{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1138","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1136","results":[{"created":"2021-11-08T20:24:45.504264+11:00","panel_name":"Periventricular Grey Matter Heterotopia","panel_id":19,"panel_version":"1.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HNRNPK as Green List (high evidence)","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:24:45.494504+11:00","panel_name":"Periventricular Grey Matter Heterotopia","panel_id":19,"panel_version":"1.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hnrnpk has been classified as Green List (High Evidence).","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:24:13.599492+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HNRNPK as ready","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:24:13.589957+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hnrnpk has been classified as Green List (High Evidence).","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:24:06.138779+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HNRNPK as Green List (high evidence)","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:24:06.128456+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hnrnpk has been classified as Green List (High Evidence).","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:23:34.932658+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HNRNPK as ready","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:23:34.921669+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hnrnpk has been classified as Green List (High Evidence).","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:23:30.467392+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HNRNPK as Green List (high evidence)","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:23:30.456746+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hnrnpk has been classified as Green List (High Evidence).","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2021-11-08T20:23:03.296059+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9652","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HES7 as ready","entity_name":"HES7","entity_type":"gene"},{"created":"2021-11-08T20:23:03.285877+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9652","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hes7 has been classified as Green List (High Evidence).","entity_name":"HES7","entity_type":"gene"},{"created":"2021-11-08T20:22:54.711573+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9652","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HES7 were changed from  to Spondylocostal dysostosis 4, autosomal recessive MIM#613686","entity_name":"HES7","entity_type":"gene"},{"created":"2021-11-08T20:22:32.208206+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9651","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HES7 were set to ","entity_name":"HES7","entity_type":"gene"},{"created":"2021-11-08T20:22:15.458206+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9650","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HES7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HES7","entity_type":"gene"},{"created":"2021-11-08T20:21:14.128603+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9649","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DIS3L2 as ready","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:21:14.115025+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9649","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dis3l2 has been classified as Green List (High Evidence).","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:21:06.685791+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9649","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DIS3L2 were changed from  to Perlman syndrome MIM# 267000","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:20:48.901945+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9648","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DIS3L2 were set to ","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:20:29.728551+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9647","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DIS3L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:20:12.931993+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9646","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DIS3L2: Rating: GREEN; Mode of pathogenicity: None; Publications: 22306653, 28328139, 29950491; Phenotypes: Perlman syndrome MIM# 267000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:18:56.697564+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.271","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DIS3L2 as ready","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:18:56.687951+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.271","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dis3l2 has been classified as Green List (High Evidence).","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:18:51.949125+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.271","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DIS3L2 were changed from PERLMAN SYNDROME to Perlman syndrome MIM# 267000","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:18:39.339044+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.270","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DIS3L2 were set to ","entity_name":"DIS3L2","entity_type":"gene"},{"created":"2021-11-08T20:17:52.511548+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.269","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DHODH as ready","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-11-08T20:17:52.501266+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.269","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dhodh has been classified as Green List (High Evidence).","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-11-08T20:17:48.649973+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.269","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHODH were changed from POSTAXIAL ACROFACIAL DYSOSTOSIS to Miller syndrome, MIM# 263750","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-11-08T20:17:15.718186+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.268","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DHODH were set to ","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-11-08T20:16:35.823174+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4262","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDX3X as ready","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:16:35.813698+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4262","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddx3x has been classified as Green List (High Evidence).","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:16:32.177439+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4262","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DDX3X were changed from  to Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:15:56.594250+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4261","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DDX3X were set to ","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:15:04.286830+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4260","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DDX3X was changed from X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:14:47.471151+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4260","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DDX3X was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:14:25.141977+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9646","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDX3X as