{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=598","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=596","results":[{"created":"2023-05-31T11:39:17.693160+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2155","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: samhd1 has been classified as Amber List (Moderate Evidence).","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2023-05-31T11:39:00.328527+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2154","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SAMHD1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Aicardi-Goutieres syndrome 5, MIM# 612952; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2023-05-31T11:37:43.459578+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2154","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review was removed from gene: CYP27A1.\nTag metabolic tag was added to gene: CYP27A1.","entity_name":"CYP27A1","entity_type":"gene"},{"created":"2023-05-31T11:37:32.299983+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2154","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CYP27A1 as Green List (high evidence)","entity_name":"CYP27A1","entity_type":"gene"},{"created":"2023-05-31T11:37:32.265306+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2154","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp27a1 has been classified as Green List (High Evidence).","entity_name":"CYP27A1","entity_type":"gene"},{"created":"2023-05-31T11:37:01.923706+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2153","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: CYP27A1: Added comment: Average age of onset is in late childhood, but a proportion would have onset < 5yo and early treatment beneficial.; Changed rating: GREEN; Changed publications: 24442603","entity_name":"CYP27A1","entity_type":"gene"},{"created":"2023-05-31T11:31:30.405140+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2153","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SGSH were set to ","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T11:31:19.252492+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2152","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SGSH as Amber List (moderate evidence)","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T11:31:19.227417+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2152","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgsh has been classified as Amber List (Moderate Evidence).","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T11:31:19.144794+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2152","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SGSH as Amber List (moderate evidence)","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T11:31:19.135544+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2152","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgsh has been classified as Amber List (Moderate Evidence).","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T11:31:18.064393+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2152","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SGSH as Amber List (moderate evidence)","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T11:31:18.052617+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2152","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgsh has been classified as Amber List (Moderate Evidence).","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T11:31:06.369041+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2151","user_name":"Zornitza Stark","item_type":"entity","text":"Tag clinical trial tag was added to gene: SGSH.","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T11:30:57.034720+10:00","panel_name":"Baby Screen+ newborn screening","panel_id":3931,"panel_version":"0.2151","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SGSH: Rating: AMBER; Mode of pathogenicity: None; Publications: 31044143; Phenotypes: Mucopolysaccharidosis type IIIA (Sanfilippo A), MIM# 252900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-05-31T10:58:51.490036+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.895","user_name":"Suliman Khan","item_type":"entity","text":"reviewed gene: MCM6: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 37198333; Phenotypes: Neurodevelopmental disorder, MONDO:0700092, MCM6-related; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MCM6","entity_type":"gene"},{"created":"2023-05-30T18:51:33.598993+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ANG as ready","entity_name":"ANG","entity_type":"gene"},{"created":"2023-05-30T18:51:33.587373+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ang has been classified as Green List (High Evidence).","entity_name":"ANG","entity_type":"gene"},{"created":"2023-05-30T18:51:28.633464+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ANG were changed from  to Amyotrophic Lateral Sclerosis 9 (MONDO: 0012753; MIM#611895)","entity_name":"ANG","entity_type":"gene"},{"created":"2023-05-30T18:50:55.453678+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ANG were set to ","entity_name":"ANG","entity_type":"gene"},{"created":"2023-05-30T18:50:19.809013+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ANG was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ANG","entity_type":"gene"},{"created":"2023-05-30T18:49:40.365952+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALS2 as