{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1034","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1032","results":[{"created":"2022-01-21T09:20:32.726398+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10711","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MSTO1 were changed from  to Myopathy, mitochondrial, and ataxia, OMIM:617675; Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome, MONDO:0044714","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:20:10.574023+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10710","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MSTO1 were set to ","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:20:02.998705+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10709","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MSTO1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:19:38.459090+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10708","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MSTO1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28554942, 28544275, 31604776, 31463572, 31130378, 30684668, 29339779; Phenotypes: Myopathy, mitochondrial, and ataxia, OMIM:617675, Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome, MONDO:0044714; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:17:49.709070+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2626","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MSTO1 as ready","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:17:49.700287+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2626","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: msto1 has been classified as Green List (High Evidence).","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:17:44.556983+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2626","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MSTO1 were set to 28544275; 29339779; 31130378; 31604776; 28554942","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:17:09.761756+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2625","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MSTO1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:16:58.526493+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2624","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MSTO1 as Green List (high evidence)","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:16:58.514713+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2624","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: msto1 has been classified as Green List (High Evidence).","entity_name":"MSTO1","entity_type":"gene"},{"created":"2022-01-21T09:16:14.750086+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2623","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MED13L as ready","entity_name":"MED13L","entity_type":"gene"},{"created":"2022-01-21T09:16:14.739465+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2623","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: med13l has been classified as Green List (High Evidence).","entity_name":"MED13L","entity_type":"gene"},{"created":"2022-01-21T09:16:04.732281+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2623","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MED13L were changed from INTELLECTUAL DISABILITY to Impaired intellectual development and distinctive facial features with or without cardiac defects MIM#616789","entity_name":"MED13L","entity_type":"gene"},{"created":"2022-01-21T09:15:49.949795+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2622","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MED13L were set to ","entity_name":"MED13L","entity_type":"gene"},{"created":"2022-01-21T09:15:36.130625+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2621","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MED13L was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MED13L","entity_type":"gene"},{"created":"2022-01-21T09:15:19.689464+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2620","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MED13L as Green List (high evidence)","entity_name":"MED13L","entity_type":"gene"},{"created":"2022-01-21T09:15:19.678547+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2620","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: med13l has been classified as Green List (High Evidence).","entity_name":"MED13L","entity_type":"gene"},{"created":"2022-01-21T09:15:03.423035+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2619","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MED13L: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Impaired intellectual development and distinctive facial features with or without cardiac defects MIM#616789; Mode of inheritance: None","entity_name":"MED13L","entity_type":"gene"},{"created":"2022-01-21T09:13:41.278348+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2619","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MECR as ready","entity_name":"MECR","entity_type":"gene"},{"created":"2022-01-21T09:13:41.268789+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2619","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mecr has been classified as Red List (Low Evidence).","entity_name":"MECR","entity_type":"gene"},{"created":"2022-01-21T09:13:35.809566+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2619","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MECR were changed from Childhood-Onset Dystonia and Optic Atrophy to Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities, MIM#\t617282","entity_name":"MECR","entity_type":"gene"},{"created":"2022-01-21T09:13:09.556704+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2618","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MECR were set to ","entity_name":"MECR","entity_type":"gene"},{"created":"2022-01-21T09:12:57.329991+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2617","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MECR as Red List (low evidence)","entity_name":"MECR","entity_type":"gene"},{"created":"2022-01-21T09:12:57.320391+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2617","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mecr has been classified as Red List (Low Evidence).","entity_name":"MECR","entity_type":"gene"},{"created":"2022-01-21T09:11:28.852563+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2616","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MECOM as ready","entity_name":"MECOM","entity_type":"gene"},{"created":"2022-01-21T09:11:28.838319+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2616","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mecom has been classified as Green List (High Evidence).","entity_name":"MECOM","entity_type":"gene"},{"created":"2022-01-21T09:11:24.521233+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2616","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MECOM were changed from Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia to Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 MIM#616738","entity_name":"MECOM","entity_type":"gene"},{"created":"2022-01-21T09:11:08.264796+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2615","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MECOM were set to ","entity_name":"MECOM","entity_type":"gene"},{"created":"2022-01-21T09:10:47.568392+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2614","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MECOM was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MECOM","entity_type":"gene"},{"created":"2022-01-21T09:10:33.581197+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2613","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MECOM as Green List (high evidence)","entity_name":"MECOM","entity_type":"gene"},{"created":"2022-01-21T09:10:33.570787+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2613","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mecom