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{
"count": 220377,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=48",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=46",
"results": [
{
"created": "2026-01-29T14:32:48.153006+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.30",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: KCNQ1 was added\ngene: KCNQ1 was added to Adrenal insufficiency. Sources: Expert Review Amber,Genomics England PanelApp\nMode of inheritance for gene: KCNQ1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: KCNQ1 were set to 29097701\nPhenotypes for gene: KCNQ1 were set to Hypopituitarism, MONDO:0005152; Long QT syndrome 1 (192500)",
"entity_name": "KCNQ1",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:32:16.331078+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.29",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene ESRP2 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:32:16.276795+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.29",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: ESRP2 was added\ngene: ESRP2 was added to Adrenal insufficiency. Sources: Expert Review Amber,Expert list\nMode of inheritance for gene: ESRP2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: ESRP2 were set to 29805042\nPhenotypes for gene: ESRP2 were set to Cleft palate, MONDO:0016064; Hypopituitarism MONDO:0005152",
"entity_name": "ESRP2",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:31:42.726807+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.28",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CDON from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:31:42.652332+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.28",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CDON was added\ngene: CDON was added to Adrenal insufficiency. Sources: Expert Review Amber,Genomics England PanelApp\nMode of inheritance for gene: CDON was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: CDON were set to 21802063; 29749693; 32729136; 33270637; 26529631; 27974186\nPhenotypes for gene: CDON were set to Holoprosencephaly 11 (614226)",
"entity_name": "CDON",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:30:52.073945+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.27",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene ARNT2 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:30:52.002552+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.27",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: ARNT2 was added\ngene: ARNT2 was added to Adrenal insufficiency. Sources: Expert Review Amber,Literature,Genomics England PanelApp,Genetic Health Queensland\nMode of inheritance for gene: ARNT2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ARNT2 were set to 24022475, 11381139\nPhenotypes for gene: ARNT2 were set to Webb-Dattani syndrome 615926",
"entity_name": "ARNT2",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:28:36.774159+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.26",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene ZRSR2 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:28:36.703039+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.26",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: ZRSR2 was added\ngene: ZRSR2 was added to Adrenal insufficiency. Sources: Expert Review Green,Literature\nMode of inheritance for gene: ZRSR2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: ZRSR2 were set to 38158857\nPhenotypes for gene: ZRSR2 were set to Orofaciodigital syndrome XXI, MIM# 301132",
"entity_name": "ZRSR2",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:27:51.743838+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.25",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene TBX19 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:27:51.692336+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.25",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: TBX19 was added\ngene: TBX19 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX19 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TBX19 were set to 15613420, 31998673, 11290323, 15476446, 22170728\nPhenotypes for gene: TBX19 were set to Adrenocorticotropic hormone deficiency, 201400",
"entity_name": "TBX19",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:27:11.570444+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.24",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene TBC1D32 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:27:11.503681+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.24",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: TBC1D32 was added\ngene: TBC1D32 was added to Adrenal insufficiency. Sources: Expert Review Green,Literature\nMode of inheritance for gene: TBC1D32 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TBC1D32 were set to 32573025; 32060556; 24285566; 31130284; 36826837; 40319332\nPhenotypes for gene: TBC1D32 were set to Syndromic hypopituitarism",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:26:46.317284+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.23",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene SOX3 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:26:46.258365+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.23",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SOX3 was added\ngene: SOX3 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\nSV/CNV tags were added to gene: SOX3.\nMode of inheritance for gene: SOX3 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: SOX3 were set to 24346842; 15800844; 21289259; 24737742\nPhenotypes for gene: SOX3 were set to Panhypopituitarism, X-linked (312000); Mental retardation, X-linked, with isolated growth hormone deficiency (300123)",
"entity_name": "SOX3",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:24:12.557438+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.22",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene ROBO1 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:24:12.498803+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.22",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: ROBO1 was added\ngene: ROBO1 was added to Adrenal insufficiency. Sources: Expert Review Green,Literature\nMode of inheritance for gene: ROBO1 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal\nPublications for gene: ROBO1 were set to PMID: 30530901; 30692597; 33270637; 28402530\nPhenotypes for gene: ROBO1 were set to Pituitary hormone deficiency, combined or isolated, 8, MIM#\t620303",
"entity_name": "ROBO1",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:22:24.161239+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.21",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene HESX1 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:22:24.046610+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.21",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: HESX1 was added\ngene: HESX1 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: HESX1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: HESX1 were set to 14561704; 26781211; 11136712; 16940453\nPhenotypes for gene: HESX1 were set to Growth hormone deficiency with pituitary anomalies (182230); Pituitary hormone deficiency, combined, 5 (182230)",
"entity_name": "HESX1",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:20:19.580520+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.20",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene OTX2 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:20:19.529354+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.20",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: OTX2 was added\ngene: OTX2 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: OTX2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: OTX2 were set to 19965921; 22715480; 18628516; 18728160\nPhenotypes for gene: OTX2 were set to Pituitary hormone deficiency, combined, 6 (613986); Microphthalmia, syndromic 5 (610125)",