ready","entity_name":"ALS2","entity_type":"gene"},{"created":"2023-05-30T18:49:40.357853+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: als2 has been classified as Green List (High Evidence).","entity_name":"ALS2","entity_type":"gene"},{"created":"2023-05-30T18:49:36.789129+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALS2 were changed from  to Amyotrophic lateral sclerosis 2, juvenile (MIM# 205100; MONDO: MONDO:0008780)","entity_name":"ALS2","entity_type":"gene"},{"created":"2023-05-30T18:49:03.835894+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALS2 were set to ","entity_name":"ALS2","entity_type":"gene"},{"created":"2023-05-30T18:48:27.153806+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALS2","entity_type":"gene"},{"created":"2023-05-30T18:47:41.132721+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ASCC1 as ready","entity_name":"ASCC1","entity_type":"gene"},{"created":"2023-05-30T18:47:41.120678+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ascc1 has been classified as Green List (High Evidence).","entity_name":"ASCC1","entity_type":"gene"},{"created":"2023-05-30T18:47:38.731352+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ASCC1 were changed from  to spinal muscular atrophy with congenital bone fractures 2 (MONDO:0014807; MIM#616867)","entity_name":"ASCC1","entity_type":"gene"},{"created":"2023-05-30T18:47:03.234586+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ASCC1 were set to ","entity_name":"ASCC1","entity_type":"gene"},{"created":"2023-05-30T18:46:29.499449+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ASCC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ASCC1","entity_type":"gene"},{"created":"2023-05-30T18:44:10.080701+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: APTX as ready","entity_name":"APTX","entity_type":"gene"},{"created":"2023-05-30T18:44:10.049517+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aptx has been classified as Green List (High Evidence).","entity_name":"APTX","entity_type":"gene"},{"created":"2023-05-30T18:44:07.562422+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: APTX were changed from Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia; Hereditary Neuropathies to Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (MIM#208920)","entity_name":"APTX","entity_type":"gene"},{"created":"2023-05-30T18:43:47.628135+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: APTX were set to ","entity_name":"APTX","entity_type":"gene"},{"created":"2023-05-30T18:42:28.693122+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B4GALNT1 as ready","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2023-05-30T18:42:28.681684+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4galnt1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2023-05-30T18:42:25.046774+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B4GALNT1 were changed from Spastic paraplegia, intellectual disability, ataxia, dystonia, axonal sensory-motor neuropathy to Spastic paraplegia 26, autosomal recessive (MIM#609195; MONDO:0012213)","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2023-05-30T18:42:06.937706+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GALNT1 were set to ","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2023-05-30T18:41:50.116036+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B4GALNT1 as Amber List (moderate evidence)","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2023-05-30T18:41:50.102261+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4galnt1 has been classified as Amber List (Moderate Evidence).","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2023-05-30T18:41:15.613959+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BAG3 as ready","entity_name":"BAG3","entity_type":"gene"},{"created":"2023-05-30T18:41:15.604284+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bag3 has been classified as Amber List (Moderate Evidence).","entity_name":"BAG3","entity_type":"gene"},{"created":"2023-05-30T18:41:13.137893+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BAG3 were changed from Myopathy, myofibrillar, 6 612954; Cardiomyopathy, dilated, 1HH, 613881; HMSN to Myopathy, myofibrillar, 6 (MIM#612954; MONDO:0013061)","entity_name":"BAG3","entity_type":"gene"},{"created":"2023-05-30T18:40:56.417779+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BAG3 were set to ","entity_name":"BAG3","entity_type":"gene"},{"created":"2023-05-30T18:40:41.624549+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BAG3 as Amber List (moderate evidence)","entity_name":"BAG3","entity_type":"gene"},{"created":"2023-05-30T18:40:41.613870+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bag3 has been classified as Amber List (Moderate Evidence).","entity_name":"BAG3","entity_type":"gene"},{"created":"2023-05-30T18:40:11.575932+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CNTNAP1 as ready","entity_name":"CNTNAP1","entity_type":"gene"},{"created":"2023-05-30T18:40:11.565816+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cntnap1 has been classified as Green List (High Evidence).","entity_name":"CNTNAP1","entity_type":"gene"},{"created":"2023-05-30T18:40:08.409314+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CNTNAP1 were changed from Hypomyelinating neuropathy, congenital, 3, 618186 to Hypomyelinating neuropathy, congenital, 3 (MONDO:0017049; MIM#618186)","entity_name":"CNTNAP1","entity_type":"gene"},{"created":"2023-05-30T18:39:51.828984+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CNTNAP1 