{"count":220790,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=997","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=995","results":[{"created":"2022-02-13T20:17:37.827020+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3371","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAN1B1 as Red List (low evidence)","entity_name":"MAN1B1","entity_type":"gene"},{"created":"2022-02-13T20:17:37.817586+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3371","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: man1b1 has been classified as Red List (Low Evidence).","entity_name":"MAN1B1","entity_type":"gene"},{"created":"2022-02-13T20:17:22.170314+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3370","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: MAN1B1: Clinical presentation is typically post-natal.","entity_name":"MAN1B1","entity_type":"gene"},{"created":"2022-02-13T20:17:08.693902+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3370","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MAN1B1: Changed rating: RED; Changed phenotypes: Rafiq syndrome, MIM# 614202","entity_name":"MAN1B1","entity_type":"gene"},{"created":"2022-02-13T20:16:12.625614+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3370","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MACF1 as ready","entity_name":"MACF1","entity_type":"gene"},{"created":"2022-02-13T20:16:12.612625+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3370","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: macf1 has been classified as Green List (High Evidence).","entity_name":"MACF1","entity_type":"gene"},{"created":"2022-02-13T20:16:06.574862+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3370","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: MACF1 was changed from  to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"MACF1","entity_type":"gene"},{"created":"2022-02-13T20:15:45.856063+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3369","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MACF1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MACF1","entity_type":"gene"},{"created":"2022-02-13T20:15:24.612194+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3368","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MACF1 as Green List (high evidence)","entity_name":"MACF1","entity_type":"gene"},{"created":"2022-02-13T20:15:24.600481+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3368","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: macf1 has been classified as Green List (High Evidence).","entity_name":"MACF1","entity_type":"gene"},{"created":"2022-02-13T20:14:37.707305+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3367","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRRC56 as ready","entity_name":"LRRC56","entity_type":"gene"},{"created":"2022-02-13T20:14:37.696632+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3367","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrrc56 has been classified as Green List (High Evidence).","entity_name":"LRRC56","entity_type":"gene"},{"created":"2022-02-13T20:14:30.292455+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3367","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LRRC56 as Green List (high evidence)","entity_name":"LRRC56","entity_type":"gene"},{"created":"2022-02-13T20:14:30.281029+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3367","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrrc56 has been classified as Green List (High Evidence).","entity_name":"LRRC56","entity_type":"gene"},{"created":"2022-02-13T20:13:54.092352+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3366","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRBA as ready","entity_name":"LRBA","entity_type":"gene"},{"created":"2022-02-13T20:13:54.081274+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3366","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrba has been classified as Red List (Low Evidence).","entity_name":"LRBA","entity_type":"gene"},{"created":"2022-02-13T20:13:42.308725+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3366","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRBA were changed from CHILDHOOD-ONSET HYPOGAMMAGLOBULINEMIA to Immunodeficiency, common variable, 8, with autoimmunity MIM#614700","entity_name":"LRBA","entity_type":"gene"},{"created":"2022-02-13T20:13:12.928242+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3365","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LRBA as Red List (low evidence)","entity_name":"LRBA","entity_type":"gene"},{"created":"2022-02-13T20:13:12.918301+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3365","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrba has been classified as Red List (Low Evidence).","entity_name":"LRBA","entity_type":"gene"},{"created":"2022-02-13T20:12:52.657178+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3364","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LRBA: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Immunodeficiency, common variable, 8, with autoimmunity MIM#614700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LRBA","entity_type":"gene"},{"created":"2022-02-13T20:11:36.506208+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3364","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LONP1 as ready","entity_name":"LONP1","entity_type":"gene"},{"created":"2022-02-13T20:11:36.494610+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3364","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lonp1 has been classified as Green List (High Evidence).","entity_name":"LONP1","entity_type":"gene"},{"created":"2022-02-13T20:11:24.276478+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3364","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LONP1 were set to ","entity_name":"LONP1","entity_type":"gene"},{"created":"2022-02-13T20:10:59.157904+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3363","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LONP1 as Green List (high evidence)","entity_name":"LONP1","entity_type":"gene"},{"created":"2022-02-13T20:10:59.147919+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3363","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lonp1 has been classified as Green List (High