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{
"count": 220212,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=4",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2",
"results": [
{
"created": "2026-04-01T16:48:47.950665+11:00",
"panel_name": "Monogenic Diabetes",
"panel_id": 3093,
"panel_version": "0.222",
"user_name": "Sangavi Sivagnanasundram",
"item_type": "panel",
"text": "Added reviews for gene APPL1 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-04-01T16:48:04.139088+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4691",
"user_name": "Sangavi Sivagnanasundram",
"item_type": "entity",
"text": "Tag refuted tag was added to gene: APPL1.",
"entity_name": "APPL1",
"entity_type": "gene"
},
{
"created": "2026-04-01T16:47:49.721755+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4691",
"user_name": "Sangavi Sivagnanasundram",
"item_type": "entity",
"text": "reviewed gene: APPL1: Rating: RED; Mode of pathogenicity: None; Publications: https://search.clinicalgenome.org/CCID:004159; Phenotypes: monogenic diabetes MONDO:0015967; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "APPL1",
"entity_type": "gene"
},
{
"created": "2026-04-01T16:45:04.058392+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4691",
"user_name": "Sangavi Sivagnanasundram",
"item_type": "entity",
"text": "Phenotypes for gene: NME8 were changed from Ciliary dyskinesia, primary, 6, MIM# 610852 to Ciliary dyskinesia, primary, 6, MIM# 610852; primary ciliary dyskinesia MONDO:0016575",
"entity_name": "NME8",
"entity_type": "gene"
},
{
"created": "2026-04-01T16:44:50.054267+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4690",
"user_name": "Sangavi Sivagnanasundram",
"item_type": "entity",
"text": "Added comment: Comment on phenotypes: primary ciliary dyskinesia MONDO:0016575",
"entity_name": "NME8",
"entity_type": "gene"
},
{
"created": "2026-04-01T16:44:50.041282+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4690",
"user_name": "Sangavi Sivagnanasundram",
"item_type": "entity",
"text": "Phenotypes for gene: NME8 were changed from Ciliary dyskinesia, primary, 6, MIM# 610852 to Ciliary dyskinesia, primary, 6, MIM# 610852",
"entity_name": "NME8",
"entity_type": "gene"
},
{
"created": "2026-04-01T16:44:23.177833+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4689",
"user_name": "Sangavi Sivagnanasundram",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: NME8.",
"entity_name": "NME8",
"entity_type": "gene"
},
{
"created": "2026-04-01T16:44:11.386486+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4689",
"user_name": "Sangavi Sivagnanasundram",
"item_type": "entity",
"text": "reviewed gene: NME8: Rating: RED; Mode of pathogenicity: None; Publications: https://search.clinicalgenome.org/CCID:005652; Phenotypes: primary ciliary dyskinesia MONDO:0016575; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NME8",
"entity_type": "gene"
},
{
"created": "2026-04-01T15:28:50.156919+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4689",
"user_name": "Sarah Milton",
"item_type": "entity",
"text": "reviewed gene: PIGM: Rating: AMBER; Mode of pathogenicity: None; Publications: 41782195, 39912323, 39425582, 39119839, 31445883; Phenotypes: hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency, MONDO:0012465; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGM",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:32:00.999887+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.64",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "edited their review of gene: SLC6A6: Changed rating: AMBER",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:31:51.058686+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.64",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "changed review comment from: This gene was reviewed as limited by ClinGen in 2023 however PMID: 41343195 had not yet been published at that time\r\n\r\nPMID: 41343195 four families with Leber congenital amaurosis or early-onset retinal dystrophy, all have homozygous variants in SLC6A6- 2 missense, 1 in frame del, 1 nonsense. Thr249Ile, Ala294Thr, Phe404_Glu449del, Trp113Ter. in 1 family the variant segregated with disease as homozygous in 4 affected siblings and heterozygous in unaffected siblings. Some functional evidence available for the 2 missense demonstrating LOF effects. No clear cardiac phenotype was observed in these families. \r\n\r\nPMIDs: 31345061, 31903486 reported Ala78Glu and Gly399Val homozygous; to: This gene was reviewed as limited by ClinGen in 2023 however PMID: 41343195 had not yet been published at that time\r\n\r\nPMID: 41343195 four families with Leber congenital amaurosis or early-onset retinal dystrophy, all have homozygous variants in SLC6A6- 2 missense, 1 in frame del, 1 nonsense. Thr249Ile, Ala294Thr, Phe404_Glu449del, Trp113Ter. in 1 family the variant segregated with disease as homozygous in 4 affected siblings and heterozygous in unaffected siblings. Some functional evidence available for the 2 missense demonstrating LOF effects. No clear cardiac phenotype was observed in these families- still amber for the cardiac association\r\n\r\nPMIDs: 31345061, 31903486 reported Ala78Glu and Gly399Val homozygous",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:31:24.508664+11:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "1.64",
"user_name": "Lucy Spencer",
"item_type": "panel",
"text": "Added reviews for gene SLC6A6 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-04-01T10:30:08.425549+11:00",
"panel_name": "Aminoacidopathy",
"panel_id": 3929,
"panel_version": "1.143",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: SLC6A6 were changed from hypotaurinemic retinal degeneration and cardiomyopathy MONDO:0007777 to Hypotaurinemic retinal degeneration and cardiomyopathy MMI#145350",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:29:58.994931+11:00",
"panel_name": "Aminoacidopathy",
"panel_id": 3929,
"panel_version": "1.142",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Publications for gene: SLC6A6 were set to 31903486; 31345061",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:29:50.612634+11:00",
"panel_name": "Aminoacidopathy",
"panel_id": 3929,
"panel_version": "1.141",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Classified gene: SLC6A6 as Green List (high evidence)",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:29:50.602755+11:00",
"panel_name": "Aminoacidopathy",
"panel_id": 3929,