"entity_name": "OTX2",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:19:46.618873+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.19",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene LHX4 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:19:46.569066+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.19",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: LHX4 was added\ngene: LHX4 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\ntreatable tags were added to gene: LHX4.\nMode of inheritance for gene: LHX4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: LHX4 were set to 18073311; 18445675; 11567216\nPhenotypes for gene: LHX4 were set to Pituitary hormone deficiency, combined, 4 (262700)",
"entity_name": "LHX4",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:19:40.164321+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.18",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene LHX3 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:19:40.105209+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: LHX3 was added\ngene: LHX3 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\ntreatable tags were added to gene: LHX3.\nMode of inheritance for gene: LHX3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LHX3 were set to Pituitary hormone deficiency, combined, 3 (221750)",
"entity_name": "LHX3",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:19:21.832568+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.17",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene HID1 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:19:21.778710+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.17",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: HID1 was added\ngene: HID1 was added to Adrenal insufficiency. Sources: Expert Review Green,Literature\nMode of inheritance for gene: HID1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HID1 were set to 33999436\nPhenotypes for gene: HID1 were set to Developmental and epileptic encephalopathy 105 with hypopituitarism MIM#619983",
"entity_name": "HID1",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:17:01.453844+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.16",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene GLI3 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:17:01.388270+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.16",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: GLI3 was added\ngene: GLI3 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp,Genomics England PanelApp\nMode of inheritance for gene: GLI3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: GLI3 were set to 24736735; 15739154; 9054938 10945658 11693785\nPhenotypes for gene: GLI3 were set to Greig cephalopolysyndactyly syndrome (175700); Pallister-Hall syndrome (146510)",
"entity_name": "GLI3",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:16:11.947099+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.15",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene GLI2 from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:16:11.892489+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.15",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: GLI2 was added\ngene: GLI2 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp,Victorian Clinical Genetics Services\nMode of inheritance for gene: GLI2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: GLI2 were set to 14581620; 17096318; 33235745; 27585885; 15994174; 20685856; 30629636; 30583238\nPhenotypes for gene: GLI2 were set to Culler-Jones syndrome (615849); Holoprosencephaly 9 (610829)",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:12:03.428421+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.172",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Phenotypes for gene: FGF17 were changed from to Hypogonadotropic hypogonadism 20 with or without anosmia, MIM# 615270",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:09:32.393669+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.14",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene NR0B1 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:09:32.333145+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.14",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: NR0B1 was added\ngene: NR0B1 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services\nSV/CNV tags were added to gene: NR0B1.\nMode of inheritance for gene: NR0B1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: NR0B1 were set to 19508677; 26030781\nPhenotypes for gene: NR0B1 were set to Adrenal hypoplasia, congenital (MIM# 300200); 46XY sex reversal 2, dosage-sensitive, MIM#\t300018",
"entity_name": "NR0B1",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:03:02.031700+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.13",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CYP11B2 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:03:01.944243+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.13",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CYP11B2 was added\ngene: CYP11B2 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services\ntreatable tags were added to gene: CYP11B2.\nMode of inheritance for gene: CYP11B2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP11B2 were set to 8439335; 9360501; 15240589; 9814506; 12788848; 8772616\nPhenotypes for gene: CYP11B2 were set to Hypoaldosteronism, congenital, due to CMO I deficiency (MIM#203400) or due to CMO II deficiency (MIM#610600).",
"entity_name": "CYP11B2",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:01:15.622762+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.12",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene STAR from panel Congenital adrenal hyperplasia",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:01:15.568489+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.12",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: STAR was added\ngene: STAR was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\nMode of inheritance for gene: STAR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STAR were set to 7892608; 8634702\nPhenotypes for gene: STAR were set to Lipoid adrenal hyperplasia (MIM#201710)",
"entity_name": "STAR",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:01:11.068122+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.11",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene POR from panel Congenital adrenal hyperplasia",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:01:11.014060+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.11",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: POR was added\ngene: POR was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\nMode of inheritance for gene: POR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: POR were set to 27068427\nPhenotypes for gene: POR were set to Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, MIM#201750; Disordered steroidogenesis due to cytochrome P450 oxidoreductase, MIM#613571",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:01:04.122197+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.10",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene HSD3B2 from panel Congenital adrenal hyperplasia",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:01:04.067309+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.10",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: HSD3B2 was added\ngene: HSD3B2 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\nMode of inheritance for gene: HSD3B2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HSD3B2 were set to 1363812; 18252794\nPhenotypes for gene: HSD3B2 were set to Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency, MIM# 201810",