Evidence).","entity_name":"LONP1","entity_type":"gene"},{"created":"2022-02-13T20:10:12.653911+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3362","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: At least three unrelated cases described in the literature, ID is part of the phenotype.; to: At least three unrelated cases described in the literature, multiple congenital anomalies are part of the phenotype.","entity_name":"LONP1","entity_type":"gene"},{"created":"2022-02-13T20:08:51.961561+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3362","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIPT2 as ready","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-02-13T20:08:51.939438+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3362","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lipt2 has been classified as Red List (Low Evidence).","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-02-13T20:08:48.306873+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3362","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIPT2 were changed from Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy to Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, MIM#617668","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-02-13T20:08:25.985617+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3361","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIPT2 were set to ","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-02-13T20:08:09.762463+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3360","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LIPT2 as Red List (low evidence)","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-02-13T20:08:09.749948+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3360","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lipt2 has been classified as Red List (Low Evidence).","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-02-13T20:07:56.957840+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3359","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Three individuals from two unrelated families; profound ID. \nSources: Expert list; to: Three individuals from two unrelated families; onset is typically post-natal, though brain abnormalities reported in some.\r\nSources: Expert list","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-02-13T20:07:35.807148+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3359","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LIPT2: Changed rating: RED","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-02-13T20:06:15.056242+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3359","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIPT1 as ready","entity_name":"LIPT1","entity_type":"gene"},{"created":"2022-02-13T20:06:15.027329+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3359","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lipt1 has been classified as Red List (Low Evidence).","entity_name":"LIPT1","entity_type":"gene"},{"created":"2022-02-13T20:06:10.941243+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3359","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIPT1 were changed from Leigh syndrome with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase. to Lipoyltransferase 1 deficiency, MIM#616299","entity_name":"LIPT1","entity_type":"gene"},{"created":"2022-02-13T20:05:57.303716+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3358","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIPT1 were set to ","entity_name":"LIPT1","entity_type":"gene"},{"created":"2022-02-13T20:05:41.903247+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3357","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LIPT1 as Red List (low evidence)","entity_name":"LIPT1","entity_type":"gene"},{"created":"2022-02-13T20:05:41.892865+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3357","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lipt1 has been classified as Red List (Low Evidence).","entity_name":"LIPT1","entity_type":"gene"},{"created":"2022-02-13T20:05:17.110997+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3356","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Cognitive development is affected in this metabolic condition.; to: Clinical presentation is typically post-natal.","entity_name":"LIPT1","entity_type":"gene"},{"created":"2022-02-13T20:05:01.803476+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3356","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LIPT1: Changed rating: RED","entity_name":"LIPT1","entity_type":"gene"},{"created":"2022-02-13T18:32:29.418138+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3356","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIAS as ready","entity_name":"LIAS","entity_type":"gene"},{"created":"2022-02-13T18:32:29.406412+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3356","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lias has been classified as Red List (Low Evidence).","entity_name":"LIAS","entity_type":"gene"},{"created":"2022-02-13T18:32:26.296471+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3356","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIAS were changed from Neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation to Hyperglycinemia, lactic acidosis, and seizures, MIM#614462","entity_name":"LIAS","entity_type":"gene"},{"created":"2022-02-13T18:32:14.341998+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3355","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIAS were set to ","entity_name":"LIAS","entity_type":"gene"},{"created":"2022-02-13T18:32:01.535398+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3354","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LIAS as Red List (low evidence)","entity_name":"LIAS","entity_type":"gene"},{"created":"2022-02-13T18:32:01.516200+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3354","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lias has been classified as Red List (Low Evidence).","entity_name":"LIAS","entity_type":"gene"},{"created":"2022-02-13T18:31:45.881893+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3353","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: At least three families reported, severe ID is part of the phenotype.; to: At least three