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{
"count": 220497,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=94",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=92",
"results": [
{
"created": "2025-12-11T11:39:57.306404+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.148",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: PAX6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:39:49.003134+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.148",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene PAX6 from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:39:04.611920+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.147",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: NODAL: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "NODAL",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:38:49.708142+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.147",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene NODAL from panel Mendeliome",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:37:37.593222+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.146",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: HNRNPU: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HNRNPU",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:37:28.099790+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.146",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene HNRNPU from panel Intellectual disability syndromic and non-syndromic",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:37:21.119828+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.496",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Deleted their review",
"entity_name": "HNRNPU",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:37:18.634830+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.496",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "HNRNPU",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:36:54.867753+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.496",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: HNRNPU: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HNRNPU",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:36:26.378051+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.3766",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene HHIP from panel Pituitary hormone deficiency",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:36:06.497816+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.145",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: HHIP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "HHIP",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:28:10.693578+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.145",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: GPR161 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GPR161",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:27:41.506694+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.144",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Added reviews for gene GPR161 from panel Growth failure",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:27:15.840186+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.143",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GHRH: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "GHRH",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:24:59.109617+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.143",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: FOXH1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FOXH1",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:24:03.630797+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.143",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "commented on gene: BMP2",
"entity_name": "BMP2",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:15:37.300772+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.143",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene HFE2 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:15:37.246949+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.143",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: HFE2 was added\ngene: HFE2 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nnew gene name tags were added to gene: HFE2.\nMode of inheritance for gene: HFE2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HFE2 were set to Hemochromatosis, type 2A, MIM# 602390",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:15:31.795166+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.142",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene HFE from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:15:31.713045+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.142",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: HFE was added\ngene: HFE was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HFE was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HFE were set to Haemochromatosis, MIM# 235200",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:15:25.658940+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.141",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene HAMP from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:15:25.585820+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.141",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: HAMP was added\ngene: HAMP was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HAMP was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HAMP were set to 12469120; 34828384; 15198949\nPhenotypes for gene: HAMP were set to Haemochromatosis, type 2B, MIM# 613313",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:15:16.862157+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.140",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene GNRH1 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:15:16.791981+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.140",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: GNRH1 was added\ngene: GNRH1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GNRH1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GNRH1 were set to 19535795; 19567835; 32134721; 31200363; 26595427\nPhenotypes for gene: GNRH1 were set to Hypogonadotropic hypogonadism 12 with or without anosmia, MIM# 614841",
"entity_name": "GNRH1",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:15:11.388971+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.139",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene FSHB from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:15:11.313576+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.139",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FSHB was added\ngene: FSHB was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: FSHB was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FSHB were set to 8220432; 9280841; 9624193; 9806482; 9271483; 16630814\nPhenotypes for gene: FSHB were set to Hypogonadotropic hypogonadism 24 without anosmia, MIM#229070",
