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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=703",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=701",
"results": [
{
"created": "2022-11-03T07:55:42.525589+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: CXCR4.",
"entity_name": "CXCR4",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:55:29.117506+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CXCR4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: WHIM syndrome, MIM# 193670; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CXCR4",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:53:15.887287+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYBA as ready",
"entity_name": "CYBA",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:53:15.838369+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyba has been classified as Green List (High Evidence).",
"entity_name": "CYBA",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:53:07.437018+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: CYBA.",
"entity_name": "CYBA",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:52:58.514918+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYBA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Chronic granulomatous disease 4, autosomal recessive, MIM# 233690; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYBA",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:50:51.949569+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYBB as ready",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:50:51.939275+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cybb has been classified as Green List (High Evidence).",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:50:38.923660+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: CYBB.",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:50:30.020577+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYBB: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Chronic granulomatous disease, X-linked, MIM# 306400; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "CYBB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:47:17.600063+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP4F22 as ready",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:47:17.585446+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp4f22 has been classified as Red List (Low Evidence).",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:47:11.066900+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP4F22 were changed from Ichthyosis, congenital, autosomal recessive to Ichthyosis, congenital, autosomal recessive 5, MIM# 604777",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:46:57.229568+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CYP4F22 as Red List (low evidence)",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:46:57.221014+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp4f22 has been classified as Red List (Low Evidence).",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:46:46.369907+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP4F22: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ichthyosis, congenital, autosomal recessive 5, MIM# 604777; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:44:37.236109+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMAB as ready",
"entity_name": "MMAB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:44:37.224950+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmab has been classified as Green List (High Evidence).",
"entity_name": "MMAB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:42:39.752740+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IVD as ready",
"entity_name": "IVD",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:42:39.744162+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ivd has been classified as Green List (High Evidence).",
"entity_name": "IVD",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:41:33.598961+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GBA as ready",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:41:33.589737+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gba has been classified as Green List (High Evidence).",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:41:30.189581+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GBA were changed from Gaucher disease 1 to Gaucher disease type 1, MIM#230800",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:41:17.582870+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: GBA.",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:40:10.370293+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: G6PC3.",
"entity_name": "G6PC3",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:40:02.106212+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: G6PC3 as ready",
"entity_name": "G6PC3",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:40:02.088646+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: g6pc3 has been classified as Green List (High Evidence).",
"entity_name": "G6PC3",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:38:09.399515+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CREBBP as ready",
"entity_name": "CREBBP",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:38:09.386731+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crebbp has been classified as Red List (Low Evidence).",
"entity_name": "CREBBP",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:38:04.333332+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CREBBP were changed from Rubinstein-Taybi syndrome to Rubinstein-Taybi syndrome 1, MIM# 180849; Menke-Hennekam syndrome 1, MIM# 618332",
"entity_name": "CREBBP",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:37:51.929655+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.781",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CREBBP as Red List (low evidence)",
"entity_name": "CREBBP",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:37:51.919726+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.781",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crebbp has been classified as Red List (Low Evidence).",
"entity_name": "CREBBP",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:37:41.205674+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CREBBP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Rubinstein-Taybi syndrome 1, MIM# 180849, Menke-Hennekam syndrome 1, MIM# 618332; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CREBBP",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:35:45.892291+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL1A2 as ready",
"entity_name": "COL1A2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:35:45.883846+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col1a2 has been classified as Green List (High Evidence).",
"entity_name": "COL1A2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:35:41.995926+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL1A2 were changed from Osteogenesis imperfecta, type II to Osteogenesis imperfecta, type II , MIM#166210",
"entity_name": "COL1A2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:35:24.306669+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COL1A2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Osteogenesis imperfecta, type II , MIM#166210; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "COL1A2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:30:49.538377+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL1A1 as ready",
"entity_name": "COL1A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:30:49.529583+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col1a1 has been classified as Green List (High Evidence).",
"entity_name": "COL1A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:30:45.724746+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL1A1 were changed from Osteogenesis imperfecta, type I to Osteogenesis imperfecta, type I, MIM#166200",
"entity_name": "COL1A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:30:31.200398+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: COL1A1.",
"entity_name": "COL1A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:30:19.574708+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COL1A1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Osteogenesis imperfecta, type I MIM#166200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "COL1A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:27:18.181694+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL17A1 as ready",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:27:18.161464+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col17a1 has been classified as Red List (Low Evidence).",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:27:14.656880+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL17A1 were changed from Epidermolysis bullosa, junctional, non-Herlitz type to Epidermolysis bullosa, junctional 4, intermediate MIM#619787",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:26:57.005009+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COL17A1 as Red List (low evidence)",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:26:56.995290+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col17a1 has been classified as Red List (Low Evidence).",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:26:45.301535+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COL17A1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Epidermolysis bullosa, junctional 4, intermediate MIM#619787; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:24:38.886666+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHYH as ready",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:24:38.878139+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phyh has been classified as Red List (Low Evidence).",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:24:34.463923+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PHYH were changed from Refsum disease to Refsum disease, MIM# 266500",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:24:25.069020+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PHYH as Red List (low evidence)",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:24:25.058588+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phyh has been classified as Red List (Low Evidence).",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:24:12.538335+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PHYH.",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:23:27.238608+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHKG2 as ready",