"panel_version": "1.141",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Gene: slc6a6 has been classified as Green List (High Evidence).",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:29:43.969468+11:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.67",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Publications for gene: SLC6A6 were set to 31345061; 31903486; 29886034",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:29:30.179672+11:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.66",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: SLC6A6 were changed from Hypotaurinaemic retinal degeneration and cardiomyopathy (HTRDC), MIM#145350; Cone-rod retinopathy; cardiomyopathy to Hypotaurinemic retinal degeneration and cardiomyopathy MMI#145350",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:29:19.565023+11:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.65",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Classified gene: SLC6A6 as Green List (high evidence)",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:29:19.555413+11:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.65",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Gene: slc6a6 has been classified as Green List (High Evidence).",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:29:10.222411+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4689",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: SLC6A6 were changed from Hypotaurinaemic retinal degeneration and cardiomyopathy (HTRDC), MIM#145350; Early retinal degeneration; cardiomyopathy to Hypotaurinaemic retinal degeneration and cardiomyopathy MIM#145350",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:28:50.072712+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4688",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Publications for gene: SLC6A6 were set to 31345061; 31903486; 29886034",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:28:38.056281+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4687",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Classified gene: SLC6A6 as Green List (high evidence)",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:28:38.046359+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4687",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Gene: slc6a6 has been classified as Green List (High Evidence).",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:28:23.131455+11:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.64",
"user_name": "Lucy Spencer",
"item_type": "panel",
"text": "Added reviews for gene SLC6A6 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-04-01T10:28:18.182458+11:00",
"panel_name": "Aminoacidopathy",
"panel_id": 3929,
"panel_version": "1.140",
"user_name": "Lucy Spencer",
"item_type": "panel",
"text": "Added reviews for gene SLC6A6 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-04-01T10:27:20.477192+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4686",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: SLC6A6: Rating: GREEN; Mode of pathogenicity: None; Publications: 41343195; Phenotypes: Hypotaurinemic retinal degeneration and cardiomyopathy MMI#145350; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC6A6",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:19:36.088215+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.740",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Publications for gene: SLC6A17 were set to 25704603; 23672601",
"entity_name": "SLC6A17",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:19:03.599690+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.739",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Classified gene: SLC6A17 as Green List (high evidence)",
"entity_name": "SLC6A17",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:19:03.592269+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.739",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Gene: slc6a17 has been classified as Green List (High Evidence).",
"entity_name": "SLC6A17",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:17:54.562043+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.738",
"user_name": "Lucy Spencer",
"item_type": "panel",
"text": "Added reviews for gene SLC6A17 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-04-01T10:17:12.125715+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.102",
"user_name": "Lucy Spencer",
"item_type": "panel",
"text": "Copied gene SLC6A17 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-04-01T10:17:12.063231+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.102",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "gene: SLC6A17 was added\ngene: SLC6A17 was added to Growth failure. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC6A17 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC6A17 were set to 25704603; 23672601; 40897375\nPhenotypes for gene: SLC6A17 were set to Intellectual developmental disorder, autosomal recessive 48, MIM# 616269",
"entity_name": "SLC6A17",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:15:25.546460+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4686",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Publications for gene: SLC6A17 were set to 25704603; 23672601",
"entity_name": "SLC6A17",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:14:56.223640+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4685",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Classified gene: SLC6A17 as Green List (high evidence)",
"entity_name": "SLC6A17",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:14:56.216470+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4685",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Gene: slc6a17 has been classified as Green List (High Evidence).",
"entity_name": "SLC6A17",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:14:34.469976+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4684",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: SLC6A17: Rating: GREEN; Mode of pathogenicity: None; Publications: 25704603, 40897375; Phenotypes: Intellectual developmental disorder, autosomal recessive 48 MIM#616269; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC6A17",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:06:47.857492+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN54 were changed from pontocerebellar hypoplasia type 2A MONDO:0010190 to Pontocerebellar hypoplasia type 2A 277470; Pontocerebellar hypoplasia type 4 225753",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:06:21.679784+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSEN54 were set to 20301773",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:05:54.282387+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:05:13.772683+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.735",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added