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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=221",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=219",
"results": [
{
"created": "2025-05-27T20:04:50.240590+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SERPINH1 as ready",
"entity_name": "SERPINH1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:04:50.233149+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: serpinh1 has been classified as Green List (High Evidence).",
"entity_name": "SERPINH1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:04:45.301978+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SERPINH1 were changed from Orofaciodigital syndrome VI, 277170 (3) to Osteogenesis imperfecta, type X, MIM# 613848; Osteogenesis imperfecta type 10, MONDO:0013459",
"entity_name": "SERPINH1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:04:34.285941+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1024",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SERPINH1 were set to ",
"entity_name": "SERPINH1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:02:00.996539+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SERAC1 as ready",
"entity_name": "SERAC1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:02:00.989053+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: serac1 has been classified as Green List (High Evidence).",
"entity_name": "SERAC1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:01:55.283725+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SERAC1 were changed from 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, 614739 (3) to 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, MIM# 614739",
"entity_name": "SERAC1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:01:35.581259+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1022",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SERAC1 were set to ",
"entity_name": "SERAC1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:01:06.674459+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1021",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SEPSECS as ready",
"entity_name": "SEPSECS",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:01:06.667189+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1021",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sepsecs has been classified as Green List (High Evidence).",
"entity_name": "SEPSECS",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:00:59.581012+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1021",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SEPSECS were changed from Pontocerebellar hypoplasia type 2D, 613811 (3) to Pontocerebellar hypoplasia type 2D, MIM# 613811",
"entity_name": "SEPSECS",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:00:47.039126+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1020",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SEPSECS were set to ",
"entity_name": "SEPSECS",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:59:56.378185+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1019",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SEC23B as ready",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:59:56.370984+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1019",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sec23b has been classified as Green List (High Evidence).",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:59:51.674544+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1019",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SEC23B were changed from Dyserythropoietic anemia, congenital, type II, 224100 (3) to Dyserythropoietic anemia, congenital, type II MIM#224100",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:59:39.800157+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1018",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SEC23B were set to ",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:59:04.531795+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1017",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDCCAG8 as ready",
"entity_name": "SDCCAG8",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:59:04.524386+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1017",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdccag8 has been classified as Green List (High Evidence).",
"entity_name": "SDCCAG8",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:58:59.071601+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1017",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SDCCAG8 were changed from Bardet-Biedl syndrome 16, 615993 (3) to Bardet-Biedl syndrome 16 (MIM# 615993); Senior-Loken syndrome 7 (MIM# 613615)",
"entity_name": "SDCCAG8",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:58:44.798808+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SDCCAG8 were set to ",
"entity_name": "SDCCAG8",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:58:20.387647+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1015",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SCO2 as ready",
"entity_name": "SCO2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:58:20.377912+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1015",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sco2 has been classified as Green List (High Evidence).",
"entity_name": "SCO2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:58:15.950462+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1015",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SCO2 were changed from Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, 604377 (3) to Mitochondrial complex IV deficiency, nuclear type 2 MIM#604377",
"entity_name": "SCO2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:55:32.011109+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1014",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SCO2 were set to ",
"entity_name": "SCO2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:55:08.343342+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1013",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SC5D as ready",
"entity_name": "SC5D",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:55:08.336196+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1013",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sc5d has been classified as Green List (High Evidence).",
"entity_name": "SC5D",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:55:04.487029+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1013",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SC5D were changed from Lathosterolosis, 607330 (3) to Lathosterolosis, MIM#607330",
"entity_name": "SC5D",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:54:54.665023+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1012",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SC5D were set to ",
"entity_name": "SC5D",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:54:20.959065+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1011",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SAMHD1 as ready",
"entity_name": "SAMHD1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:54:20.949783+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1011",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: samhd1 has been classified as Green List (High Evidence).",
"entity_name": "SAMHD1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:54:15.984580+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1011",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SAMHD1 were changed from Aicardi-Goutieres syndrome 5, 612952 (3) to Aicardi-Goutieres syndrome 5, MIM# 612952",
"entity_name": "SAMHD1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:53:51.949310+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1010",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SACS as ready",