"entity_name": "PHKG2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:23:27.229032+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phkg2 has been classified as Green List (High Evidence).",
"entity_name": "PHKG2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:23:23.864510+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PHKG2 were changed from Phosphorylase kinase deficiency to Glycogen storage disease IXc, MIM# 613027",
"entity_name": "PHKG2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:23:12.232681+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PHKG2.",
"entity_name": "PHKG2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:22:28.093677+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHKB as ready",
"entity_name": "PHKB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:22:28.083495+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phkb has been classified as Green List (High Evidence).",
"entity_name": "PHKB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:22:24.539114+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PHKB were changed from Phosphorylase kinase deficiency to Phosphorylase kinase deficiency of liver and muscle, autosomal recessive 261750; Glycogen storage disease IXb, MONDO:0009868",
"entity_name": "PHKB",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:21:43.597198+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHKA2 as ready",
"entity_name": "PHKA2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:21:43.588896+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phka2 has been classified as Green List (High Evidence).",
"entity_name": "PHKA2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:21:29.947263+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PHKA2 were set to ",
"entity_name": "PHKA2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:21:08.152929+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PHKA2 were changed from Phosphorylase kinase deficiency to Glycogen storage disease, type IXa1 and a2, MIM# 306000",
"entity_name": "PHKA2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:20:30.936823+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHGDH as ready",
"entity_name": "PHGDH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:20:30.919751+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phgdh has been classified as Green List (High Evidence).",
"entity_name": "PHGDH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:20:24.614903+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PHGDH.",
"entity_name": "PHGDH",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:18:47.388073+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGM1 as ready",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:18:47.378699+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgm1 has been classified as Green List (High Evidence).",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:18:22.311778+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PGM1.",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:17:24.663845+11:00",
"panel_name": "Rhabdomyolysis",
"panel_id": 3084,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PGM1.",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:16:55.191573+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PGM1.",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:16:31.816902+11:00",
"panel_name": "Glycogen Storage Diseases",
"panel_id": 106,
"panel_version": "1.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PGM1.",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:16:15.448909+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "1.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PGM1.",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:15:43.847435+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: PGM1.",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:14:57.649636+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PFKM as ready",
"entity_name": "PFKM",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:14:57.640163+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pfkm has been classified as Red List (Low Evidence).",
"entity_name": "PFKM",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:14:47.892151+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PFKM were changed from Glycogen storage disease 7 to Glycogen storage disease VII (MIM#232800)",
"entity_name": "PFKM",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:14:27.372354+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.769",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PFKM were set to ",
"entity_name": "PFKM",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:14:12.756700+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.768",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PFKM as Red List (low evidence)",
"entity_name": "PFKM",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:14:12.748590+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.768",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pfkm has been classified as Red List (Low Evidence).",
"entity_name": "PFKM",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:13:21.121474+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX7 as ready",
"entity_name": "PEX7",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:13:21.110781+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex7 has been classified as Red List (Low Evidence).",
"entity_name": "PEX7",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:13:17.477741+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX7 were changed from Rhizomelic chondrodysplasia punctata; Refsum disease to Peroxisome biogenesis disorder 9B, MIM# 614879; Rhizomelic chondrodysplasia punctata, type 1, MIM# 215100",
"entity_name": "PEX7",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:12:48.693746+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.766",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX7 as Red List (low evidence)",
"entity_name": "PEX7",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:12:48.684838+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.766",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex7 has been classified as Red List (Low Evidence).",
"entity_name": "PEX7",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:11:59.750851+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX6 as ready",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:11:59.739715+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex6 has been classified as Red List (Low Evidence).",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:11:56.238032+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX6 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 4A (Zellweger) (MIM#614862)",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:11:38.073746+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.764",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX6 as Red List (low evidence)",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:11:38.065318+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.764",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex6 has been classified as Red List (Low Evidence).",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:11:08.751588+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.763",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX5 as ready",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:11:08.741724+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.763",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex5 has been classified as Red List (Low Evidence).",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:11:03.855171+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.763",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX5 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 10A (Zellweger) 614882",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:10:54.211659+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.762",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX5 as Red List (low evidence)",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:10:54.203559+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.762",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex5 has been classified as Red List (Low Evidence).",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:10:12.569168+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX3 as ready",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:10:12.561327+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex3 has been classified as Red List (Low Evidence).",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:10:08.795159+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX3 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 10A (Zellweger) 614882",
"entity_name": "PEX3",
"entity_type": "gene"
}
]
}