were set to ","entity_name":"CNTNAP1","entity_type":"gene"},{"created":"2023-05-30T18:39:15.479844+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COX10 as ready","entity_name":"COX10","entity_type":"gene"},{"created":"2023-05-30T18:39:15.471734+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cox10 has been classified as Amber List (Moderate Evidence).","entity_name":"COX10","entity_type":"gene"},{"created":"2023-05-30T18:39:08.938845+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COX10 were changed from Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency; HMSN to Mitochondrial complex IV deficiency, nuclear type 3 (MIM#619046)","entity_name":"COX10","entity_type":"gene"},{"created":"2023-05-30T18:38:52.099768+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.155","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COX10 were set to ","entity_name":"COX10","entity_type":"gene"},{"created":"2023-05-30T18:38:35.717161+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COX10 as Amber List (moderate evidence)","entity_name":"COX10","entity_type":"gene"},{"created":"2023-05-30T18:38:35.702608+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cox10 has been classified as Amber List (Moderate Evidence).","entity_name":"COX10","entity_type":"gene"},{"created":"2023-05-30T18:38:03.900290+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTDP1 as ready","entity_name":"CTDP1","entity_type":"gene"},{"created":"2023-05-30T18:38:03.888049+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctdp1 has been classified as Green List (High Evidence).","entity_name":"CTDP1","entity_type":"gene"},{"created":"2023-05-30T18:38:01.338424+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTDP1 were changed from Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN); HMSN to Congenital cataracts, facial dysmorphism, and neuropathy (MIM#604168)","entity_name":"CTDP1","entity_type":"gene"},{"created":"2023-05-30T18:37:32.549127+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.152","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTDP1 were set to ","entity_name":"CTDP1","entity_type":"gene"},{"created":"2023-05-30T18:37:14.367395+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deep intronic tag was added to gene: CTDP1.\nTag founder tag was added to gene: CTDP1.","entity_name":"CTDP1","entity_type":"gene"},{"created":"2023-05-30T18:37:04.579975+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTDP1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital cataracts, facial dysmorphism, and neuropathy (MIM#604168); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTDP1","entity_type":"gene"},{"created":"2023-05-30T18:31:17.899813+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYP2U1 as ready","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2023-05-30T18:31:17.891859+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp2u1 has been classified as Green List (High Evidence).","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2023-05-30T18:31:15.018447+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CYP2U1 were changed from Onset first decade, spastic paraplegia, rarely dystonia and cognitive impairment, subclinical sensory-motor axonal neuropathy to Spastic paraplegia 56, autosomal recessive, MIM#615030","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2023-05-30T18:30:58.106732+10:00","panel_name":"Hereditary Neuropathy - complex","panel_id":3070,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CYP2U1 were set to ","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2023-05-30T18:30:13.834457+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.109","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RASA1 were set to 33461977","entity_name":"RASA1","entity_type":"gene"},{"created":"2023-05-30T18:29:56.420149+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.108","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RASA1: Added comment: PMID 36980822: 21 cases presenting with hydrops.; Changed publications: 33461977, 36980822","entity_name":"RASA1","entity_type":"gene"},{"created":"2023-05-30T18:28:58.552172+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RASA1 were set to 26096958","entity_name":"RASA1","entity_type":"gene"},{"created":"2023-05-30T18:21:03.672557+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RASA1 as Green List (high evidence)","entity_name":"RASA1","entity_type":"gene"},{"created":"2023-05-30T18:21:03.661138+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rasa1 has been classified as Green List (High Evidence).","entity_name":"RASA1","entity_type":"gene"},{"created":"2023-05-30T18:20:01.886819+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.86","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADCY5 as ready","entity_name":"ADCY5","entity_type":"gene"},{"created":"2023-05-30T18:20:01.872580+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy5 has been classified as Green List (High Evidence).","entity_name":"ADCY5","entity_type":"gene"},{"created":"2023-05-30T18:19:50.597787+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.86","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADCY5 as Green List (high evidence)","entity_name":"ADCY5","entity_type":"gene"},{"created":"2023-05-30T18:19:50.589786+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy5 has been classified as Green List (High