"entity_name": "FSHB",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:15:04.260636+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.138",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene FLRT3 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:15:04.185419+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.138",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FLRT3 was added\ngene: FLRT3 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Red,Expert Review Red,Victorian Clinical Genetics Services\nMode of inheritance for gene: FLRT3 was set to Unknown\nPublications for gene: FLRT3 were set to 23643382; 31200363\nPhenotypes for gene: FLRT3 were set to Hypogonadotropic hypogonadism 21 with anosmia (MIM# 615271)",
"entity_name": "FLRT3",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:14:57.859886+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.137",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene FGF17 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:14:57.788534+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.137",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FGF17 was added\ngene: FGF17 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FGF17 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: FGF17 were set to 23643382; 31748124",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:14:52.395105+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.136",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene FEZF1 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:14:52.355989+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.136",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FEZF1 was added\ngene: FEZF1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Amber\nMode of inheritance for gene: FEZF1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FEZF1 were set to 25192046; 32400067\nPhenotypes for gene: FEZF1 were set to Hypogonadotropic hypogonadism 22, with or without anosmia 616030",
"entity_name": "FEZF1",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:14:44.479254+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.135",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene DUSP6 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:14:44.404396+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.135",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: DUSP6 was added\ngene: DUSP6 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Red\nMode of inheritance for gene: DUSP6 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DUSP6 were set to 23643382; 32389901\nPhenotypes for gene: DUSP6 were set to Hypogonadotropic hypogonadism 19 with or without anosmia - MIM#615269",
"entity_name": "DUSP6",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:14:32.193820+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.134",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene DCAF17 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:14:32.145788+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.134",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: DCAF17 was added\ngene: DCAF17 was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Green,Expert Review Green,Expert Review\nMode of inheritance for gene: DCAF17 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DCAF17 were set to 19026396; 20507343; 35002959; 34877714; 34732557; 34590781\nPhenotypes for gene: DCAF17 were set to Woodhouse-Sakati syndrome, MIM#\t241080",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:14:26.517693+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.133",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CUL4B from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:14:26.465685+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.133",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CUL4B was added\ngene: CUL4B was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert list,Expert Review Green,Expert Review Green,Expert Review Green,Expert Review Green,Expert list,Victorian Clinical Genetics Services\nMode of inheritance for gene: CUL4B was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: CUL4B were set to PMID: 25385192\nPhenotypes for gene: CUL4B were set to Mental retardation, X-linked, syndromic 15 (Cabezas type)\t300354",
"entity_name": "CUL4B",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:14:19.800262+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.132",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CLPP from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:14:19.752418+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.132",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CLPP was added\ngene: CLPP was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Amber,Expert Review Amber,Expert Review\nMode of inheritance for gene: CLPP was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CLPP were set to 23541340; 25956234; 26970254; 27087618; 27650058; 27650058; 27899912\nPhenotypes for gene: CLPP were set to Perrault syndrome 3, MIM# 614129",
"entity_name": "CLPP",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:14:12.997250+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.131",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene CCDC141 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:14:12.765075+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.131",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: CCDC141 was added\ngene: CCDC141 was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Amber,Expert Review Amber,Expert Review\nMode of inheritance for gene: CCDC141 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: CCDC141 were set to 251920460; 28324054; 32520725; 27014940\nPhenotypes for gene: CCDC141 were set to congenital hypogonadotropic hypogonadism, MONDO:0015770, CCDC141-related",
"entity_name": "CCDC141",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:14:06.998661+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.130",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene AXL from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:14:06.952175+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.130",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: AXL was added\ngene: AXL was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Red,Expert Review Red,Expert Review\nMode of inheritance for gene: AXL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: AXL were set to 24476074\nPhenotypes for gene: AXL were set to Hypogonadotropic hypogonadism, MONDO:0018555, AXL-related",
