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{
"count": 220423,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=793",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=791",
"results": [
{
"created": "2022-07-21T12:49:47.779439+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.58",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: C6: Rating: AMBER; Mode of pathogenicity: None; Publications: 31440263, 23537992, 17257682, 22668955, 32670577; Phenotypes: C6 deficiency (MIM#612446); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "C6",
"entity_type": "gene"
},
{
"created": "2022-07-21T12:38:43.812691+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.72",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: C5: Rating: AMBER; Mode of pathogenicity: None; Publications: 31440263, 23743184, 15488949, 15778377, 23371790; Phenotypes: C5 deficiency (MIM#609536); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "C5",
"entity_type": "gene"
},
{
"created": "2022-07-21T11:45:57.607601+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.114",
"user_name": "Peter McNaughton",
"item_type": "entity",
"text": "reviewed gene: IL23R: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 35829840; Phenotypes: Susceptibility to mycobacterial disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL23R",
"entity_type": "gene"
},
{
"created": "2022-07-21T11:37:40.442832+10:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "1.4",
"user_name": "Peter McNaughton",
"item_type": "entity",
"text": "reviewed gene: HYOU1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 35822684; Phenotypes: Severe congenital neutropaenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HYOU1",
"entity_type": "gene"
},
{
"created": "2022-07-21T11:32:14.817019+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.58",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: PGK1: Rating: ; Mode of pathogenicity: None; Publications: 16567715, 30887539, 22348148, 28580215; Phenotypes: Phosphoglycerate kinase 1 deficiency (MIM#300653); Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "PGK1",
"entity_type": "gene"
},
{
"created": "2022-07-21T11:02:35.303270+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.58",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: GK: Rating: AMBER; Mode of pathogenicity: None; Publications: 33212314, 16549535, 10851254, 9719371, 8651297; Phenotypes: Glycerol kinase deficiency (MIM#307030); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GK",
"entity_type": "gene"
},
{
"created": "2022-07-20T20:16:13.865365+10:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.284",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UROS were set to 24027798",
"entity_name": "UROS",
"entity_type": "gene"
},
{
"created": "2022-07-20T20:15:36.024783+10:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.283",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UROS as Green List (high evidence)",
"entity_name": "UROS",
"entity_type": "gene"
},
{
"created": "2022-07-20T20:15:36.016361+10:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.283",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uros has been classified as Green List (High Evidence).",
"entity_name": "UROS",
"entity_type": "gene"
},
{
"created": "2022-07-20T17:03:29.140536+10:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.282",
"user_name": "Chern Lim",
"item_type": "entity",
"text": "reviewed gene: UROS: Rating: GREEN; Mode of pathogenicity: None; Publications: 30685241, 34828434, 15065102, 11254675; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "UROS",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:59:09.356918+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: HERC2.",
"entity_name": "HERC2",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:57:43.938518+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: GBA.",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:54:52.406148+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SAMD9 as ready",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:54:52.395694+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: samd9 has been classified as Red List (Low Evidence).",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:54:09.497806+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SAMD9 were set to ",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:53:57.662216+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SAMD9 as Red List (low evidence)",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:53:57.648834+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: samd9 has been classified as Red List (Low Evidence).",
"entity_name": "SAMD9",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:53:11.312488+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: FTCD.",
"entity_name": "FTCD",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:51:19.705068+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT85 as ready",
"entity_name": "KRT85",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:51:19.695277+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt85 has been classified as Red List (Low Evidence).",
"entity_name": "KRT85",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:51:05.082060+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KRT85 as Red List (low evidence)",
"entity_name": "KRT85",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:51:05.064734+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt85 has been classified as Red List (Low Evidence).",
"entity_name": "KRT85",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:50:45.879176+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KRT85: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ectodermal dysplasia 4, hair/nail type (MIM#602032); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KRT85",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:40:10.930193+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAG2 as ready",
"entity_name": "RAG2",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:40:10.914296+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rag2 has been classified as Green List (High Evidence).",
"entity_name": "RAG2",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:40:05.311708+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAG2 were set to ",
"entity_name": "RAG2",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:38:38.128944+10:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PPP1R13L were changed from Dilated cardiomyopathy, onset in infancy to Multiple congenital anomalies/dysmorphic syndrome, MONDO:0019042 - PPP1R13L-related; Dilated cardiomyopathy, onset in infancy",
"entity_name": "PPP1R13L",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:38:08.830411+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PPP1R13L were changed from Dilated cardiomyopathy, onset in infancy to Multiple congenital anomalies/dysmorphic syndrome, MONDO:0019042 - PPP1R13L-related; Dilated cardiomyopathy, onset in infancy",