families reported, clinical presentation is typically post-natal.","entity_name":"LIAS","entity_type":"gene"},{"created":"2022-02-13T18:31:32.426663+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3353","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LIAS: Changed rating: RED","entity_name":"LIAS","entity_type":"gene"},{"created":"2022-02-13T18:30:54.747508+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3353","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARS2 as ready","entity_name":"LARS2","entity_type":"gene"},{"created":"2022-02-13T18:30:54.738387+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3353","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lars2 has been classified as Green List (High Evidence).","entity_name":"LARS2","entity_type":"gene"},{"created":"2022-02-13T18:30:46.603785+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3353","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LARS2 as Green List (high evidence)","entity_name":"LARS2","entity_type":"gene"},{"created":"2022-02-13T18:30:46.591006+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3353","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lars2 has been classified as Green List (High Evidence).","entity_name":"LARS2","entity_type":"gene"},{"created":"2022-02-13T18:30:03.143714+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3352","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMB1 as ready","entity_name":"LAMB1","entity_type":"gene"},{"created":"2022-02-13T18:30:03.133878+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3352","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamb1 has been classified as Green List (High Evidence).","entity_name":"LAMB1","entity_type":"gene"},{"created":"2022-02-13T18:29:07.886601+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3352","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LAMB1 as Green List (high evidence)","entity_name":"LAMB1","entity_type":"gene"},{"created":"2022-02-13T18:29:07.874633+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3352","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamb1 has been classified as Green List (High Evidence).","entity_name":"LAMB1","entity_type":"gene"},{"created":"2022-02-13T18:28:30.354978+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3351","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KPTN as ready","entity_name":"KPTN","entity_type":"gene"},{"created":"2022-02-13T18:28:30.343825+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3351","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kptn has been classified as Amber List (Moderate Evidence).","entity_name":"KPTN","entity_type":"gene"},{"created":"2022-02-13T18:28:26.443233+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3351","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KPTN were changed from MACROCEPHALY, NEURODEVELOPMENTAL DELAY, AND SEIZURES to Mental retardation, autosomal recessive 41 (MIM#615637)","entity_name":"KPTN","entity_type":"gene"},{"created":"2022-02-13T18:28:10.040007+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3350","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KPTN were set to ","entity_name":"KPTN","entity_type":"gene"},{"created":"2022-02-13T18:27:55.704193+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3349","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: 15 patients (9 from Amish families) reported with macrocephaly and intellectual disability with hom or chet variants in KPTN (PMID: 32808430).; to: 15 patients (9 from Amish families) reported with macrocephaly and intellectual disability with hom or chet variants in KPTN (PMID: 32808430). Age of onset of macrocephaly uncertain.","entity_name":"KPTN","entity_type":"gene"},{"created":"2022-02-13T18:27:41.874300+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3349","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KPTN: Changed rating: AMBER","entity_name":"KPTN","entity_type":"gene"},{"created":"2022-02-13T18:26:42.022524+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3349","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KNL1 as ready","entity_name":"KNL1","entity_type":"gene"},{"created":"2022-02-13T18:26:42.012245+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3349","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: knl1 has been classified as Green List (High Evidence).","entity_name":"KNL1","entity_type":"gene"},{"created":"2022-02-13T18:26:37.673316+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3349","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KNL1 were set to 26626498; 26621532; 22983954","entity_name":"KNL1","entity_type":"gene"},{"created":"2022-02-13T18:26:11.598902+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3348","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KNL1 as Green List (high evidence)","entity_name":"KNL1","entity_type":"gene"},{"created":"2022-02-13T18:26:11.589998+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3348","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: knl1 has been classified as Green List (High Evidence).","entity_name":"KNL1","entity_type":"gene"},{"created":"2022-02-13T18:25:32.823460+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3347","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KMT2B as ready","entity_name":"KMT2B","entity_type":"gene"},{"created":"2022-02-13T18:25:32.811488+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3347","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kmt2b has been classified as Red List (Low Evidence).","entity_name":"KMT2B","entity_type":"gene"},{"created":"2022-02-13T18:25:25.820150+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3347","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KMT2B were changed from Complex early-onset dystonia to Dystonia 28, childhood-onset, MIM#617284","entity_name":"KMT2B","entity_type":"gene"},{"created":"2022-02-13T18:25:12.734777+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3346","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KMT2B was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KMT2B","entity_type":"gene"},{"created":"2022-02-13T18:25:02.799903+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3345","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KMT2B