"entity_name": "HSD3B2",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:01:00.257197+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CYP21A2 from panel Congenital adrenal hyperplasia",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:01:00.192089+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CYP21A2 was added\ngene: CYP21A2 was added to Adrenal insufficiency. Sources: Expert Review Green,Expert list,Expert list\nMode of inheritance for gene: CYP21A2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CYP21A2 were set to Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, 201910; Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency, 201910",
"entity_name": "CYP21A2",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:00:55.510625+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.8",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CYP17A1 from panel Congenital adrenal hyperplasia",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:00:55.456531+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.8",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CYP17A1 was added\ngene: CYP17A1 was added to Adrenal insufficiency. Sources: Expert Review Green,Expert list,Expert list\nMode of inheritance for gene: CYP17A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP17A1 were set to PMID: 2843762, 14671162, 2026124\nPhenotypes for gene: CYP17A1 were set to 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2026-01-29T14:00:06.373843+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CYP11B1 from panel Congenital adrenal hyperplasia",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T14:00:06.182729+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CYP11B1 was added\ngene: CYP11B1 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\ntreatable tags were added to gene: CYP11B1.\nMode of inheritance for gene: CYP11B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP11B1 were set to 8768848\nPhenotypes for gene: CYP11B1 were set to Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:56:32.553649+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.6",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CYP11A1 from panel Differences of Sex Development",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:56:32.501860+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.6",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CYP11A1 was added\ngene: CYP11A1 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CYP11A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP11A1 were set to 12161514; 16705068; 18182448; 28425981\nPhenotypes for gene: CYP11A1 were set to Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743",
"entity_name": "CYP11A1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:56:07.417180+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CDKN1C from panel Differences of Sex Development",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:56:07.364749+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CDKN1C was added\ngene: CDKN1C was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CDKN1C was set to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)\nPublications for gene: CDKN1C were set to 22634751; 33076988; 31976094; 31497289\nPhenotypes for gene: CDKN1C were set to IMAGe syndrome, MIM# 614732\nMode of pathogenicity for gene: CDKN1C was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
"entity_name": "CDKN1C",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:53:50.605237+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Genetic Health Queensland; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:53:38.917657+11:00",
"panel_name": "Adrenal insufficiency",
"panel_id": 4523,
"panel_version": "0.3",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "HPO terms changed from to Adrenal insufficiency, HP:0000846; Congenital adrenal hypoplasia, HP:0008244",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:38:25.722886+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.8",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Panel status changed from internal to public",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:38:02.357025+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: STAR as ready",
"entity_name": "STAR",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:38:02.346186+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: star has been classified as Green List (High Evidence).",
"entity_name": "STAR",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:37:57.322054+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: POR as ready",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:37:57.312137+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: por has been classified as Green List (High Evidence).",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:37:50.862715+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: HSD3B2 as ready",
"entity_name": "HSD3B2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:37:50.851689+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: hsd3b2 has been classified as Green List (High Evidence).",
"entity_name": "HSD3B2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:37:40.461243+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CYP21A2 as ready",
"entity_name": "CYP21A2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:37:40.451403+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: cyp21a2 has been classified as Green List (High Evidence).",
"entity_name": "CYP21A2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:37:28.019100+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CYP11B1 as ready",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:37:28.011983+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: cyp11b1 has been classified as Green List (High Evidence).",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:36:31.497141+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene STAR from panel Differences of Sex Development",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:36:31.444954+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: STAR was added\ngene: STAR was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: STAR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STAR were set to 7892608; 8634702\nPhenotypes for gene: STAR were set to Lipoid adrenal hyperplasia (MIM#201710)",
"entity_name": "STAR",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:36:28.535918+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.6",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene POR from panel Differences of Sex Development",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:36:28.481869+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.6",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: POR was added\ngene: POR was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: POR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: POR were set to 27068427\nPhenotypes for gene: POR were set to Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, MIM#201750; Disordered steroidogenesis due to cytochrome P450 oxidoreductase, MIM#613571",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:27:09.210315+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CYP11B1 from panel Differences of Sex Development",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:27:09.154615+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CYP11B1 was added\ngene: CYP11B1 was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Victorian Clinical Genetics Services\ntreatable tags were added to gene: CYP11B1.\nMode of inheritance for gene: CYP11B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP11B1 were set to 8768848\nPhenotypes for gene: CYP11B1 were set to Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010",