has been classified as Green List (High Evidence).","entity_name":"MECOM","entity_type":"gene"},{"created":"2022-01-21T09:09:32.714007+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4454","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MDH2 as ready","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:09:32.704419+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4454","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mdh2 has been classified as Green List (High Evidence).","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:09:25.213481+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4454","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MDH2 were changed from  to Developmental and epileptic encephalopathy 51 MIM#617339","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:08:43.723068+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4453","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MDH2 were set to ","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:08:16.072695+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4452","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MDH2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:07:40.589048+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4451","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MDH2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27989324, 34766628; Phenotypes: Developmental and epileptic encephalopathy 51 MIM#617339; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:06:59.884935+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1425","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MDH2 as ready","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:06:59.873835+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1425","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mdh2 has been classified as Green List (High Evidence).","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:06:56.720389+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1425","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MDH2 were changed from  to Developmental and epileptic encephalopathy 51 MIM#617339","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:06:14.244554+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1424","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MDH2 were set to ","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:05:43.915939+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1423","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MDH2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:04:54.841507+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1422","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MDH2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27989324, 34766628; Phenotypes: Developmental and epileptic encephalopathy 51 MIM#617339; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:03:37.046956+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2612","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MDH2 as ready","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:03:37.036298+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2612","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mdh2 has been classified as Red List (Low Evidence).","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:03:31.800459+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2612","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MDH2 were changed from Early-Onset Severe Encephalopathy to Developmental and epileptic encephalopathy 51 MIM#617339","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T09:03:04.430322+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2611","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MDH2 were set to ","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T08:56:09.524448+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2610","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MDH2 as Red List (low evidence)","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T08:56:09.512339+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2610","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mdh2 has been classified as Red List (Low Evidence).","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T08:55:28.483490+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10708","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MDH2 as ready","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T08:55:28.473131+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10708","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mdh2 has been classified as Green List (High Evidence).","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T08:55:18.363818+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10708","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MDH2 were changed from  to Developmental and epileptic encephalopathy 51 MIM#617339","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T08:54:28.249196+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10707","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MDH2 were set to ","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T08:54:01.910445+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10706","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MDH2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MDH2","entity_type":"gene"},{"created":"2022-01-21T08:53:19.762563+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10705","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXH1 as ready","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:53:19.746888+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10705","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxh1 has been classified as Amber List (Moderate Evidence).","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:53:09.232650+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10705","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXH1 were changed from  to Congenital heart disease; holoprosencephaly","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:52:48.369928+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10704","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXH1 were set to ","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:52:26.819062+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10703","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FOXH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:52:06.802631+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10702","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FOXH1 as Amber List (moderate evidence)","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:52:06.793832+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10702","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxh1 has been classified as Amber List (Moderate Evidence).","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:51:35.175565+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXH1 as ready","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:51:35.165950+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxh1 has been classified as Amber List (Moderate Evidence).","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:51:32.601539+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXH1 were changed from  to Congenital heart disease","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:51:08.763424+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXH1 were set to ","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:50:38.236514+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FOXH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:50:09.076248+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FOXH1 