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"count": 220497,
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"results": [
{
"created": "2025-12-07T13:03:25.876606+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37393-Gain as ready",
"entity_name": "ISCA-37393-Gain",
"entity_type": "region"
},
{
"created": "2025-12-07T13:03:25.865657+11:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "1.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37393-gain has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37393-Gain",
"entity_type": "region"
},
{
"created": "2025-12-07T13:03:06.837259+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.479",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37393-Gain as ready",
"entity_name": "ISCA-37393-Gain",
"entity_type": "region"
},
{
"created": "2025-12-07T13:03:06.813559+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.479",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37393-gain has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37393-Gain",
"entity_type": "region"
},
{
"created": "2025-12-07T13:02:42.962161+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37393-Gain as ready",
"entity_name": "ISCA-37393-Gain",
"entity_type": "region"
},
{
"created": "2025-12-07T13:02:42.952633+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37393-gain has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37393-Gain",
"entity_type": "region"
},
{
"created": "2025-12-07T13:02:22.290188+11:00",
"panel_name": "Hand and foot malformations",
"panel_id": 3729,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37394-Loss as ready",
"entity_name": "ISCA-37394-Loss",
"entity_type": "region"
},
{
"created": "2025-12-07T13:02:22.266971+11:00",
"panel_name": "Hand and foot malformations",
"panel_id": 3729,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37394-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37394-Loss",
"entity_type": "region"
},
{
"created": "2025-12-07T13:01:54.542991+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37394-Loss as ready",
"entity_name": "ISCA-37394-Loss",
"entity_type": "region"
},
{
"created": "2025-12-07T13:01:54.532624+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37394-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37394-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:56:10.185856+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37396-Loss as ready",
"entity_name": "ISCA-37396-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:56:10.176566+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37396-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37396-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:55:53.354564+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37396-Loss as ready",
"entity_name": "ISCA-37396-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:55:53.347964+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37396-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37396-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:55:38.161710+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37397-Gain as ready",
"entity_name": "ISCA-37397-Gain",
"entity_type": "region"
},
{
"created": "2025-12-06T19:55:38.152493+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37397-gain has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37397-Gain",
"entity_type": "region"
},
{
"created": "2025-12-06T19:55:22.708304+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37397-Loss as ready",
"entity_name": "ISCA-37397-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:55:22.702047+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37397-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37397-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:55:09.473142+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37397-Loss as ready",
"entity_name": "ISCA-37397-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:55:09.464857+11:00",
"panel_name": "Growth failure",
"panel_id": 3631,
"panel_version": "1.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37397-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37397-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:54:53.182148+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37397-Loss as ready",
"entity_name": "ISCA-37397-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:54:53.173356+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37397-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37397-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:54:37.430793+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37400-Gain as ready",
"entity_name": "ISCA-37400-Gain",
"entity_type": "region"
},
{
"created": "2025-12-06T19:54:37.421525+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37400-gain has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37400-Gain",
"entity_type": "region"
},
{
"created": "2025-12-06T19:54:21.333613+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37400-Loss as ready",
"entity_name": "ISCA-37400-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:54:21.327564+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37400-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37400-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:53:58.912110+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37400-Loss as ready",
"entity_name": "ISCA-37400-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:53:58.903384+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37400-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37400-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:53:44.292141+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37400-Loss as ready",
"entity_name": "ISCA-37400-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:53:44.283253+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37400-loss has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37400-Loss",
"entity_type": "region"
},
{
"created": "2025-12-06T19:53:30.515708+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37404-Gain as ready",
"entity_name": "ISCA-37404-Gain",
"entity_type": "region"
},
{
"created": "2025-12-06T19:53:30.506872+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37404-gain has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37404-Gain",
"entity_type": "region"
},
{
"created": "2025-12-06T19:53:09.836977+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked Region: ISCA-37404-Gain as ready",
"entity_name": "ISCA-37404-Gain",
"entity_type": "region"
},
{
"created": "2025-12-06T19:53:09.827702+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Region: isca-37404-gain has been classified as Green List (High Evidence).",
"entity_name": "ISCA-37404-Gain",
"entity_type": "region"
},
{
"created": "2025-12-06T17:21:44.465762+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LRPPRC as ready",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2025-12-06T17:21:44.452226+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lrpprc has been classified as Green List (High Evidence).",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2025-12-06T17:21:40.584594+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LRPPRC were changed from to Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian) MIM#220111",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2025-12-06T17:21:03.263718+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1211",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LRPPRC were set to ",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:43:14.931067+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LRPPRC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LRPPRC",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:42:27.687971+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LIPT2 as ready",
"entity_name": "LIPT2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:42:27.678155+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lipt2 has been classified as Green List (High Evidence).",
"entity_name": "LIPT2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:42:24.852726+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LIPT2 were changed from to Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, MIM# 617668",
"entity_name": "LIPT2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:41:47.603228+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LIPT2 were set to ",
"entity_name": "LIPT2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:41:06.822142+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LIPT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LIPT2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:40:24.833688+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LIAS as ready",
"entity_name": "LIAS",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:40:24.823522+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lias has been classified as Green List (High Evidence).",
"entity_name": "LIAS",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:40:21.618306+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LIAS were changed from to Hyperglycinaemia, lactic acidosis, and seizures, MIM# 614462",
"entity_name": "LIAS",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:39:51.513360+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1205",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LIAS were set to ",