Evidence).","entity_name":"ADCY5","entity_type":"gene"},{"created":"2023-05-30T18:19:04.731128+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.85","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACTB as ready","entity_name":"ACTB","entity_type":"gene"},{"created":"2023-05-30T18:19:04.719432+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.85","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actb has been classified as Green List (High Evidence).","entity_name":"ACTB","entity_type":"gene"},{"created":"2023-05-30T18:19:00.230769+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.85","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ACTB was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ACTB","entity_type":"gene"},{"created":"2023-05-30T18:18:26.737276+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.84","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACTB as Green List (high evidence)","entity_name":"ACTB","entity_type":"gene"},{"created":"2023-05-30T18:18:26.729437+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actb has been classified as Green List (High Evidence).","entity_name":"ACTB","entity_type":"gene"},{"created":"2023-05-30T18:17:48.605946+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACADM as ready","entity_name":"ACADM","entity_type":"gene"},{"created":"2023-05-30T18:17:48.595142+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acadm has been classified as Amber List (Moderate Evidence).","entity_name":"ACADM","entity_type":"gene"},{"created":"2023-05-30T18:17:26.607124+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACADM as Amber List (moderate evidence)","entity_name":"ACADM","entity_type":"gene"},{"created":"2023-05-30T18:17:26.599306+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acadm has been classified as Amber List (Moderate Evidence).","entity_name":"ACADM","entity_type":"gene"},{"created":"2023-05-30T18:16:34.447771+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.82","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADNP as ready","entity_name":"ADNP","entity_type":"gene"},{"created":"2023-05-30T18:16:34.436670+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.82","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adnp has been classified as Amber List (Moderate Evidence).","entity_name":"ADNP","entity_type":"gene"},{"created":"2023-05-30T18:16:30.638205+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.82","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADNP as Amber List (moderate evidence)","entity_name":"ADNP","entity_type":"gene"},{"created":"2023-05-30T18:16:30.628935+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.82","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adnp has been classified as Amber List (Moderate Evidence).","entity_name":"ADNP","entity_type":"gene"},{"created":"2023-05-30T18:15:44.644086+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.81","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AHDC1 as ready","entity_name":"AHDC1","entity_type":"gene"},{"created":"2023-05-30T18:15:44.636592+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.81","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ahdc1 has been classified as Green List (High Evidence).","entity_name":"AHDC1","entity_type":"gene"},{"created":"2023-05-30T18:15:40.355693+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.81","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AHDC1 as Green List (high evidence)","entity_name":"AHDC1","entity_type":"gene"},{"created":"2023-05-30T18:15:40.343891+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.81","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ahdc1 has been classified as Green List (High Evidence).","entity_name":"AHDC1","entity_type":"gene"},{"created":"2023-05-30T18:14:51.789953+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.80","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AKT3 as ready","entity_name":"AKT3","entity_type":"gene"},{"created":"2023-05-30T18:14:51.780944+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.80","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: akt3 has been classified as Red List (Low Evidence).","entity_name":"AKT3","entity_type":"gene"},{"created":"2023-05-30T18:14:49.084566+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.80","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AKT3 were changed from  to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM# 615937","entity_name":"AKT3","entity_type":"gene"},{"created":"2023-05-30T18:14:17.556173+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.79","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AKT3 as Red List (low evidence)","entity_name":"AKT3","entity_type":"gene"},{"created":"2023-05-30T18:14:17.545003+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.79","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: akt3 has been classified as Red List (Low Evidence).","entity_name":"AKT3","entity_type":"gene"},{"created":"2023-05-30T18:13:47.030745+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.78","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AKT3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM# 615937; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"AKT3","entity_type":"gene"},{"created":"2023-05-30T18:12:34.054166+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.78","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARG1 as ready","entity_name":"ARG1","entity_type":"gene"}]}