{"count":220212,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=880","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=878","results":[{"created":"2022-04-19T10:23:58.448520+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13036","user_name":"Ain Roesley","item_type":"entity","text":"Classified gene: CDKN2A as Red List (low evidence)","entity_name":"CDKN2A","entity_type":"gene"},{"created":"2022-04-19T10:23:58.407692+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13036","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdkn2a has been classified as Red List (Low Evidence).","entity_name":"CDKN2A","entity_type":"gene"},{"created":"2022-04-19T10:23:36.764401+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13035","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CDKN2A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Melanoma and neural system tumor syndrome} MIM#155755, {Melanoma, cutaneous malignant, 2} MIM#155601, {Melanoma-pancreatic cancer syndrome} MIM#606719; Mode of inheritance: None; Current diagnostic: yes","entity_name":"CDKN2A","entity_type":"gene"},{"created":"2022-04-19T10:09:09.926175+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13035","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CDKN1B were changed from  to Multiple endocrine neoplasia type 4, MEN4, OMIM #610755","entity_name":"CDKN1B","entity_type":"gene"},{"created":"2022-04-19T10:08:58.444272+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13034","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CDKN1B were set to ","entity_name":"CDKN1B","entity_type":"gene"},{"created":"2022-04-19T10:08:49.525801+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13034","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CDKN1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CDKN1B","entity_type":"gene"},{"created":"2022-04-19T10:08:26.848480+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13033","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CDKN1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 24819502, 17030811, 23555276; Phenotypes: Multiple endocrine neoplasia type 4, MEN4, OMIM #610755; Mode of inheritance: None; Current diagnostic: yes","entity_name":"CDKN1B","entity_type":"gene"},{"created":"2022-04-19T10:05:55.574311+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13033","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CDK4 as ready","entity_name":"CDK4","entity_type":"gene"},{"created":"2022-04-19T10:05:55.559699+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13033","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdk4 has been classified as Red List (Low Evidence).","entity_name":"CDK4","entity_type":"gene"},{"created":"2022-04-19T10:05:49.803265+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13033","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CDK4 were changed from  to {Melanoma, cutaneous malignant, 3} MIM#609048","entity_name":"CDK4","entity_type":"gene"},{"created":"2022-04-19T10:05:36.660067+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13032","user_name":"Ain Roesley","item_type":"entity","text":"Classified gene: CDK4 as Red List (low evidence)","entity_name":"CDK4","entity_type":"gene"},{"created":"2022-04-19T10:05:36.645789+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13032","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdk4 has been classified as Red List (Low Evidence).","entity_name":"CDK4","entity_type":"gene"},{"created":"2022-04-19T10:05:20.115249+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13031","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CDK4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Melanoma, cutaneous malignant, 3} MIM#609048; Mode of inheritance: None; Current diagnostic: yes","entity_name":"CDK4","entity_type":"gene"},{"created":"2022-04-19T09:52:48.465140+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.266","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CDK10 as ready","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:52:48.447224+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.266","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdk10 has been classified as Amber List (Moderate Evidence).","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:52:45.589411+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.266","user_name":"Ain Roesley","item_type":"entity","text":"Classified gene: CDK10 as Amber List (moderate evidence)","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:52:45.578377+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.266","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdk10 has been classified as Amber List (Moderate Evidence).","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:52:18.440044+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.265","user_name":"Ain Roesley","item_type":"entity","text":"gene: CDK10 was added\ngene: CDK10 was added to Hydrops fetalis. Sources: Literature\nMode of inheritance for gene: CDK10 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CDK10 were set to 28886341; 34974531\nPhenotypes for gene: CDK10 were set to Al Kaissi syndrome MIM#617694\nReview for gene: CDK10 was set to AMBER\ngene: CDK10 was marked as current diagnostic\nAdded comment: 1 out of 6 families reported hydrops \nSources: Literature","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:51:16.116701+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13031","user_name":"Ain Roesley","item_type":"entity","text":"changed review comment from: >5 families; to: 6 families thus far","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:50:27.624349+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.20","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CDK10 as ready","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:50:27.612131+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.20","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdk10 has been classified as Green List (High Evidence).","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:50:24.236571+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.20","user_name":"Ain Roesley","item_type":"entity","text":"Classified gene: CDK10 as Green List (high evidence)","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:50:24.227132+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.20","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdk10 has been classified as Green List (High Evidence).","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:50:13.045689+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.19","user_name":"Ain Roesley","item_type":"entity","text":"gene: CDK10 was added\ngene: CDK10 was added to Fetal anomalies. Sources: Literature\nMode of inheritance for gene: CDK10 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CDK10 were set to 28886341; 34974531\nPhenotypes for gene: CDK10 were set to Al Kaissi syndrome MIM#617694\nReview for gene: CDK10 was set to GREEN\ngene: CDK10 was marked as current diagnostic\nAdded comment: 6 families reported\r\n\r\n 1x with IUGR, 1x hydrocephalus and 1x with fetal hydrops, hydrocephalus, multicystic, dysplastic kidneys, lung hypoplasia, cardiomyopathy, retrognathia\r\n\r\nSmall birth weight/sizes reported in all \nSources: Literature","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:46:13.303941+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13031","user_name":"Ain Roesley","item_type":"entity","text":"Tag SV/CNV tag was added to gene: CDHR1.","entity_name":"CDHR1","entity_type":"gene"},{"created":"2022-04-19T09:40:22.269883+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13031","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CDK10 as ready","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:40:22.257938+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13031","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdk10 has been classified as Green List (High Evidence).","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:40:08.595097+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13031","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CDK10 were changed from  to Al Kaissi syndrome MIM#617694","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:40:08.180211+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13031","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CDK10 were set to ","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:39:51.083897+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13031","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CDK10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:39:27.123149+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13030","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CDK10: Rating: GREEN; Mode of pathogenicity: None; Publications: 28886341, 34974531; Phenotypes: Al Kaissi syndrome MIM#617694; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"CDK10","entity_type":"gene"},{"created":"2022-04-19T09:25:43.077365+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13030","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CDHR1 as ready","entity_name":"CDHR1","entity_type":"gene"},{"created":"2022-04-19T09:25:43.068451+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13030","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdhr1 has been classified as Green List (High Evidence).","entity_name":"CDHR1","entity_type":"gene"},{"created":"2022-04-19T09:25:36.474583+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13030","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CDHR1 were changed from  to Cone-rod dystrophy 15 MIM#613660; Retinitis pigmentosa 65 MIM#613660","entity_name":"CDHR1","entity_type":"gene"},{"created":"2022-04-19T09:25:25.632424+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13029","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CDHR1 were set to ","entity_name":"CDHR1","entity_type":"gene"},{"created":"2022-04-19T09:25:18.914843+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13029","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CDHR1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CDHR1","entity_type":"gene"},{"created":"2022-04-19T09:25:01.437899+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13028","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CDHR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20805371, 20087419, 34926197, 32277948, 32783370, 31387115, 32681094; Phenotypes: Cone-rod dystrophy 15 MIM#613660, Retinitis pigmentosa 65 MIM#613660; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"CDHR1","entity_type":"gene"},{"created":"2022-04-19T09:06:07.825345+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13028","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CDC73 as ready","entity_name":"CDC73","entity_type":"gene"},{"created":"2022-04-19T09:06:07.810211+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13028","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdc73 has been classified as Green List (High Evidence).","entity_name":"CDC73","entity_type":"gene"},{"created":"2022-04-19T09:05:59.983802+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13028","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CDC73 were set to ","entity_name":"CDC73","entity_type":"gene"},{"created":"2022-04-19T09:05:56.855927+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13028","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CDC73 were changed from  to Hyperparathyroidism-jaw tumour syndrome, MIM# 145001; Hyperparathyroidism, familial primary, MIM# 145000","entity_name":"CDC73","entity_type":"gene"},{"created":"2022-04-19T09:05:53.974137+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13028","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CDC73 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CDC73","entity_type":"gene"},{"created":"2022-04-19T09:05:29.244896+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13027","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CDC73: Rating: GREEN; Mode of pathogenicity: None; Publications: 12434154; Phenotypes: Hyperparathyroidism-jaw tumour syndrome, MIM# 145001, Hyperparathyroidism, familial primary, MIM# 145000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes","entity_name":"CDC73","entity_type":"gene"},{"created":"2022-04-19T09:04:31.540361+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13027","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CDC42 were changed from Takenouchi-Kosaki syndrome, MIM#616737 to Takenouchi-Kosaki syndrome, MIM#616737","entity_name":"CDC42","entity_type":"gene"},{"created":"2022-04-19T09:04:20.540585+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13026","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CDC42 were set to 29394990; 31601675; 32303876; 