"entity_name": "AXL",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:59.178246+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.129",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene ARHGAP35 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:59.100021+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.129",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: ARHGAP35 was added\ngene: ARHGAP35 was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Expert Review Green,Literature\nMode of inheritance for gene: ARHGAP35 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ARHGAP35 were set to PMID: 36178483\nPhenotypes for gene: ARHGAP35 were set to Hypogonadotropic hypogonadism, MONDO:0015770, ARHGAP35-related",
"entity_name": "ARHGAP35",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:53.007652+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.128",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene ANOS1 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:52.961500+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.128",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: ANOS1 was added\ngene: ANOS1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ANOS1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: ANOS1 were set to 1594017; 8504298; 8989261\nPhenotypes for gene: ANOS1 were set to Hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), MIM# 308700",
"entity_name": "ANOS1",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:44.610879+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.127",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene TFR2 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:44.561625+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.127",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: TFR2 was added\ngene: TFR2 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TFR2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TFR2 were set to 24847265; 29743178\nPhenotypes for gene: TFR2 were set to Haemochromatosis, type 3 (MIM#604250)",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:38.972438+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.126",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene TCF12 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:38.898177+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.126",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: TCF12 was added\ngene: TCF12 was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Expert Review Green,Literature\nMode of inheritance for gene: TCF12 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: TCF12 were set to 32620954\nPhenotypes for gene: TCF12 were set to Hypogonadotropic hypogonadism 26 with or without anosmia, MIM# 619718; Kallmann syndrome",
"entity_name": "TCF12",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:33.576924+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.125",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene TACR3 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:33.510787+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.125",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: TACR3 was added\ngene: TACR3 was added to Pituitary hormone deficiency. Sources: Expert list,Expert Review Green,Expert Review Green,Expert list\nMode of inheritance for gene: TACR3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TACR3 were set to 20332248; 19079066\nPhenotypes for gene: TACR3 were set to Hypogonadotropic hypogonadism 11 with or without anosmia, MIM#\t614840",
"entity_name": "TACR3",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:26.564132+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.124",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene TAC3 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:26.496511+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.124",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: TAC3 was added\ngene: TAC3 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TAC3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TAC3 were set to 19079066; 20332248; 23329188; 22031817\nPhenotypes for gene: TAC3 were set to Hypogonadotropic hypogonadism 10 with or without anosmia (MIM#614839)",
"entity_name": "TAC3",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:20.311987+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.123",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene SPRY4 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:20.267168+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.123",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SPRY4 was added\ngene: SPRY4 was added to Pituitary hormone deficiency. Sources: Expert list,Expert Review Amber,Expert Review Amber,Expert list\ndisputed tags were added to gene: SPRY4.\nMode of inheritance for gene: SPRY4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SPRY4 were set to 23643382\nPhenotypes for gene: SPRY4 were set to Hypogonadotropic hypogonadism 17 with or without anosmia, MIM#\t615266",
"entity_name": "SPRY4",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:15.357427+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.122",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene SOX10 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:15.290060+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.122",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SOX10 was added\ngene: SOX10 was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Green,Expert Review\nMode of inheritance for gene: SOX10 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: SOX10 were set to 23643381; 15004559\nPhenotypes for gene: SOX10 were set to Kallman syndrome; PCWH syndrome (MIM#609136); Waardenburg syndrome, type 2E, with or without neurologic involvement (MIM#611584); Waardenburg syndrome, type 4C (MIM#613266)\nMode of pathogenicity for gene: SOX10 was set to Other",
"entity_name": "SOX10",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:08.983961+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.121",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene SLC40A1 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:08.899577+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.121",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SLC40A1 was added\ngene: SLC40A1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC40A1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SLC40A1 were set to 11431687; 11518736; 15956209; 16351644\nPhenotypes for gene: SLC40A1 were set to Haemochromatosis, type 4, MIM# 606069",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:13:02.930925+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.120",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene SLC29A3 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:13:02.855708+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.120",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SLC29A3 was added\ngene: SLC29A3 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC29A3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC29A3 were set to 18940313; 19336477; 22238637\nPhenotypes for gene: SLC29A3 were set to Histiocytosis-lymphadenopathy plus syndrome, MIM# 602782",