ready","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:14:25.131405+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9646","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddx3x has been classified as Green List (High Evidence).","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:14:08.184486+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4259","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DDX3X: Rating: GREEN; Mode of pathogenicity: None; Publications: 30266093, 26235985, 25533962, 33528536, 30936465, 31274575, 30817323; Phenotypes: Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:14:00.570295+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9646","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DDX3X were changed from  to Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:13:41.720874+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9645","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DDX3X were set to ","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:13:22.533740+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9644","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DDX3X was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:12:53.634744+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9643","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DDX3X: Rating: GREEN; Mode of pathogenicity: None; Publications: 30266093, 26235985, 25533962, 33528536, 30936465, 31274575, 30817323; Phenotypes: Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:11:29.727519+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.267","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDX3X as ready","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:11:29.717417+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.267","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddx3x has been classified as Green List (High Evidence).","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:11:25.979173+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.267","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DDX3X were changed from Intellectual disability; INTELLECTUAL DIABILITY; Mental retardation, X-linked 102, 300958 to Intellectual developmental disorder, X-linked, syndrome, Snijders Blok type MIM# 300958","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:11:13.183270+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.266","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DDX3X were set to 30266093; 26235985; 25533962","entity_name":"DDX3X","entity_type":"gene"},{"created":"2021-11-08T20:08:03.191991+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.265","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATAD1 as ready","entity_name":"ATAD1","entity_type":"gene"},{"created":"2021-11-08T20:08:03.181472+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.265","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atad1 has been classified as Green List (High Evidence).","entity_name":"ATAD1","entity_type":"gene"},{"created":"2021-11-08T20:07:30.625667+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.265","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ATAD1 as Green List (high evidence)","entity_name":"ATAD1","entity_type":"gene"},{"created":"2021-11-08T20:07:30.614475+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.265","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atad1 has been classified as Green List (High Evidence).","entity_name":"ATAD1","entity_type":"gene"},{"created":"2021-11-08T20:07:14.523557+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ATAD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hyperekplexia 4 - #618011; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ATAD1","entity_type":"gene"},{"created":"2021-11-08T20:05:22.526332+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: HSPD1: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HSPD1","entity_type":"gene"},{"created":"2021-11-08T20:05:13.580689+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSPD1 as ready","entity_name":"HSPD1","entity_type":"gene"},{"created":"2021-11-08T20:05:13.571144+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hspd1 has been classified as Green List (High Evidence).","entity_name":"HSPD1","entity_type":"gene"},{"created":"2021-11-08T20:05:09.543849+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.264","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSPD1 were changed from LEUKODYSTROPHY HYPOMYELINATING TYPE 4 to Leukodystrophy, hypomyelinating, 4, MIM# 612233","entity_name":"HSPD1","entity_type":"gene"},{"created":"2021-11-08T20:04:57.528508+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.263","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSPD1 were set to ","entity_name":"HSPD1","entity_type":"gene"},{"created":"2021-11-08T20:04:45.237181+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.262","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSPD1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HSPD1","entity_type":"gene"},{"created":"2021-11-08T20:04:21.137784+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.261","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSPD1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"HSPD1","entity_type":"gene"},{"created":"2021-11-08T20:04:07.137634+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.260","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HSPD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"HSPD1","entity_type":"gene"},{"created":"2021-11-08T20:02:45.193940+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.260","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADCY6 were changed from Lethal congenital contracture syndrome 8, MIM#616287 to Lethal congenital contracture syndrome 8, MIM#616287; MONDO:0014570","entity_name":"ADCY6","entity_type":"gene"},{"created":"2021-11-08T20:01:54.179023+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.259","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADCY6 as ready","entity_name":"ADCY6","entity_type":"gene"},{"created":"2021-11-08T20:01:54.165064+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.259","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy6 has been classified as Green List (High Evidence).","entity_name":"ADCY6","entity_type":"gene"},{"created":"2021-11-08T20:01:50.599275+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.259","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADCY6 were changed from Lethal congenital contracture syndrome 8 - #616287 to Lethal congenital contracture syndrome 8, MIM#616287","entity_name":"ADCY6","entity_type":"gene"},{"created":"2021-11-08T20:01:35.770528+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.258","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ADCY6 were set to 24319099, 26257172, 31846058; 33820833","entity_name":"ADCY6","entity_type":"gene"},{"created":"2021-11-08T20:01:21.351187+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.257","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADCY6 as Green List (high evidence)","entity_name":"ADCY6","entity_type":"gene"},{"created":"2021-11-08T20:01:21.341918+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.257","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy6 has been classified as Green List (High Evidence).","entity_name":"ADCY6","entity_type":"gene"},{"created":"2021-11-08T20:00:24.512252+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.256","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SIK3 as ready","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T20:00:24.499214+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.256","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sik3 has been classified as Amber List (Moderate