32231661","entity_name":"CDC42","entity_type":"gene"},{"created":"2022-04-19T09:04:10.652267+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13026","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CDC42 were changed from  to Takenouchi-Kosaki syndrome, MIM#616737","entity_name":"CDC42","entity_type":"gene"},{"created":"2022-04-19T09:03:57.883283+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13025","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CDC42 were set to ","entity_name":"CDC42","entity_type":"gene"},{"created":"2022-04-19T09:03:53.322530+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13025","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CDC42 as ready","entity_name":"CDC42","entity_type":"gene"},{"created":"2022-04-19T09:03:53.309192+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13025","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdc42 has been classified as Green List (High Evidence).","entity_name":"CDC42","entity_type":"gene"},{"created":"2022-04-19T09:03:46.989722+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13025","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CDC42 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CDC42","entity_type":"gene"},{"created":"2022-04-19T09:03:23.619945+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13024","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CDC42: Rating: GREEN; Mode of pathogenicity: None; Publications: 29394990, 31601675, 32303876, 32231661; Phenotypes: Takenouchi-Kosaki syndrome, MIM#616737; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes","entity_name":"CDC42","entity_type":"gene"},{"created":"2022-04-19T09:02:17.562933+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13024","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CDC14A as ready","entity_name":"CDC14A","entity_type":"gene"},{"created":"2022-04-19T09:02:17.552727+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13024","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cdc14a has been classified as Green List (High Evidence).","entity_name":"CDC14A","entity_type":"gene"},{"created":"2022-04-19T09:02:10.170404+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13024","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CDC14A were changed from  to Deafness, autosomal recessive 32, with or without immotile sperm, MIM# 608653","entity_name":"CDC14A","entity_type":"gene"},{"created":"2022-04-19T09:02:03.617738+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13023","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CDC14A were set to ","entity_name":"CDC14A","entity_type":"gene"},{"created":"2022-04-19T09:01:59.622563+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13023","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CDC14A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CDC14A","entity_type":"gene"},{"created":"2022-04-19T09:01:43.561463+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13022","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CDC14A: Rating: GREEN; Mode of pathogenicity: None; Publications: 29293958, 2725905; Phenotypes: Deafness, autosomal recessive 32, with or without immotile sperm, MIM# 608653; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"CDC14A","entity_type":"gene"},{"created":"2022-04-19T08:06:50.083838+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13022","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CD79B as ready","entity_name":"CD79B","entity_type":"gene"},{"created":"2022-04-19T08:06:50.074213+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13022","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cd79b has been classified as Green List (High Evidence).","entity_name":"CD79B","entity_type":"gene"},{"created":"2022-04-19T08:06:40.466544+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13022","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CD79B were changed from  to Agammaglobulinemia 6 MIM#612692","entity_name":"CD79B","entity_type":"gene"},{"created":"2022-04-19T08:06:29.573694+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13022","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CD79B were set to ","entity_name":"CD79B","entity_type":"gene"},{"created":"2022-04-19T08:06:18.003370+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13021","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CD79B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CD79B","entity_type":"gene"},{"created":"2022-04-19T08:05:50.296964+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13020","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CD79B: Rating: GREEN; Mode of pathogenicity: None; Publications: 17709424, 17675462, 33733381, 24722855; Phenotypes: Agammaglobulinemia 6 MIM#612692; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"CD79B","entity_type":"gene"},{"created":"2022-04-18T19:38:26.584962+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13020","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRDM5 as ready","entity_name":"PRDM5","entity_type":"gene"},{"created":"2022-04-18T19:38:26.576012+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13020","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prdm5 has been classified as Green List (High Evidence).","entity_name":"PRDM5","entity_type":"gene"},{"created":"2022-04-18T19:38:15.828760+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13020","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRDM5 were changed from  to Brittle cornea syndrome 2, MIM# 614170","entity_name":"PRDM5","entity_type":"gene"},{"created":"2022-04-18T19:37:52.974285+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13019","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRDM5 were set to ","entity_name":"PRDM5","entity_type":"gene"},{"created":"2022-04-18T19:37:30.505901+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13018","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRDM5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRDM5","entity_type":"gene"},{"created":"2022-04-18T19:37:08.758998+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13017","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRDM5: Rating: GREEN; Mode of pathogenicity: None; Publications: 21664999, 22122778, 21664999, 33739556, 27032025; Phenotypes: Brittle cornea syndrome 2, MIM# 614170; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRDM5","entity_type":"gene"},{"created":"2022-04-18T19:33:28.007678+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13017","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PREPL