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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1138",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1136",
"results": [
{
"created": "2021-11-08T20:24:45.504264+11:00",
"panel_name": "Periventricular Grey Matter Heterotopia",
"panel_id": 19,
"panel_version": "1.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HNRNPK as Green List (high evidence)",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:24:45.494504+11:00",
"panel_name": "Periventricular Grey Matter Heterotopia",
"panel_id": 19,
"panel_version": "1.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpk has been classified as Green List (High Evidence).",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:24:13.599492+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HNRNPK as ready",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:24:13.589957+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpk has been classified as Green List (High Evidence).",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:24:06.138779+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HNRNPK as Green List (high evidence)",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:24:06.128456+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpk has been classified as Green List (High Evidence).",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:23:34.932658+11:00",
"panel_name": "Clefting disorders",
"panel_id": 3368,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HNRNPK as ready",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:23:34.921669+11:00",
"panel_name": "Clefting disorders",
"panel_id": 3368,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpk has been classified as Green List (High Evidence).",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:23:30.467392+11:00",
"panel_name": "Clefting disorders",
"panel_id": 3368,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HNRNPK as Green List (high evidence)",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:23:30.456746+11:00",
"panel_name": "Clefting disorders",
"panel_id": 3368,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpk has been classified as Green List (High Evidence).",
"entity_name": "HNRNPK",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:23:03.296059+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HES7 as ready",
"entity_name": "HES7",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:23:03.285877+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hes7 has been classified as Green List (High Evidence).",
"entity_name": "HES7",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:22:54.711573+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HES7 were changed from to Spondylocostal dysostosis 4, autosomal recessive MIM#613686",
"entity_name": "HES7",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:22:32.208206+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9651",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HES7 were set to ",
"entity_name": "HES7",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:22:15.458206+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9650",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HES7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HES7",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:21:14.128603+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9649",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DIS3L2 as ready",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:21:14.115025+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9649",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dis3l2 has been classified as Green List (High Evidence).",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:21:06.685791+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9649",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DIS3L2 were changed from to Perlman syndrome MIM# 267000",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:20:48.901945+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DIS3L2 were set to ",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:20:29.728551+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9647",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DIS3L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:20:12.931993+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DIS3L2: Rating: GREEN; Mode of pathogenicity: None; Publications: 22306653, 28328139, 29950491; Phenotypes: Perlman syndrome MIM# 267000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:18:56.697564+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.271",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DIS3L2 as ready",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:18:56.687951+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.271",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dis3l2 has been classified as Green List (High Evidence).",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:18:51.949125+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.271",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DIS3L2 were changed from PERLMAN SYNDROME to Perlman syndrome MIM# 267000",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:18:39.339044+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.270",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DIS3L2 were set to ",
"entity_name": "DIS3L2",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:17:52.511548+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DHODH as ready",
"entity_name": "DHODH",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:17:52.501266+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dhodh has been classified as Green List (High Evidence).",
"entity_name": "DHODH",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:17:48.649973+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DHODH were changed from POSTAXIAL ACROFACIAL DYSOSTOSIS to Miller syndrome, MIM# 263750",
"entity_name": "DHODH",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:17:15.718186+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DHODH were set to ",
"entity_name": "DHODH",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:16:35.823174+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDX3X as ready",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:16:35.813698+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddx3x has been classified as Green List (High Evidence).",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:16:32.177439+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDX3X were changed from to Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:15:56.594250+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DDX3X were set to ",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:15:04.286830+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DDX3X was changed from X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:14:47.471151+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DDX3X was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:14:25.141977+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDX3X as ready",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:14:25.131405+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddx3x has been classified as Green List (High Evidence).",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:14:08.184486+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4259",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DDX3X: Rating: GREEN; Mode of pathogenicity: None; Publications: 30266093, 26235985, 25533962, 33528536, 30936465, 31274575, 30817323; Phenotypes: Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:14:00.570295+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDX3X were changed from to Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:13:41.720874+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9645",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DDX3X were set to ",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:13:22.533740+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9644",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DDX3X was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:12:53.634744+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DDX3X: Rating: GREEN; Mode of pathogenicity: None; Publications: 30266093, 26235985, 25533962, 33528536, 30936465, 31274575, 30817323; Phenotypes: Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:11:29.727519+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDX3X as ready",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:11:29.717417+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddx3x has been classified as Green List (High Evidence).",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:11:25.979173+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDX3X were changed from Intellectual disability; INTELLECTUAL DIABILITY; Mental retardation, X-linked 102, 300958 to Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:11:13.183270+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DDX3X were set to 30266093; 26235985; 25533962",