Evidence).","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T20:00:14.413908+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.256","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SIK3 as Amber List (moderate evidence)","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T20:00:14.402148+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.256","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sik3 has been classified as Amber List (Moderate Evidence).","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:59:55.781614+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.255","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SIK3: Rating: AMBER; Mode of pathogenicity: None; Publications: 30232230, 22318228; Phenotypes: Spondyloepimetaphyseal dysplasia, Krakow type - #618162; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:58:52.176992+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9643","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SIK3 as ready","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:58:52.166263+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9643","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sik3 has been classified as Amber List (Moderate Evidence).","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:58:44.202462+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9643","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SIK3 were changed from ?Spondyloepimetaphyseal dysplasia, Krakow type - #618162 to Spondyloepimetaphyseal dysplasia, Krakow type - #618162","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:58:22.755541+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9642","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SIK3 as Amber List (moderate evidence)","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:58:22.745515+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9642","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sik3 has been classified as Amber List (Moderate Evidence).","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:57:55.130018+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SIK3 as ready","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:57:55.118697+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sik3 has been classified as Amber List (Moderate Evidence).","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:57:52.134906+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SIK3 were changed from ?Spondyloepimetaphyseal dysplasia, Krakow type - #618162 to Spondyloepimetaphyseal dysplasia, Krakow type - #618162","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:57:25.952858+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SIK3 as Amber List (moderate evidence)","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:57:25.943321+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sik3 has been classified as Amber List (Moderate Evidence).","entity_name":"SIK3","entity_type":"gene"},{"created":"2021-11-08T19:56:24.791449+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.255","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIPA as ready","entity_name":"LIPA","entity_type":"gene"},{"created":"2021-11-08T19:56:24.780744+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.255","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lipa has been classified as Green List (High Evidence).","entity_name":"LIPA","entity_type":"gene"},{"created":"2021-11-08T19:56:20.108432+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.255","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIPA were set to 12666227","entity_name":"LIPA","entity_type":"gene"},{"created":"2021-11-08T19:56:00.682773+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.254","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LIPA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Wolman disease, MIM# 278000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LIPA","entity_type":"gene"},{"created":"2021-11-08T19:01:06.913270+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.254","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCHS1 as ready","entity_name":"DCHS1","entity_type":"gene"},{"created":"2021-11-08T19:01:06.902198+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.254","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dchs1 has been classified as Green List (High Evidence).","entity_name":"DCHS1","entity_type":"gene"},{"created":"2021-11-08T19:01:02.457232+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.254","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DCHS1 were changed from PERIVENTRICULAR NEURONAL HETEROTOPIA to Van Maldergem syndrome 1, MIM# 601390","entity_name":"DCHS1","entity_type":"gene"},{"created":"2021-11-08T19:00:49.550592+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.253","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DCHS1 were set to ","entity_name":"DCHS1","entity_type":"gene"},{"created":"2021-11-08T18:59:34.507885+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.252","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSF4 as ready","entity_name":"HSF4","entity_type":"gene"},{"created":"2021-11-08T18:59:34.497627+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.252","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsf4 has been classified as Amber List (Moderate Evidence).","entity_name":"HSF4","entity_type":"gene"},{"created":"2021-11-08T18:59:31.207087+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.252","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSF4 were changed from CATARACT ZONULAR HSF4-RELATED; CATARACT MARNER TYPE to Cataract 5, multiple types MIM#116800","entity_name":"HSF4","entity_type":"gene"},{"created":"2021-11-08T18:59:14.890852+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.251","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSF4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HSF4","entity_type":"gene"},{"created":"2021-11-08T18:59:01.001736+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.250","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HSF4 as Amber List (moderate evidence)","entity_name":"HSF4","entity_type":"gene"},{"created":"2021-11-08T18:59:00.991603+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.250","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsf4 has been classified as Amber List (Moderate Evidence).","entity_name":"HSF4","entity_type":"gene"},{"created":"2021-11-08T18:57:46.171778+11:00","panel_name":"Differences of Sex Development","panel_id":99,"panel_version":"0.223","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSD17B3 as ready","entity_name":"HSD17B3","entity_type":"gene"},{"created":"2021-11-08T18:57:46.161739+11:00","panel_name":"Differences of Sex Development","panel_id":99,"panel_version":"0.223","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsd17b3 has been classified as Green List (High Evidence).","entity_name":"HSD17B3","entity_type":"gene"},{"created":"2021-11-08T18:57:43.396398+11:00","panel_name":"Differences of Sex Development","panel_id":99,"panel_version":"0.223","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSD17B3 were changed from  to Pseudohermaphroditism, male, with gynecomastia MIM#264300","entity_name":"HSD17B3","entity_type":"gene"},{"created":"2021-11-08T18:57:18.840488+11:00","panel_name":"Differences of Sex Development","panel_id":99,"panel_version":"0.222","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSD17B3 were set to ","entity_name":"HSD17B3","entity_type":"gene"},{"created":"2021-11-08T18:56:43.913327+11:00","panel_name":"Differences of Sex Development","panel_id":99,"panel_version":"0.221","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSD17B3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HSD17B3","entity_type":"gene"}]}