"entity_name": "LIAS",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:38:45.723572+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LIAS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LIAS",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:38:07.660228+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1203",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LARS2 as ready",
"entity_name": "LARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:38:07.650459+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1203",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lars2 has been classified as Green List (High Evidence).",
"entity_name": "LARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:38:04.541240+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1203",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LARS2 were changed from to Perrault syndrome 4; Hydrops, lactic acidosis, and sideroblastic anaemia, MIM# 617021; Leukodystrophy",
"entity_name": "LARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:37:21.755741+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LARS2 were set to ",
"entity_name": "LARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:36:44.693742+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:35:59.973503+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ISCU as ready",
"entity_name": "ISCU",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:35:59.963002+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: iscu has been classified as Green List (High Evidence).",
"entity_name": "ISCU",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:35:57.309292+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ISCU were changed from to Myopathy with lactic acidosis, hereditary, MIM# 255125",
"entity_name": "ISCU",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:35:23.835805+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1199",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ISCU were set to ",
"entity_name": "ISCU",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:34:54.717870+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ISCU was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ISCU",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:34:13.819052+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IARS2 as ready",
"entity_name": "IARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:34:13.809247+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: iars2 has been classified as Green List (High Evidence).",
"entity_name": "IARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:34:08.779790+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IARS2 were changed from to Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia, MIM# 616007",
"entity_name": "IARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:33:40.101453+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IARS2 were set to ",
"entity_name": "IARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:33:09.318031+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IARS2",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:32:26.727948+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSD17B10 as ready",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:32:26.718090+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hsd17b10 has been classified as Green List (High Evidence).",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:32:24.006820+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HSD17B10 were changed from to HSD10 mitochondrial disease, MIM# 300438",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:31:45.635659+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HSD17B10 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "HSD17B10",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:31:02.856932+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSPD1 as ready",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:31:02.849413+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hspd1 has been classified as Green List (High Evidence).",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:31:00.240928+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HSPD1 were changed from to Leukodystrophy, hypomyelinating, 4, MIM# 612233; Spastic paraplegia 13, autosomal dominant, MIM# 605280",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:30:29.439756+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HSPD1 were set to ",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2025-12-06T14:30:00.975942+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HSPD1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "HSPD1",
"entity_type": "gene"
},
{
"created": "2025-12-05T23:17:54.815902+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIBCH as ready",
"entity_name": "HIBCH",
"entity_type": "gene"
},
{
"created": "2025-12-05T23:17:54.808578+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hibch has been classified as Green List (High Evidence).",
"entity_name": "HIBCH",
"entity_type": "gene"
},
{
"created": "2025-12-05T23:17:50.899896+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HIBCH were changed from to 3-hydroxyisobutryl-CoA hydrolase deficiency, MIM# 250620",
"entity_name": "HIBCH",
"entity_type": "gene"
},
{
"created": "2025-12-05T23:14:54.841688+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HIBCH were set to 26026795; 25251209; 24299452; 32677093",
"entity_name": "HIBCH",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:33:49.770981+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HIBCH were set to ",
"entity_name": "HIBCH",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:33:14.929479+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HIBCH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HIBCH",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:32:36.304219+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HCCS as ready",
"entity_name": "HCCS",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:32:36.293289+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hccs has been classified as Green List (High Evidence).",
"entity_name": "HCCS",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:32:33.609264+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HCCS were changed from to Linear skin defects with multiple congenital anomalies 1, MIM# 309801",
"entity_name": "HCCS",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:31:52.742152+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HCCS were set to ",
"entity_name": "HCCS",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:30:43.219671+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HCCS was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "HCCS",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:29:54.354579+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GLRX5 as ready",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:29:54.346988+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: glrx5 has been classified as Green List (High Evidence).",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:29:51.194130+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GLRX5 were changed from to Anaemia, sideroblastic, 3, pyridoxine-refractory, MIM# 616860",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:29:00.973769+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GLRX5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:28:21.359482+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GFM1 as ready",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:28:21.351873+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gfm1 has been classified as Green List (High Evidence).",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:28:09.528996+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GFM1 were changed from to Combined oxidative phosphorylation deficiency 1 MIM#609060",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:27:40.523497+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GFM1 were set to ",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:27:11.753786+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GFM1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:26:22.223511+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FLAD1 as ready",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:26:22.213166+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flad1 has been classified as Green List (High Evidence).",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:26:18.992707+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FLAD1 were changed from to Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency MIM#255100",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:25:35.688767+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FLAD1 were set to ",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:24:55.808132+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FLAD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:24:10.775220+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ETHE1 as ready",
"entity_name": "ETHE1",
"entity_type": "gene"
},
{
"created": "2025-12-05T18:24:10.768008+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.1174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ethe1 has been classified as Green List (High Evidence).",
"entity_name": "ETHE1",
"entity_type": "gene"
}
]
}