"entity_name": "PPP1R13L",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:37:41.598976+10:00",
"panel_name": "Clefting disorders",
"panel_id": 3368,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PPP1R13L were changed from Dilated cardiomyopathy, onset in infancy; Cleft lip and palate to Multiple congenital anomalies/dysmorphic syndrome, MONDO:0019042 - PPP1R13L-related; Dilated cardiomyopathy, onset in infancy; Cleft lip and palate",
"entity_name": "PPP1R13L",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:37:18.494702+10:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PPP1R13L were changed from Dilated cardiomyopathy, onset in infancy; Cleft lip and palate to Multiple congenital anomalies/dysmorphic syndrome, MONDO:0019042 - PPP1R13L-related; Dilated cardiomyopathy, onset in infancy; Cleft lip and palate",
"entity_name": "PPP1R13L",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:36:35.257653+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: CARD9.",
"entity_name": "CARD9",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:34:15.709717+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: PLG.",
"entity_name": "PLG",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:32:49.878745+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: GYS2.",
"entity_name": "GYS2",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:30:56.161921+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: MPZ.",
"entity_name": "MPZ",
"entity_type": "gene"
},
{
"created": "2022-07-20T16:27:53.271183+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: KIAA1161.",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2022-07-20T14:05:51.362974+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: HERC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 31124564, 11896453; Phenotypes: Intellectual developmental disorder, autosomal recessive 38 (MIM#615516); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HERC2",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:38:23.644132+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: GBA: Rating: AMBER; Mode of pathogenicity: None; Publications: 28727984; Phenotypes: Gaucher disease, perinatal lethal (MIM#608013); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:28:43.554622+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIAA1161 as ready",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:28:43.543571+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kiaa1161 has been classified as Green List (High Evidence).",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:28:11.331040+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIAA1161 were changed from Primary familial brain calcification; Atypical parkinsonism; Supranuclear gaze palsy; OMIM 618317 to Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM #618317; Primary familial brain calcification; Atypical parkinsonism; Supranuclear gaze palsy",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:27:23.028606+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIAA1161 were set to PMID: 32211515",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:26:28.380583+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.213",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIAA1161 as Green List (high evidence)",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:26:28.368358+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.213",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kiaa1161 has been classified as Green List (High Evidence).",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:25:52.750983+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIAA1161: Rating: GREEN; Mode of pathogenicity: None; Publications: 30656188, 30649222, 30460687, 29910000, 31951047; Phenotypes: Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM #618317; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:23:27.107992+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NHLRC1 as ready",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:23:27.092637+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nhlrc1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:23:24.409506+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NHLRC1 were changed from Lafora disease; Progressive Myoclonic Epilepsy; Parkinsonism; OMIM 254780 to Epilepsy, progressive myoclonic 2B (Lafora), MIM# 254780; Lafora disease; Progressive Myoclonic Epilepsy; Parkinsonism",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:22:36.353988+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.211",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NHLRC1 as Amber List (moderate evidence)",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:22:36.341901+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.211",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nhlrc1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:22:03.476227+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NHLRC1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Epilepsy, progressive myoclonic 2B (Lafora), MIM# 254780; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NHLRC1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:19:05.523286+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: C9orf3.",
"entity_name": "C9orf3",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:18:37.761691+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: C9orf3 as ready",
"entity_name": "C9orf3",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:18:37.752554+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: c9orf3 has been classified as Green List (High Evidence).",
"entity_name": "C9orf3",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:18:30.728203+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: C9orf3 were changed from Dystonia-31; Childhood/Adolescence onset generalised dystonia; Dystonia parkinsonism; Zech-Boesch Syndrome; OMIM 619565 to Dystonia 31, MIM# 619565; Childhood/Adolescence onset generalised dystonia; Dystonia parkinsonism; Zech-Boesch Syndrome",
"entity_name": "C9orf3",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:17:40.153527+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: C9orf3 as Green List (high evidence)",
"entity_name": "C9orf3",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:17:40.142368+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: c9orf3 has been classified as Green List (High Evidence).",
"entity_name": "C9orf3",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:17:07.047635+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: C9orf3: Rating: GREEN; Mode of pathogenicity: None; Publications: 35306330; Phenotypes: Dystonia 31, MIM# 619565; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "C9orf3",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:13:05.253436+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: NCF1.",
"entity_name": "NCF1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:12:31.290002+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: NEB.",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:11:58.043599+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: HYDIN.",