reviews for gene TSEN54 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-04-01T10:04:12.224939+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN54 were changed from Pontocerebellar hypoplasia type 2A 277470; Pontocerebellar hypoplasia type 4 225753; Ataxia to Pontocerebellar hypoplasia type 2A 277470; Pontocerebellar hypoplasia type 4 225753",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:03:44.260637+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSEN54 were set to 24938831",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2026-04-01T10:03:17.126338+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.4682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TSEN54: Added comment: Reports from PMID 32697043, PMID 35962274, PMID 41825724, PMID 32214227, PMID 39400946, PMID 39634246, PMID 38347586, PMID 39034883, PMID 29410950, PMID 27570394, and PMID 34085948 add a total of 30 patients from 28 unrelated families with autosomal recessive TSEN54 variants (predominantly the founder missense c.919G>T) causing pontocerebellar hypoplasia with microcephaly, severe developmental delay, seizures and characteristic cerebellar‑pontine hypoplasia. PMID 39034883 provides functional validation using patient‑derived iPSC organoids that recapitulate the neuroanatomical phenotype.\r\n\r\nMOI changed to biallelic as evidence for mono allelic association is very limited.; Changed publications: 41825724, 39634246, 39400946, 39034883, 38622473, 38347586, 35962274, 34085948, 32697043, 32214227, 29410950, 27570394, 27430971; Changed phenotypes: Pontocerebellar hypoplasia type 2A 277470, Pontocerebellar hypoplasia type 4 225753",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:07:04.587592+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TY as ready",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:07:04.575598+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-ty has been classified as Green List (High Evidence).",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:52.677451+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TY as ready",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:52.662974+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-ty has been classified as Green List (High Evidence).",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:41.238504+11:00",
"panel_name": "Hereditary Neuropathy",
"panel_id": 3070,
"panel_version": "1.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TY as ready",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:41.230950+11:00",
"panel_name": "Hereditary Neuropathy",
"panel_id": 3070,
"panel_version": "1.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-ty has been classified as Green List (High Evidence).",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:29.399647+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TY as ready",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:29.386661+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-ty has been classified as Green List (High Evidence).",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:19.035763+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.356",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TY as ready",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:19.025273+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.356",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-ty has been classified as Green List (High Evidence).",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:05.608553+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TY as ready",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:06:05.598045+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-ty has been classified as Green List (High Evidence).",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:05:53.709706+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "1.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag somatic was removed from gene: MT-TY.",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:05:31.553883+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.256",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TY from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T19:05:31.472401+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TY was added\ngene: MT-TY was added to Syndromic Retinopathy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TY.\nMode of inheritance for gene gene: MT-TY was set to MITOCHONDRIAL\nPublications for gene: MT-TY were set to 11071502; 11756614; 11594340; 33279411; 30643656; 32684384; 32485333; 33279411\nPhenotypes for gene: MT-TY were set to Mitochondrial disease (MONDO:0044970), MT-TY-related",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:05:29.017257+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.46",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TY from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T19:05:28.856455+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TY was added\ngene: MT-TY was added to Rhabdomyolysis and Metabolic Myopathy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TY.\nMode of inheritance for gene gene: MT-TY was set to MITOCHONDRIAL\nPublications for gene: MT-TY were set to 11071502; 11756614; 11594340; 33279411; 30643656; 32684384; 32485333; 33279411\nPhenotypes for gene: MT-TY were set to Mitochondrial disease (MONDO:0044970), MT-TY-related",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:05:14.096670+11:00",
"panel_name": "Hereditary Neuropathy",
"panel_id": 3070,
"panel_version": "1.190",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TY from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T19:05:13.928201+11:00",
"panel_name": "Hereditary Neuropathy",
"panel_id": 3070,