"entity_name": "SACS",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:53:51.942468+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1010",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sacs has been classified as Green List (High Evidence).",
"entity_name": "SACS",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:53:47.480379+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1010",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SACS were changed from Spastic ataxia, Charlevoix-Saguenay type, 270550 (3) to Spastic ataxia, Charlevoix-Saguenay type, MIM#270550",
"entity_name": "SACS",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:53:35.208749+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1009",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SACS were set to ",
"entity_name": "SACS",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:53:22.541428+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1008",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: SACS.",
"entity_name": "SACS",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:52:53.968895+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1008",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RYR1 as ready",
"entity_name": "RYR1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:52:53.960554+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1008",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ryr1 has been classified as Green List (High Evidence).",
"entity_name": "RYR1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:52:49.886465+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1008",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RYR1 were changed from Central core disease, MIM# 117000; Neuromuscular disease, congenital, with uniform type 1 fiber, MIM# 117000 to Central core disease (MIM#117000); Minicore myopathy with external ophthalmoplegia (MIM#255320); Neuromuscular disease, congenital, with uniform type 1 fiber (MIM#117000)",
"entity_name": "RYR1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:52:05.482888+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1007",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RTEL1 as ready",
"entity_name": "RTEL1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:52:05.476239+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1007",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rtel1 has been classified as Green List (High Evidence).",
"entity_name": "RTEL1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:52:00.686594+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1007",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RTEL1 were changed from Dyskeratosis congenita, autosomal recessive 5, 615190 (3) to Dyskeratosis congenita, autosomal recessive 5, MIM#615190",
"entity_name": "RTEL1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:51:48.710035+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1006",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RTEL1 were set to ",
"entity_name": "RTEL1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:51:23.001388+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1005",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS6KA3 as ready",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:51:22.987831+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1005",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps6ka3 has been classified as Green List (High Evidence).",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:51:04.460684+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1005",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS6KA3 was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:50:53.010517+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1004",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS6KA3 were changed from Coffin-Lowry syndrome to Coffin-Lowry syndrome, MIM#303600; Intellectual developmental disorder, X-linked 19; MIM#300844",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:50:42.699426+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1003",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS6KA3 were set to ",
"entity_name": "RPS6KA3",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:50:19.021019+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPGRIP1L as ready",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:50:19.012911+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rpgrip1l has been classified as Green List (High Evidence).",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:50:14.868018+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPGRIP1L were changed from Meckel syndrome 5, 611561 (3) to Joubert syndrome 7, MIM# 611560; Meckel syndrome 5, MIM# 611561; COACH syndrome 3, MIM# 619113; Ciliopathy, RPGRIP1L-related, MONDO:0005308",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:50:02.171738+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1001",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPGRIP1L were set to ",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:49:37.192047+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPE65 as ready",
"entity_name": "RPE65",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:49:37.182728+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rpe65 has been classified as Green List (High Evidence).",
"entity_name": "RPE65",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:49:31.350388+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPE65 were changed from Leber congenital amaurosis 2, 204100 (3) to Retinitis pigmentosa 20, MIM#613794; Leber congenital amaurosis 2, MIM#204100",
"entity_name": "RPE65",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:49:05.807761+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RP2 as ready",
"entity_name": "RP2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:49:05.792309+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rp2 has been classified as Green List (High Evidence).",
"entity_name": "RP2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:47:36.692846+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RP2 were changed from Retinitis pigmentosa 2, 312600 (3) to Retinitis pigmentosa 2, MIM #312600",
"entity_name": "RP2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:47:25.950177+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.998",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RP2 were set to ",
"entity_name": "RP2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:46:57.443436+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.997",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNASEH2C as ready",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:46:57.436153+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.997",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnaseh2c has been classified as Green List (High Evidence).",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:46:53.253847+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.997",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNASEH2C were changed from Aicardi-Goutieres syndrome 3, 610329 (3) to Aicardi-Goutieres syndrome 3, MIM# 610329",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:46:36.602145+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RNASEH2C were set to ",
"entity_name": "RNASEH2C",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:46:12.837278+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.995",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNASEH2B as ready",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:46:12.827921+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.995",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnaseh2b has been classified as Green List (High Evidence).",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:46:09.026025+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.995",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNASEH2B were changed from Aicardi-Goutieres syndrome 2, 610181 (3) to Aicardi-Goutieres syndrome 2 MIM#610181",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:45:58.195239+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.994",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RNASEH2B were set to ",
