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{
"count": 220488,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=82",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=80",
"results": [
{
"created": "2025-12-18T15:23:28.978640+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3811",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: JAG1 were changed from Alagille syndrome 1, MIM# 118450; Charcot-Marie-Tooth disease, axonal, type 2HH, MIM# 619574 to Alagille syndrome due to a JAG1 point mutation MONDO:0016862; Charcot-Marie-Tooth disease, axonal, type 2HH MIM#619574",
"entity_name": "JAG1",
"entity_type": "gene"
},
{
"created": "2025-12-18T15:23:06.629074+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3810",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: JAG1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Alagille syndrome due to a JAG1 point mutation MONDO:0016862, Charcot-Marie-Tooth disease, axonal, type 2HH MIM#619574; Mode of inheritance: None",
"entity_name": "JAG1",
"entity_type": "gene"
},
{
"created": "2025-12-18T15:20:37.213425+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3810",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: ITSN2 were changed from Nephrotic syndrome to Nephrotic syndrome MONDO:0005377, ITSN2-related",
"entity_name": "ITSN2",
"entity_type": "gene"
},
{
"created": "2025-12-18T15:10:39.328144+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3809",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Publications for gene: ITGB4 were set to 11328943; 9670011; 33225458; 30079450; 29380424; 29198538; 28557647",
"entity_name": "ITGB4",
"entity_type": "gene"
},
{
"created": "2025-12-18T15:10:06.842487+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3808",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "changed review comment from: Updating OMIMs, 2 listed below are now attached to different genes. Both current OMIMs are recessive only; to: Updating OMIMs, 2 listed below are now attached to different genes. Both current OMIMs are recessive only\r\n\r\nDominant reports appear to be rare, PMID: 35822394, 26817667, 36813478",
"entity_name": "ITGB4",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:56:17.720164+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3808",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: ITGB4 were changed from Epidermolysis bullosa of hands and feet, MIM# 131800; Epidermolysis bullosa, junctional, non-Herlitz type, MIM# 226650; Epidermolysis bullosa, junctional, with pyloric atresia, MIM# 226730 to Epidermolysis bullosa, junctional 5A, intermediate MIM#619816; Epidermolysis bullosa, junctional 5B, with pyloric atresia MIM#226730",
"entity_name": "ITGB4",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:55:57.940808+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3807",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: ITGB4: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Epidermolysis bullosa, junctional 5A, intermediate MIM#619816, Epidermolysis bullosa, junctional 5B, with pyloric atresia MIM#226730; Mode of inheritance: None",
"entity_name": "ITGB4",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:38:41.627846+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3807",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: ITFG2 were changed from Neurodevelopmental abnormality; Intellectual disability; Developmental regression; Ataxia to Neurodevelopmental disorder (MONDO:0700092), ITFG2-related",
"entity_name": "ITFG2",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:36:34.347518+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3806",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: ISPD were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, MIM# 614643; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, MIM# 616052 to Myopathy caused by variation in CRPPA MONDO:0100530; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, MIM# 614643; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, MIM# 616052",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:36:09.653678+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3805",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: ISPD: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Myopathy caused by variation in CRPPA MONDO:0100530; Mode of inheritance: None",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:33:18.496835+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3805",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "Phenotypes for gene: ISLR2 were changed from hydrocephalus; arthrogryposis; abdominal distension to Multiple congenital anomalies MONDO:0019042, ISLR2-related",
"entity_name": "ISLR2",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:59.809980+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TF as ready",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:59.799818+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tf has been classified as Green List (High Evidence).",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:46.834211+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TF as ready",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:46.814159+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tf has been classified as Green List (High Evidence).",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:32.567059+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "1.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TF as ready",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:32.557337+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "1.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tf has been classified as Green List (High Evidence).",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:20.948411+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TF as ready",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:20.941627+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tf has been classified as Green List (High Evidence).",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:08.758636+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.308",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TF as ready",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:12:08.751851+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.308",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tf has been classified as Green List (High Evidence).",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:11:50.638177+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TF as ready",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:11:50.627869+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tf has been classified as Green List (High Evidence).",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:11:24.696119+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.41",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TF from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T14:11:24.609482+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TF was added\ngene: MT-TF was added to Stroke. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TF.\nMode of inheritance for gene gene: MT-TF was set to MITOCHONDRIAL\nPublications for gene: MT-TF were set to 14659412; 9771776; 16806928; 21060018; 31463198; 32419253; 34607911; 21424749; 15184630; 20142618; 28267784; 31722346; 35472031; 9636664; 21882289; 16769874; 21914246; 31009750; 18977334\nPhenotypes for gene: MT-TF were set to Mitochondrial disease (MONDO:0044970), MT-TF-related",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:11:24.422238+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.37",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TF from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T14:11:24.244098+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TF was added\ngene: MT-TF was added to Rhabdomyolysis and Metabolic Myopathy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TF.\nMode of inheritance for gene gene: MT-TF was set to MITOCHONDRIAL\nPublications for gene: MT-TF were set to 14659412; 9771776; 16806928; 21060018; 31463198; 32419253; 34607911; 21424749; 15184630; 20142618; 28267784; 31722346; 35472031; 9636664; 21882289; 16769874; 21914246; 31009750; 18977334\nPhenotypes for gene: MT-TF were set to Mitochondrial disease (MONDO:0044970), MT-TF-related",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:11:08.496248+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TF from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T14:11:08.346922+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TF was added\ngene: MT-TF was added to Retinitis pigmentosa. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TF.\nMode of inheritance for gene gene: MT-TF was set to MITOCHONDRIAL\nPublications for gene: MT-TF were set to 14659412; 9771776; 16806928; 21060018; 31463198; 32419253; 34607911; 21424749; 15184630; 20142618; 28267784; 31722346; 35472031; 9636664; 21882289; 16769874; 21914246; 31009750; 18977334\nPhenotypes for gene: MT-TF were set to Mitochondrial disease (MONDO:0044970), MT-TF-related",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:11:04.659837+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "1.47",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TF from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T14:11:04.448978+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "1.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TF was added\ngene: MT-TF was added to Hereditary Neuropathy - complex. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TF.\nMode of inheritance for gene gene: MT-TF was set to MITOCHONDRIAL\nPublications for gene: MT-TF were set to 14659412; 9771776; 16806928; 21060018; 31463198; 32419253; 34607911; 21424749; 15184630; 20142618; 28267784; 31722346; 35472031; 9636664; 21882289; 16769874; 21914246; 31009750; 18977334\nPhenotypes for gene: MT-TF were set to Mitochondrial disease (MONDO:0044970), MT-TF-related",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:52.573556+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TH as ready",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:52.561657+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-th has been classified as Green List (High Evidence).",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:47.647000+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.314",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TF from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T14:10:47.343417+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TF was added\ngene: MT-TF was added to Genetic Epilepsy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TF.\nMode of inheritance for gene gene: MT-TF was set to MITOCHONDRIAL\nPublications for gene: MT-TF were set to 14659412; 9771776; 16806928; 21060018; 31463198; 32419253; 34607911; 21424749; 15184630; 20142618; 28267784; 31722346; 35472031; 9636664; 21882289; 16769874; 21914246; 31009750; 18977334\nPhenotypes for gene: MT-TF were set to Mitochondrial disease (MONDO:0044970), MT-TF-related",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:40.916376+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TH as ready",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:40.905479+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-th has been classified as Green List (High Evidence).",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:29.027547+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TH as ready",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:29.019768+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-th has been classified as Green List (High Evidence).",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:16.514161+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TH as ready",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:16.502587+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-th has been classified as Green List (High Evidence).",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:02.757109+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TH as ready",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:10:02.749022+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-th has been classified as Green List (High Evidence).",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:09:53.545588+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.308",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TF from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T14:09:53.354015+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.308",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TF was added\ngene: MT-TF was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TF.\nMode of inheritance for gene gene: MT-TF was set to MITOCHONDRIAL\nPublications for gene: MT-TF were set to 14659412; 9771776; 16806928; 21060018; 31463198; 32419253; 34607911; 21424749; 15184630; 20142618; 28267784; 31722346; 35472031; 9636664; 21882289; 16769874; 21914246; 31009750; 18977334\nPhenotypes for gene: MT-TF were set to Mitochondrial disease (MONDO:0044970), MT-TF-related",