"entity_name": "SLC29A3",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:12:55.895386+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.119",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene SEMA3F from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:55.850762+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.119",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SEMA3F was added\ngene: SEMA3F was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Literature\nMode of inheritance for gene: SEMA3F was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SEMA3F were set to PMID: 33495532\nPhenotypes for gene: SEMA3F were set to Hypogonadotropic hypogonadism",
"entity_name": "SEMA3F",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:12:50.159375+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.118",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene SEMA3E from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:50.091001+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.118",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SEMA3E was added\ngene: SEMA3E was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Red,Expert Review\nMode of inheritance for gene: SEMA3E was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SEMA3E were set to 25985275\nPhenotypes for gene: SEMA3E were set to ?CHARGE syndrome (MIM#214800)",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:12:44.296166+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.117",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene SEMA3A from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:44.251376+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.117",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: SEMA3A was added\ngene: SEMA3A was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Green,Expert Review Green,Expert Review\nMode of inheritance for gene: SEMA3A was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal\nPublications for gene: SEMA3A were set to 28075028; 33369061; 20301509; 21059704; 24124006; 22927827\nPhenotypes for gene: SEMA3A were set to Hypogonadotropic hypogonadism 16 with or without anosmia - MIM#614897",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:12:37.903343+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.116",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene PROK2 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:37.853576+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.116",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: PROK2 was added\ngene: PROK2 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PROK2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: PROK2 were set to 18559922; 17054399; 17959774; 18285834\nPhenotypes for gene: PROK2 were set to Hypogonadotropic hypogonadism 4 with or without anosmia (MIM#610628)",
"entity_name": "PROK2",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:12:30.446870+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.115",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene PRDM13 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:30.373239+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.115",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: PRDM13 was added\ngene: PRDM13 was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Amber,Expert Review Amber,Literature\nfounder tags were added to gene: PRDM13.\nMode of inheritance for gene: PRDM13 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PRDM13 were set to 34730112\nPhenotypes for gene: PRDM13 were set to Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, MIM# 619761",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:12:23.746838+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.114",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene PLXNA3 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:23.678130+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.114",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: PLXNA3 was added\ngene: PLXNA3 was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Literature\nMode of inheritance for gene: PLXNA3 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: PLXNA3 were set to PMID: 33495532\nPhenotypes for gene: PLXNA3 were set to Hypogonadotropic hypogonadism",
"entity_name": "PLXNA3",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:12:17.182257+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.113",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene NSMF from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:17.107363+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.113",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: NSMF was added\ngene: NSMF was added to Pituitary hormone deficiency. Sources: Expert list,Expert Review Red,Expert Review Red,Expert list\nMode of inheritance for gene: NSMF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NSMF were set to 15362570; 17235395; 21700882\nPhenotypes for gene: NSMF were set to Hypogonadotropic hypogonadism 9 with or without anosmia, MIM#\t614838",
"entity_name": "NSMF",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:12:10.151949+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.112",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene NR0B1 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:10.073422+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.112",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: NR0B1 was added\ngene: NR0B1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green,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": "2025-12-11T11:12:02.734013+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.111",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene NHLH2 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:12:02.594735+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.111",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: NHLH2 was added\ngene: NHLH2 was added to Pituitary hormone deficiency. Sources: Expert Review,Expert Review Red,Expert Review Red,Expert Review\nMode of inheritance for gene: NHLH2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NHLH2 were set to 35066646\nPhenotypes for gene: NHLH2 were set to Hypogonadotropic hypogonadism 27 without anosmia , MIM#\t619755",