"entity_name": "HYDIN",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:10:33.919518+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SNORD118 as ready",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:10:33.907833+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: snord118 has been classified as Red List (Low Evidence).",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:10:23.907011+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SNORD118 were set to ",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:10:07.891157+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SNORD118 as Red List (low evidence)",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:10:07.882096+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: snord118 has been classified as Red List (Low Evidence).",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:09:54.336477+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SNORD118: Rating: RED; Mode of pathogenicity: None; Publications: 32361877, 33029936; Phenotypes: Leukoencephalopathy, brain calcifications, and cysts, MIM#614561; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:07:29.719424+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBA1 as ready",
"entity_name": "UBA1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:07:29.710035+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uba1 has been classified as Green List (High Evidence).",
"entity_name": "UBA1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:05:51.392834+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBA1 were set to ",
"entity_name": "UBA1",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:03:12.408342+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: CHM.",
"entity_name": "CHM",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:01:39.974721+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: PROC.",
"entity_name": "PROC",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:00:20.525240+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IKBKG as ready",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2022-07-20T13:00:20.516753+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ikbkg has been classified as Amber List (Moderate Evidence).",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:59:59.661082+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IKBKG as Amber List (moderate evidence)",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:59:59.648621+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ikbkg has been classified as Amber List (Moderate Evidence).",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:59:44.299858+10:00",
"panel_name": "Reproductive Carrier Screen_VCGS",
"panel_id": 3861,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IKBKG: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:58:23.087081+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATXN10 as ready",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:58:23.077708+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atxn10 has been removed from the panel.",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:58:18.359501+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag STR tag was added to gene: ATXN10.",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:57:57.552499+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: ATXN10",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:57:15.048559+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATXN2 as ready",
"entity_name": "ATXN2",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:57:15.029374+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atxn2 has been removed from the panel.",
"entity_name": "ATXN2",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:57:04.571716+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ATXN2 were set to PMID: 11761482, 17923635",
"entity_name": "ATXN2",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:56:30.927675+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag STR tag was added to gene: ATXN2.",
"entity_name": "ATXN2",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:56:16.823831+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: ATXN2",
"entity_name": "ATXN2",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:55:38.006561+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag STR tag was added to gene: ATXN3.",
"entity_name": "ATXN3",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:55:31.703956+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATXN3 as ready",
"entity_name": "ATXN3",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:55:31.694978+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atxn3 has been removed from the panel.",
"entity_name": "ATXN3",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:55:22.153376+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: ATXN3",
"entity_name": "ATXN3",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:54:18.772449+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATXN8 as ready",
"entity_name": "ATXN8",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:54:18.761108+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atxn8 has been removed from the panel.",
"entity_name": "ATXN8",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:54:12.092619+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag STR tag was added to gene: ATXN8.",
"entity_name": "ATXN8",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:54:02.194206+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: ATXN8",
"entity_name": "ATXN8",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:52:22.493699+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TPP1 as ready",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:52:22.485238+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpp1 has been classified as Green List (High Evidence).",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:52:19.335176+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TPP1 were changed from Late Infantile NCL; Parkinsonism; OMIM 204500 to Ceroid lipofuscinosis, neuronal, 2, MIM# 204500; Parkinsonism",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:51:38.081844+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TPP1 as Green List (high evidence)",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:51:38.064511+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpp1 has been classified as Green List (High Evidence).",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:51:05.197983+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.205",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TPP1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 2, MIM# 204500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2022-07-20T12:49:37.320608+10:00",
"panel_name": "Early-onset Parkinson disease",
"panel_id": 26,
"panel_version": "0.205",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP27A1 as ready",
"entity_name": "CYP27A1",
"entity_type": "gene"
}
]
}