"entity_name": "CYP11B1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:24:52.008229+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: HSD3B2 as ready",
"entity_name": "HSD3B2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:24:51.996561+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: hsd3b2 has been classified as Green List (High Evidence).",
"entity_name": "HSD3B2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:24:48.071163+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CYP17A1 as ready",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:24:48.061170+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: cyp17a1 has been classified as Green List (High Evidence).",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:23:52.632963+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene HSD3B2 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:23:52.553300+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: HSD3B2 was added\ngene: HSD3B2 was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HSD3B2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HSD3B2 were set to 1363812; 18252794\nPhenotypes for gene: HSD3B2 were set to Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency, MIM# 201810",
"entity_name": "HSD3B2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:22:50.856185+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.3",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CYP17A1 from panel Hypertension and Aldosterone disorders",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:22:50.802923+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.3",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CYP17A1 was added\ngene: CYP17A1 was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: CYP17A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP17A1 were set to PMID: 2843762, 14671162, 2026124\nPhenotypes for gene: CYP17A1 were set to 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110",
"entity_name": "CYP17A1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:20:30.259236+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.2",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CYP21A2 from panel Hypertension and Aldosterone disorders",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:20:30.206423+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.2",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CYP21A2 was added\ngene: CYP21A2 was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: CYP21A2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CYP21A2 were set to Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, 201910; Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency, 201910",
"entity_name": "CYP21A2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:16:34.528976+11:00",
"panel_name": "Congenital adrenal hyperplasia",
"panel_id": 4522,
"panel_version": "0.1",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "HPO terms changed from to Congenital adrenal hyperplasia, HP:0008258\nPanel types changed to Victorian Clinical Genetics Services; Genetic Health Queensland; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:12:40.628930+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.6",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Panel status changed from internal to public",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:12:30.827510+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: GNA11 as ready",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:12:30.817039+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: gna11 has been classified as Green List (High Evidence).",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:12:13.555132+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: AP2S1 as ready",
"entity_name": "AP2S1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:12:13.547831+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: ap2s1 has been classified as Green List (High Evidence).",
"entity_name": "AP2S1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:11:29.688649+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene GNA11 from panel Hypercalcaemia",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:11:29.626408+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.5",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: GNA11 was added\ngene: GNA11 was added to Familial hypocalciuric hypercalcaemia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GNA11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: GNA11 were set to 23802516; 28833550; 27913609\nPhenotypes for gene: GNA11 were set to Hypocalciuric hypercalcaemia, type II, MIM# 145981; MONDO:0007792",
"entity_name": "GNA11",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:10:52.945485+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene AP2S1 from panel Hypercalcaemia",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:10:52.887414+11:00",
"panel_name": "Familial hypocalciuric hypercalcaemia",
"panel_id": 4525,
"panel_version": "0.4",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: AP2S1 was added\ngene: AP2S1 was added to Familial hypocalciuric hypercalcaemia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AP2S1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: AP2S1 were set to 23222959; 33729479; 33168530; 3204769; 31723423; 29479578\nPhenotypes for gene: AP2S1 were set to Hypocalciuric hypercalcaemia, type III, MIM# 600740; MONDO:0010926",
"entity_name": "AP2S1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:09:43.256498+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.10",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Panel status changed from internal to public",
"entity_name": null,
"entity_type": null
},
{
"created": "2026-01-29T13:08:58.984834+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: RET as ready",
"entity_name": "RET",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:08:58.977495+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: ret has been classified as Green List (High Evidence).",
"entity_name": "RET",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:08:51.012599+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: MEN1 as ready",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:08:51.005052+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: men1 has been classified as Green List (High Evidence).",
"entity_name": "MEN1",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:08:47.324403+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: GCM2 as ready",
"entity_name": "GCM2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:08:47.314683+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: gcm2 has been classified as Green List (High Evidence).",
"entity_name": "GCM2",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:08:41.668788+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: CDKN1B as ready",
"entity_name": "CDKN1B",
"entity_type": "gene"
},
{
"created": "2026-01-29T13:08:41.656248+11:00",
"panel_name": "Hyperparathyroidism",
"panel_id": 4526,
"panel_version": "0.9",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: cdkn1b has been classified as Green List (High Evidence).",
"entity_name": "CDKN1B",
"entity_type": "gene"
}
]
}