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:56:23.800495+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:55:51.699928+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to ",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:54:08.393982+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:53:38.967554+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDE6D as Red List (low evidence)",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:53:38.955368+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:53:06.162299+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PDE6D: Rating: RED; Mode of pathogenicity: None; Publications: 24166846; Phenotypes: Joubert syndrome 22, OMIM #615665; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:49:56.964064+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC41A1 as ready",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:49:56.951908+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc41a1 has been classified as Red List (Low Evidence).",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:49:48.211544+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC41A1 were changed from to Nephronophthisis",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:49:38.261445+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.580",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC41A1 were set to ",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:49:29.771444+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC41A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:49:07.436047+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.578",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC41A1 as Red List (low evidence)",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:49:07.424905+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.578",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc41a1 has been classified as Red List (Low Evidence).",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:48:45.296036+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.577",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC41A1: Rating: RED; Mode of pathogenicity: None; Publications: 23661805; Phenotypes: Nephronophthisis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:45:39.213087+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1474",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIM32 as ready",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:45:39.202364+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1474",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:45:34.565582+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1474",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM32 were changed from to Bardet-Biedl syndrome 11, MIM# 615988",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:45:23.977990+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1473",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIM32 were set to ",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:45:14.092541+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1472",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIM32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:45:06.595035+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIM32 as Red List (low evidence)",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:45:06.582888+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:44:53.030876+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1470",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: None; Publications: 16606853; Phenotypes: Bardet-Biedl syndrome 11, MIM# 615988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:43:34.203041+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM32 were changed from Bardet-Biedl syndrome 11, MIM# 615988 to Bardet-Biedl syndrome 11, MIM# 615988",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:43:23.154058+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIM32 as ready",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:43:23.141433+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:43:08.299582+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIM32 were set to 16606853",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:42:42.330453+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM32 were changed from to Bardet-Biedl syndrome 11, MIM# 615988",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:42:16.331642+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIM32 were set to ",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:41:50.522436+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIM32 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:41:24.475911+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIM32 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:40:58.515644+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIM32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
}
]
}