"panel_version": "1.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TY was added\ngene: MT-TY was added to Hereditary Neuropathy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TY.\nMode of inheritance for gene gene: MT-TY was set to MITOCHONDRIAL\nPublications for gene: MT-TY were set to 11071502; 11756614; 11594340; 33279411; 30643656; 32684384; 32485333; 33279411\nPhenotypes for gene: MT-TY were set to Mitochondrial disease (MONDO:0044970), MT-TY-related",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:04:58.188002+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.405",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TY from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T19:04:57.891995+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TY was added\ngene: MT-TY was added to Genetic Epilepsy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TY.\nMode of inheritance for gene gene: MT-TY was set to MITOCHONDRIAL\nPublications for gene: MT-TY were set to 11071502; 11756614; 11594340; 33279411; 30643656; 32684384; 32485333; 33279411\nPhenotypes for gene: MT-TY were set to Mitochondrial disease (MONDO:0044970), MT-TY-related",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:04:06.926998+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.356",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TY from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T19:04:06.724833+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.356",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TY was added\ngene: MT-TY was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TY.\nMode of inheritance for gene gene: MT-TY was set to MITOCHONDRIAL\nPublications for gene: MT-TY were set to 11071502; 11756614; 11594340; 33279411; 30643656; 32684384; 32485333; 33279411\nPhenotypes for gene: MT-TY were set to Mitochondrial disease (MONDO:0044970), MT-TY-related",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:03:28.375383+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.201",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TY from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T19:03:28.143833+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TY was added\ngene: MT-TY was added to Ataxia. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TY.\nMode of inheritance for gene gene: MT-TY was set to MITOCHONDRIAL\nPublications for gene: MT-TY were set to 11071502; 11756614; 11594340; 33279411; 30643656; 32684384; 32485333; 33279411\nPhenotypes for gene: MT-TY were set to Mitochondrial disease (MONDO:0044970), MT-TY-related",
"entity_name": "MT-TY",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:49.389094+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:49.378965+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:39.296143+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:39.283481+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:25.686620+11:00",
"panel_name": "Monogenic Diabetes",
"panel_id": 3093,
"panel_version": "0.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:25.679048+11:00",
"panel_name": "Monogenic Diabetes",
"panel_id": 3093,
"panel_version": "0.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:12.755959+11:00",
"panel_name": "Hereditary Neuropathy",
"panel_id": 3070,
"panel_version": "1.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:12.748926+11:00",
"panel_name": "Hereditary Neuropathy",
"panel_id": 3070,
"panel_version": "1.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:00.506022+11:00",
"panel_name": "Dystonia and Chorea",
"panel_id": 290,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:01:00.496137+11:00",
"panel_name": "Dystonia and Chorea",
"panel_id": 290,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:00:47.881590+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:00:47.871555+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:00:36.543131+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:00:36.535908+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:00:24.536900+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:00:24.529600+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:00:10.829071+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.610",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T19:00:10.819534+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.610",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:59:58.474732+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.404",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:59:58.467516+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.404",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:59:46.843437+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:59:46.836149+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:59:35.676161+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TW as ready",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:59:35.665783+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tw has been classified as Green List (High Evidence).",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:58:39.346134+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.255",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TW from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T18:58:39.251580+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TW was added\ngene: MT-TW was added to Syndromic Retinopathy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TW.\nMode of inheritance for gene gene: MT-TW was set to MITOCHONDRIAL\nPublications for gene: MT-TW were set to 7695240; 9266739; 9673981; 12776230; 15054399; 18337306; 19809478; 26524491; 23841600; 30937556\nPhenotypes for gene: MT-TW were set to Mitochondrial disease (MONDO:0044970), MT-TW-related",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:58:37.739144+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.610",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TW from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T18:58:37.572090+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.610",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TW was added\ngene: MT-TW was added to Regression. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TW.\nMode of inheritance for gene gene: MT-TW was set to MITOCHONDRIAL\nPublications for gene: MT-TW were set to 7695240; 9266739; 9673981; 12776230; 15054399; 18337306; 19809478; 26524491; 23841600; 30937556\nPhenotypes for gene: MT-TW were set to Mitochondrial disease (MONDO:0044970), MT-TW-related",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:57:58.010445+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.72",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TW from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-03-31T18:57:57.835151+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TW was added\ngene: MT-TW was added to Optic Atrophy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TW.\nMode of inheritance for gene gene: MT-TW was set to MITOCHONDRIAL\nPublications for gene: MT-TW were set to 7695240; 9266739; 9673981; 12776230; 15054399; 18337306; 19809478; 26524491; 23841600; 30937556\nPhenotypes for gene: MT-TW were set to Mitochondrial disease (MONDO:0044970), MT-TW-related",
"entity_name": "MT-TW",
"entity_type": "gene"
},
{
"created": "2026-03-31T18:57:17.711437+11:00",
"panel_name": "Monogenic Diabetes",
"panel_id": 3093,
"panel_version": "0.221",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TW from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
}
]
}