as Red List (low evidence)","entity_name":"KMT2B","entity_type":"gene"},{"created":"2022-02-13T18:25:02.787761+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3345","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kmt2b has been classified as Red List (Low Evidence).","entity_name":"KMT2B","entity_type":"gene"},{"created":"2022-02-13T18:24:50.153979+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3344","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: ID described as part of the phenotype in some patients.; to: Clinical presentation is typically post-natal.","entity_name":"KMT2B","entity_type":"gene"},{"created":"2022-02-13T18:24:37.227693+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3344","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KMT2B: Changed rating: RED","entity_name":"KMT2B","entity_type":"gene"},{"created":"2022-02-13T18:24:03.641940+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3344","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KLHL7 as ready","entity_name":"KLHL7","entity_type":"gene"},{"created":"2022-02-13T18:24:03.632420+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3344","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: klhl7 has been classified as Green List (High Evidence).","entity_name":"KLHL7","entity_type":"gene"},{"created":"2022-02-13T18:23:58.606294+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3344","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KLHL7 were set to ","entity_name":"KLHL7","entity_type":"gene"},{"created":"2022-02-13T18:23:46.828637+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3343","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KLHL7 as Green List (high evidence)","entity_name":"KLHL7","entity_type":"gene"},{"created":"2022-02-13T18:23:46.817377+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: klhl7 has been classified as Green List (High Evidence).","entity_name":"KLHL7","entity_type":"gene"},{"created":"2022-02-13T18:23:33.416394+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3342","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: IUGR and contractures.; to: IUGR and contractures. More than 10 families reported.","entity_name":"KLHL7","entity_type":"gene"},{"created":"2022-02-13T18:23:09.062867+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3342","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Overall IUGR rather than microcephaly, head sizes when reported appear to be in the -1-2SD range.; to: IUGR and contractures.","entity_name":"KLHL7","entity_type":"gene"},{"created":"2022-02-13T18:22:56.026754+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3342","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KLHL7: Changed rating: GREEN","entity_name":"KLHL7","entity_type":"gene"},{"created":"2022-02-13T18:21:56.210648+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3342","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF5C as ready","entity_name":"KIF5C","entity_type":"gene"},{"created":"2022-02-13T18:21:56.199700+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3342","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif5c has been classified as Green List (High Evidence).","entity_name":"KIF5C","entity_type":"gene"},{"created":"2022-02-13T18:21:50.988770+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3342","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF5C were set to ","entity_name":"KIF5C","entity_type":"gene"},{"created":"2022-02-13T18:21:40.075627+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3341","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF5C was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF5C","entity_type":"gene"},{"created":"2022-02-13T18:21:30.535477+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3340","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF5C as Green List (high evidence)","entity_name":"KIF5C","entity_type":"gene"},{"created":"2022-02-13T18:21:30.520717+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3340","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif5c has been classified as Green List (High Evidence).","entity_name":"KIF5C","entity_type":"gene"},{"created":"2022-02-13T18:20:56.513167+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3339","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF2A as ready","entity_name":"KIF2A","entity_type":"gene"},{"created":"2022-02-13T18:20:56.502327+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3339","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif2a has been classified as Green List (High Evidence).","entity_name":"KIF2A","entity_type":"gene"},{"created":"2022-02-13T18:20:52.640672+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3339","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF2A were set to ","entity_name":"KIF2A","entity_type":"gene"},{"created":"2022-02-13T18:20:40.807772+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3338","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF2A was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF2A","entity_type":"gene"},{"created":"2022-02-13T18:20:17.886785+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3337","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF2A as Green List (high evidence)","entity_name":"KIF2A","entity_type":"gene"},{"created":"2022-02-13T18:20:17.875286+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3337","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif2a has been classified as Green List (High Evidence).","entity_name":"KIF2A","entity_type":"gene"},{"created":"2022-02-13T18:19:53.105725+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3336","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF14 as ready","entity_name":"KIF14","entity_type":"gene"},{"created":"2022-02-13T18:19:53.096798+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3336","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif14 has been classified as Green List (High Evidence).","entity_name":"KIF14","entity_type":"gene"},{"created":"2022-02-13T18:19:49.069771+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3336","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF14 were set to 29343805; 24128419; 30388224; 28892560","entity_name":"KIF14","entity_type":"gene"}]}