"entity_name": "MT-TF",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:09:47.269017+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TH as ready",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:09:47.261271+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-th has been classified as Green List (High Evidence).",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:09:35.284798+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TH as ready",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:09:35.276836+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-th has been classified as Green List (High Evidence).",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:08:18.796430+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:08:18.785870+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:08:05.392101+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:08:05.384857+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:07:53.572227+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "1.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:07:53.562899+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "1.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:07:42.167776+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:07:42.157926+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:07:30.314357+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:07:30.304479+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:07:18.151180+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:07:18.143997+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:06:59.415766+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:06:59.408722+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:06:46.163993+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:06:46.157081+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:06:35.238466+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TG as ready",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T14:06:35.231465+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-tg has been classified as Green List (High Evidence).",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:37:19.368066+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.40",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TH from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:37:19.294096+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TH was added\ngene: MT-TH was added to Stroke. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TH.\nMode of inheritance for gene gene: MT-TH was set to MITOCHONDRIAL\nPublications for gene: MT-TH were set to 12682337; 14967777; 15111688; 21704194; 21931169; 23696415; 35092007; 24920829; 21704194\nPhenotypes for gene: MT-TH were set to Mitochondrial disease (MONDO:0044970), MT-TH-related",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:37:19.100562+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.228",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TH from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:37:18.984710+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TH was added\ngene: MT-TH was added to Retinitis pigmentosa. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TH.\nMode of inheritance for gene gene: MT-TH was set to MITOCHONDRIAL\nPublications for gene: MT-TH were set to 12682337; 14967777; 15111688; 21704194; 21931169; 23696415; 35092007; 24920829; 21704194\nPhenotypes for gene: MT-TH were set to Mitochondrial disease (MONDO:0044970), MT-TH-related",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:37:16.833688+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.67",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TH from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:37:16.664834+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TH was added\ngene: MT-TH was added to Optic Atrophy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TH.\nMode of inheritance for gene gene: MT-TH was set to MITOCHONDRIAL\nPublications for gene: MT-TH were set to 12682337; 14967777; 15111688; 21704194; 21931169; 23696415; 35092007; 24920829; 21704194\nPhenotypes for gene: MT-TH were set to Mitochondrial disease (MONDO:0044970), MT-TH-related",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:36:38.947312+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.313",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TH from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:36:37.764312+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TH was added\ngene: MT-TH was added to Genetic Epilepsy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TH.\nMode of inheritance for gene gene: MT-TH was set to MITOCHONDRIAL\nPublications for gene: MT-TH were set to 12682337; 14967777; 15111688; 21704194; 21931169; 23696415; 35092007; 24920829; 21704194\nPhenotypes for gene: MT-TH were set to Mitochondrial disease (MONDO:0044970), MT-TH-related",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:35:45.231111+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.307",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TH from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:35:44.998425+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TH was added\ngene: MT-TH was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TH.\nMode of inheritance for gene gene: MT-TH was set to MITOCHONDRIAL\nPublications for gene: MT-TH were set to 12682337; 14967777; 15111688; 21704194; 21931169; 23696415; 35092007; 24920829; 21704194\nPhenotypes for gene: MT-TH were set to Mitochondrial disease (MONDO:0044970), MT-TH-related",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:35:07.304230+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TH from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:35:07.144649+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TH was added\ngene: MT-TH was added to Cataract. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TH.\nMode of inheritance for gene gene: MT-TH was set to MITOCHONDRIAL\nPublications for gene: MT-TH were set to 12682337; 14967777; 15111688; 21704194; 21931169; 23696415; 35092007; 24920829; 21704194\nPhenotypes for gene: MT-TH were set to Mitochondrial disease (MONDO:0044970), MT-TH-related",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:34:28.874313+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.164",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TH from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:34:28.712397+11:00",
"panel_name": "Ataxia",
"panel_id": 271,