"entity_name": "RNASEH2B",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:45:24.050954+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNASEH2A as ready",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:45:24.044094+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnaseh2a has been classified as Green List (High Evidence).",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:45:16.703971+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RNASEH2A were changed from Aicardi-Goutieres syndrome 4, 610333 (3) to Aicardi-Goutieres syndrome 4 MIM#610333; RNASEH2A-related type 1 interferonopathy MONDO:0700259",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:45:07.109796+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.992",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RNASEH2A were set to ",
"entity_name": "RNASEH2A",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:44:27.058788+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.991",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RMRP as ready",
"entity_name": "RMRP",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:44:27.051743+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.991",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rmrp has been classified as Green List (High Evidence).",
"entity_name": "RMRP",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:44:18.826978+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.991",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RMRP were changed from Cartilage-hair hypoplasia, 250250 (3) to Cartilage-hair hypoplasia MIM#250250; Anauxetic dysplasia 1, MIM#607095; Metaphyseal dysplasia without hypotrichosis MIM#250460",
"entity_name": "RMRP",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:44:06.077551+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RMRP were set to ",
"entity_name": "RMRP",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:43:23.533197+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.989",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RMND1 as ready",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:43:23.523598+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.989",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rmnd1 has been classified as Green List (High Evidence).",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:43:17.019149+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.989",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RMND1 were changed from Combined oxidative phosphorylation deficiency 11, 614922 (3) to Combined oxidative phosphorylation deficiency 11, MIM#614922",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:43:06.205934+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.988",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RMND1 were set to ",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:42:40.827456+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RDH12 as ready",
"entity_name": "RDH12",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:42:40.817606+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rdh12 has been classified as Green List (High Evidence).",
"entity_name": "RDH12",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:42:35.015228+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RDH12 were changed from Leber congenital amaurosis 13, 612712 (3) to Leber congenital amaurosis 13, MIM#612712",
"entity_name": "RDH12",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:42:24.035277+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.986",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RDH12 were set to ",
"entity_name": "RDH12",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:41:58.685442+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.985",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RBBP8 as ready",
"entity_name": "RBBP8",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:41:58.678201+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.985",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rbbp8 has been classified as Green List (High Evidence).",
"entity_name": "RBBP8",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:41:55.584992+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.985",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RBBP8 were changed from Seckel syndrome 2, 606744 (3) to Jawad syndrome MIM#251255; Seckel syndrome 2 MIM#606744",
"entity_name": "RBBP8",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:41:43.535729+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.984",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RBBP8 were set to ",
"entity_name": "RBBP8",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:41:19.793579+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.983",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAX as ready",
"entity_name": "RAX",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:41:19.750707+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.983",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rax has been classified as Green List (High Evidence).",
"entity_name": "RAX",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:41:16.396433+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.983",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAX were changed from Microphthalmia, isolated 3, 611038 (3) to Microphthalmia, syndromic 16, MIM #611038",
"entity_name": "RAX",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:41:04.574822+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.982",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAX were set to ",
"entity_name": "RAX",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:40:41.439973+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.981",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RARS2 as ready",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:40:41.433180+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.981",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rars2 has been classified as Green List (High Evidence).",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:40:37.642493+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.981",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RARS2 were changed from Pontocerebellar hypoplasia, type 6, 611523 (3) to Pontocerebellar hypoplasia, type 6, MIM#611523",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:40:26.663334+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.980",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RARS2 were set to ",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:40:03.632131+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAPSN as ready",
"entity_name": "RAPSN",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:40:03.621571+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rapsn has been classified as Green List (High Evidence).",
"entity_name": "RAPSN",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:39:59.514602+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAPSN were changed from Fetal akinesia deformation sequence, 208150 (3) to Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency MIM#616326; Fetal akinesia deformation sequence 2 MIM#618388",
"entity_name": "RAPSN",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:39:48.485848+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.978",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAPSN were set to ",
"entity_name": "RAPSN",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:39:23.560695+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAG2 as ready",
"entity_name": "RAG2",
"entity_type": "gene"
}
]
}