"entity_name": "DDX3X",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:08:03.191991+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATAD1 as ready",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:08:03.181472+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atad1 has been classified as Green List (High Evidence).",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:07:30.625667+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATAD1 as Green List (high evidence)",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:07:30.614475+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atad1 has been classified as Green List (High Evidence).",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:07:14.523557+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ATAD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hyperekplexia 4 - #618011; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:05:22.526332+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: HSPD1: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:05:13.580689+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSPD1 as ready",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:05:13.571144+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hspd1 has been classified as Green List (High Evidence).",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:05:09.543849+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HSPD1 were changed from LEUKODYSTROPHY HYPOMYELINATING TYPE 4 to Leukodystrophy, hypomyelinating, 4, MIM# 612233",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:04:57.528508+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HSPD1 were set to ",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:04:45.237181+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HSPD1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:04:21.137784+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HSPD1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:04:07.137634+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HSPD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:02:45.193940+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADCY6 were changed from Lethal congenital contracture syndrome 8, MIM#616287 to Lethal congenital contracture syndrome 8, MIM#616287; MONDO:0014570",
"entity_name": "ADCY6",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:01:54.179023+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.259",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADCY6 as ready",
"entity_name": "ADCY6",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:01:54.165064+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.259",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adcy6 has been classified as Green List (High Evidence).",
"entity_name": "ADCY6",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:01:50.599275+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.259",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADCY6 were changed from Lethal congenital contracture syndrome 8 - #616287 to Lethal congenital contracture syndrome 8, MIM#616287",
"entity_name": "ADCY6",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:01:35.770528+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.258",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ADCY6 were set to 24319099, 26257172, 31846058; 33820833",
"entity_name": "ADCY6",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:01:21.351187+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.257",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ADCY6 as Green List (high evidence)",
"entity_name": "ADCY6",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:01:21.341918+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.257",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adcy6 has been classified as Green List (High Evidence).",
"entity_name": "ADCY6",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:00:24.512252+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SIK3 as ready",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:00:24.499214+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sik3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:00:14.413908+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SIK3 as Amber List (moderate evidence)",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T20:00:14.402148+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sik3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:59:55.781614+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SIK3: Rating: AMBER; Mode of pathogenicity: None; Publications: 30232230, 22318228; Phenotypes: Spondyloepimetaphyseal dysplasia, Krakow type - #618162; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:58:52.176992+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SIK3 as ready",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:58:52.166263+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sik3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:58:44.202462+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SIK3 were changed from ?Spondyloepimetaphyseal dysplasia, Krakow type - #618162 to Spondyloepimetaphyseal dysplasia, Krakow type - #618162",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:58:22.755541+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SIK3 as Amber List (moderate evidence)",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:58:22.745515+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sik3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:57:55.130018+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SIK3 as ready",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:57:55.118697+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sik3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:57:52.134906+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SIK3 were changed from ?Spondyloepimetaphyseal dysplasia, Krakow type - #618162 to Spondyloepimetaphyseal dysplasia, Krakow type - #618162",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:57:25.952858+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SIK3 as Amber List (moderate evidence)",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:57:25.943321+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sik3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SIK3",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:56:24.791449+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LIPA as ready",
"entity_name": "LIPA",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:56:24.780744+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lipa has been classified as Green List (High Evidence).",
"entity_name": "LIPA",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:56:20.108432+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LIPA were set to 12666227",
"entity_name": "LIPA",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:56:00.682773+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LIPA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Wolman disease, MIM# 278000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LIPA",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:01:06.913270+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DCHS1 as ready",
"entity_name": "DCHS1",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:01:06.902198+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dchs1 has been classified as Green List (High Evidence).",
"entity_name": "DCHS1",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:01:02.457232+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DCHS1 were changed from PERIVENTRICULAR NEURONAL HETEROTOPIA to Van Maldergem syndrome 1, MIM# 601390",
"entity_name": "DCHS1",
"entity_type": "gene"
},
{
"created": "2021-11-08T19:00:49.550592+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.253",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DCHS1 were set to ",
"entity_name": "DCHS1",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:59:34.507885+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.252",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSF4 as ready",
"entity_name": "HSF4",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:59:34.497627+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.252",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hsf4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HSF4",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:59:31.207087+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.252",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HSF4 were changed from CATARACT ZONULAR HSF4-RELATED; CATARACT MARNER TYPE to Cataract 5, multiple types MIM#116800",
"entity_name": "HSF4",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:59:14.890852+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.251",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HSF4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HSF4",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:59:01.001736+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HSF4 as Amber List (moderate evidence)",
"entity_name": "HSF4",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:59:00.991603+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hsf4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "HSF4",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:57:46.171778+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSD17B3 as ready",
"entity_name": "HSD17B3",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:57:46.161739+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hsd17b3 has been classified as Green List (High Evidence).",
"entity_name": "HSD17B3",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:57:43.396398+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HSD17B3 were changed from to Pseudohermaphroditism, male, with gynecomastia MIM#264300",
"entity_name": "HSD17B3",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:57:18.840488+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HSD17B3 were set to ",
"entity_name": "HSD17B3",
"entity_type": "gene"
},
{
"created": "2021-11-08T18:56:43.913327+11:00",
"panel_name": "Differences of Sex Development",
"panel_id": 99,
"panel_version": "0.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HSD17B3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HSD17B3",
"entity_type": "gene"
}
]
}