"panel_version": "1.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TH was added\ngene: MT-TH was added to Ataxia. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TH.\nMode of inheritance for gene gene: MT-TH was set to MITOCHONDRIAL\nPublications for gene: MT-TH were set to 12682337; 14967777; 15111688; 21704194; 21931169; 23696415; 35092007; 24920829; 21704194\nPhenotypes for gene: MT-TH were set to Mitochondrial disease (MONDO:0044970), MT-TH-related",
"entity_name": "MT-TH",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:34:14.194216+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.36",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TG from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:34:13.926329+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TG was added\ngene: MT-TG was added to Rhabdomyolysis and Metabolic Myopathy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TG.\nMode of inheritance for gene gene: MT-TG was set to MITOCHONDRIAL\nPublications for gene: MT-TG were set to 8079988; 9199564; 11971101; 16120360; 32337339; 35432167; 10090480\nPhenotypes for gene: MT-TG were set to Mitochondrial disease (MONDO:0044970), MT-TG-related",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:33:57.588485+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.227",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TG from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:33:57.462240+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TG was added\ngene: MT-TG was added to Retinitis pigmentosa. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TG.\nMode of inheritance for gene gene: MT-TG was set to MITOCHONDRIAL\nPublications for gene: MT-TG were set to 8079988; 9199564; 11971101; 16120360; 32337339; 35432167; 10090480\nPhenotypes for gene: MT-TG were set to Mitochondrial disease (MONDO:0044970), MT-TG-related",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:33:54.898208+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.66",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TG from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:33:54.723613+11:00",
"panel_name": "Optic Atrophy",
"panel_id": 149,
"panel_version": "1.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TG was added\ngene: MT-TG was added to Optic Atrophy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TG.\nMode of inheritance for gene gene: MT-TG was set to MITOCHONDRIAL\nPublications for gene: MT-TG were set to 8079988; 9199564; 11971101; 16120360; 32337339; 35432167; 10090480\nPhenotypes for gene: MT-TG were set to Mitochondrial disease (MONDO:0044970), MT-TG-related",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:33:15.129297+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "1.46",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TG from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:33:14.934134+11:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "1.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TG was added\ngene: MT-TG was added to Hereditary Neuropathy - complex. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TG.\nMode of inheritance for gene gene: MT-TG was set to MITOCHONDRIAL\nPublications for gene: MT-TG were set to 8079988; 9199564; 11971101; 16120360; 32337339; 35432167; 10090480\nPhenotypes for gene: MT-TG were set to Mitochondrial disease (MONDO:0044970), MT-TG-related",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:32:56.326691+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.312",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TG from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:32:56.037709+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.312",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TG was added\ngene: MT-TG was added to Genetic Epilepsy. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TG.\nMode of inheritance for gene gene: MT-TG was set to MITOCHONDRIAL\nPublications for gene: MT-TG were set to 8079988; 9199564; 11971101; 16120360; 32337339; 35432167; 10090480\nPhenotypes for gene: MT-TG were set to Mitochondrial disease (MONDO:0044970), MT-TG-related",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:32:04.215694+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.306",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TG from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:32:03.980411+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TG was added\ngene: MT-TG was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TG.\nMode of inheritance for gene gene: MT-TG was set to MITOCHONDRIAL\nPublications for gene: MT-TG were set to 8079988; 9199564; 11971101; 16120360; 32337339; 35432167; 10090480\nPhenotypes for gene: MT-TG were set to Mitochondrial disease (MONDO:0044970), MT-TG-related",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:31:31.465951+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TE as ready",
"entity_name": "MT-TE",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:31:31.451607+11:00",
"panel_name": "Stroke",
"panel_id": 3141,
"panel_version": "1.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-te has been classified as Green List (High Evidence).",
"entity_name": "MT-TE",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:31:24.984283+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.397",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Copied gene MT-TG from panel Mitochondrial disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-18T13:31:24.842522+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MT-TG was added\ngene: MT-TG was added to Cataract. Sources: Expert Review Green,Expert list\nmtDNA tags were added to gene: MT-TG.\nMode of inheritance for gene gene: MT-TG was set to MITOCHONDRIAL\nPublications for gene: MT-TG were set to 8079988; 9199564; 11971101; 16120360; 32337339; 35432167; 10090480\nPhenotypes for gene: MT-TG were set to Mitochondrial disease (MONDO:0044970), MT-TG-related",
"entity_name": "MT-TG",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:31:19.310778+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TE as ready",
"entity_name": "MT-TE",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:31:19.302631+11:00",
"panel_name": "Rhabdomyolysis and Metabolic Myopathy",
"panel_id": 3084,
"panel_version": "1.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mt-te has been classified as Green List (High Evidence).",
"entity_name": "MT-TE",
"entity_type": "gene"
},
{
"created": "2025-12-18T13:31:05.042776+11:00",
"panel_name": "Retinitis pigmentosa",
"panel_id": 277,
"panel_version": "0.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MT-TE as ready",
"entity_name": "MT-TE",
"entity_type": "gene"
}
]
}