"entity_name": "NHLH2",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:11:55.891338+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.110",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene NDNF from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:11:55.811948+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.110",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: NDNF was added\ngene: NDNF was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Amber,Expert Review Amber,Literature\nMode of inheritance for gene: NDNF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NDNF were set to 31883645; 40788466\nPhenotypes for gene: NDNF were set to Hypogonadotropic hypogonadism 25 with anosmia MIM#618841",
"entity_name": "NDNF",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:11:46.793084+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.109",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene LHB from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:11:46.753933+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.109",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: LHB was added\ngene: LHB was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: LHB was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: LHB were set to 17761593; 28092701; 29476300; 22723313; 15602022\nPhenotypes for gene: LHB were set to Hypogonadotropic hypogonadism 23 with or without anosmia (MIM#228300)",
"entity_name": "LHB",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:11:39.912056+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.108",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene KLB from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:11:39.864908+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.108",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: KLB was added\ngene: KLB was added to Pituitary hormone deficiency. Sources: Literature,Expert Review Green,Expert Review Green,Literature\nMode of inheritance for gene: KLB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: KLB were set to 28754744\nPhenotypes for gene: KLB were set to Hypogonadotropic hypogonadism",
"entity_name": "KLB",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:11:33.993425+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.107",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene KISS1R from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:11:33.948688+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.107",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: KISS1R was added\ngene: KISS1R was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: KISS1R was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: KISS1R were set to 17164310; 31073722; 14573733\nPhenotypes for gene: KISS1R were set to Hypogonadotropic hypogonadism 8 with or without anosmia (MIM#614837)",
"entity_name": "KISS1R",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:11:30.659696+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.106",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene KISS1 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:11:30.595458+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.106",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: KISS1 was added\ngene: KISS1 was added to Pituitary hormone deficiency. Sources: Expert list,Expert Review Amber,Expert Review Amber,Expert list\nMode of inheritance for gene: KISS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: KISS1 were set to 22335740; 25783047; 22766261; 17563351\nPhenotypes for gene: KISS1 were set to Hypogonadotropic hypogonadism 13 with or without anosmia, MIM#\t614842",
"entity_name": "KISS1",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:11:18.514146+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.105",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene IL17RD from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:11:18.469230+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.105",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: IL17RD was added\ngene: IL17RD was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Red,Victorian Clinical Genetics Services\ndisputed tags were added to gene: IL17RD.\nMode of inheritance for gene: IL17RD was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: IL17RD were set to 23643382; 32389901\nPhenotypes for gene: IL17RD were set to Hypogonadotropic hypogonadism 18 with or without anosmia, MIM# 615267",
"entity_name": "IL17RD",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:11:05.588750+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.104",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene HS6ST1 from panel Hypogonadotropic hypogonadism",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T11:11:05.518204+11:00",
"panel_name": "Pituitary hormone deficiency",
"panel_id": 3236,
"panel_version": "0.104",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: HS6ST1 was added\ngene: HS6ST1 was added to Pituitary hormone deficiency. Sources: Victorian Clinical Genetics Services,Expert Review Red,Expert Review Red,Victorian Clinical Genetics Services\nMode of inheritance for gene: HS6ST1 was set to Other\nPublications for gene: HS6ST1 were set to 21700882\nPhenotypes for gene: HS6ST1 were set to {Hypogonadotropic hypogonadism 15 with or without anosmia} 614880",
"entity_name": "HS6ST1",
"entity_type": "gene"
},
{
"created": "2025-12-11T11:09:32.630328+11:00",
"panel_name": "Hypogonadotropic hypogonadism",
"panel_id": 4521,
"panel_version": "0.74",
"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": "2025-12-11T10:59:12.039291+11:00",
"panel_name": "Hypogonadotropic hypogonadism",
"panel_id": 4521,
"panel_version": "0.73",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "HPO terms changed from to Hypogonadotropic hypogonadism HP:0000044\nPanel status changed from internal to public\nPanel types changed to Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T10:55:34.201657+11:00",
"panel_name": "Hypogonadotropic hypogonadism",
"panel_id": 4521,
"panel_version": "0.72",
"user_name": "Chirag Patel",
"item_type": "panel",
"text": "Copied gene FEZF1 from panel Differences of Sex Development",
"entity_name": null,
"entity_type": null
},
{
"created": "2025-12-11T10:55:34.161476+11:00",
"panel_name": "Hypogonadotropic hypogonadism",
"panel_id": 4521,
"panel_version": "0.72",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FEZF1 was added\ngene: FEZF1 was added to Hypogonadotropic hypogonadism. Sources: Expert Review Amber,Victorian Clinical Genetics Services\nMode of inheritance for gene: FEZF1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FEZF1 were set to 25192046; 32400067\nPhenotypes for gene: FEZF1 were set to Hypogonadotropic hypogonadism 22, with or without anosmia 616030",
"entity_name": "FEZF1",
"entity_type": "gene"
}
]
}