as Amber List (moderate evidence)","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:50:09.064582+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxh1 has been classified as Amber List (Moderate Evidence).","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:49:33.462400+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2609","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXH1 as ready","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:49:33.452212+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2609","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxh1 has been classified as Amber List (Moderate Evidence).","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:49:24.536690+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2609","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXH1 were set to 19933292; 18538293; 19525021","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:49:00.328163+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2608","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FOXH1 as Amber List (moderate evidence)","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:49:00.310674+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2608","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxh1 has been classified as Amber List (Moderate Evidence).","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:48:47.569973+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2607","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FOXH1: Changed rating: AMBER","entity_name":"FOXH1","entity_type":"gene"},{"created":"2022-01-21T08:46:45.194462+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10701","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MBOAT7 as ready","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:46:45.181164+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10701","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mboat7 has been classified as Green List (High Evidence).","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:46:35.060276+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10701","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MBOAT7 were changed from  to intellectual disability MIM#617188","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:46:11.912648+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10700","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MBOAT7 were set to ","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:45:49.457002+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10699","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MBOAT7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:41:03.538129+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2607","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MBOAT7 as ready","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:41:03.521951+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2607","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mboat7 has been classified as Amber List (Moderate Evidence).","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:40:58.897598+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2607","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MBOAT7 were changed from Intellectual Disability Accompanied by Epilepsy and Autistic Features to Intellectual disability MIM#617188","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:40:40.874793+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2606","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MBOAT7 were set to ","entity_name":"MBOAT7","entity_type":"gene"},{"created":"2022-01-21T08:39:12.345065+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2605","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAT1A as ready","entity_name":"MAT1A","entity_type":"gene"},{"created":"2022-01-21T08:39:12.335638+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2605","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mat1a has been classified as Red List (Low Evidence).","entity_name":"MAT1A","entity_type":"gene"},{"created":"2022-01-21T08:39:06.737815+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2605","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MAT1A was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MAT1A","entity_type":"gene"},{"created":"2022-01-21T08:38:50.265154+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2604","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAT1A were changed from METHIONINE ADENOSYLTRANSFERASE DEFICIENCY to Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency MIM#250850; Methionine adenosyltransferase deficiency, autosomal recessive MIM#250850; Disorders of the metabolism of sulphur amino acids","entity_name":"MAT1A","entity_type":"gene"},{"created":"2022-01-21T08:38:36.422062+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2603","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAT1A were set to ","entity_name":"MAT1A","entity_type":"gene"},{"created":"2022-01-21T08:37:46.208949+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2602","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAT1A as Red List (low evidence)","entity_name":"MAT1A","entity_type":"gene"},{"created":"2022-01-21T08:37:46.194878+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2602","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mat1a has been classified as Red List (Low Evidence).","entity_name":"MAT1A","entity_type":"gene"},{"created":"2022-01-21T08:36:55.709208+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2601","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAP3K7 as ready","entity_name":"MAP3K7","entity_type":"gene"},{"created":"2022-01-21T08:36:55.697803+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2601","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: map3k7 has been classified as Green List (High Evidence).","entity_name":"MAP3K7","entity_type":"gene"},{"created":"2022-01-21T08:36:50.147961+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2601","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAP3K7 were set to ","entity_name":"MAP3K7","entity_type":"gene"},{"created":"2022-01-21T08:36:29.745835+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2600","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MAP3K7 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAP3K7","entity_type":"gene"},{"created":"2022-01-21T08:36:14.206826+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2599","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAP3K7 as Green List (high evidence)","entity_name":"MAP3K7","entity_type":"gene"},{"created":"2022-01-21T08:36:14.196090+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2599","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: map3k7 has been classified as Green List (High Evidence).","entity_name":"MAP3K7","entity_type":"gene"},{"created":"2022-01-21T08:34:36.633374+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2598","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAP3K20 as ready","entity_name":"MAP3K20","entity_type":"gene"},{"created":"2022-01-21T08:34:36.623605+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2598","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: map3k20 has been classified as Green List (High Evidence).","entity_name":"MAP3K20","entity_type":"gene"},{"created":"2022-01-21T08:34:26.576285+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2598","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAP3K20 as Green List (high evidence)","entity_name":"MAP3K20","entity_type":"gene"},{"created":"2022-01-21T08:34:26.565242+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2598","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: map3k20 has been classified as Green List (High Evidence).","entity_name":"MAP3K20","entity_type":"gene"}]}