as ready","entity_name":"PREPL","entity_type":"gene"},{"created":"2022-04-18T19:33:27.995469+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13017","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prepl has been classified as Green List (High Evidence).","entity_name":"PREPL","entity_type":"gene"},{"created":"2022-04-18T19:33:10.527349+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13017","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PREPL were changed from  to Myasthenic syndrome, congenital, 22 MIM#616224; hypotonia-cystinuria syndrome; Disorders of amino acid transport","entity_name":"PREPL","entity_type":"gene"},{"created":"2022-04-18T19:28:27.077637+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13016","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PREPL were set to ","entity_name":"PREPL","entity_type":"gene"},{"created":"2022-04-18T19:27:57.189845+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13015","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PREPL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PREPL","entity_type":"gene"},{"created":"2022-04-18T19:26:54.562470+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.337","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRG4 as ready","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:26:54.549969+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.337","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prg4 has been classified as Green List (High Evidence).","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:24:44.536274+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.337","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRG4 were changed from  to Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, MIM# 208250","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:24:15.790938+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.336","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRG4 were set to ","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:23:46.017115+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.335","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRG4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:23:13.600443+10:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.334","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRG4: Rating: GREEN; Mode of pathogenicity: None; Publications: 10545950, 29397575; Phenotypes: Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, MIM# 208250; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:22:22.075941+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13014","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRG4 as ready","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:22:22.063652+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13014","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prg4 has been classified as Green List (High Evidence).","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:22:09.518287+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13014","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRG4 were changed from  to Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, MIM# 208250","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:21:49.140755+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13013","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRG4 were set to ","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:21:26.285048+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13012","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRG4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:21:04.729652+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13011","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRG4: Rating: GREEN; Mode of pathogenicity: None; Publications: 10545950, 29397575; Phenotypes: Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, MIM# 208250; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRG4","entity_type":"gene"},{"created":"2022-04-18T19:18:59.399835+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13011","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRICKLE2 were changed from Neurodevelopmental disorder, global developmental delay, behavioural difficulties ± epilepsy, autistic features, and attention deficit hyperactive disorder. to Neurodevelopmental disorder, MONDO:0700092; global developmental delay, behavioural difficulties ± epilepsy, autistic features, and attention deficit hyperactive disorder.","entity_name":"PRICKLE2","entity_type":"gene"},{"created":"2022-04-18T19:16:57.597911+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13010","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRICKLE1 as ready","entity_name":"PRICKLE1","entity_type":"gene"},{"created":"2022-04-18T19:16:57.583150+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13010","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prickle1 has been classified as Green List (High Evidence).","entity_name":"PRICKLE1","entity_type":"gene"},{"created":"2022-04-18T19:16:46.120793+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13010","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRICKLE1 were changed from  to Epilepsy, progressive myoclonic 1B, MIM# 612437","entity_name":"PRICKLE1","entity_type":"gene"},{"created":"2022-04-18T19:16:25.566385+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13009","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRICKLE1 were set to ","entity_name":"PRICKLE1","entity_type":"gene"},{"created":"2022-04-18T19:16:03.495085+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13008","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRICKLE1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PRICKLE1","entity_type":"gene"},{"created":"2022-04-18T19:15:42.789015+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13007","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRICKLE1: Rating: GREEN; Mode of pathogenicity: None; Publications: 34597683, 30564977, 30345727, 29790814, 26727662, 31035234; Phenotypes: Epilepsy, progressive myoclonic 1B, MIM# 612437; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PRICKLE1","entity_type":"gene"},{"created":"2022-04-18T19:07:58.257782+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13007","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKAR1A as ready","entity_name":"PRKAR1A","entity_type":"gene"},{"created":"2022-04-18T19:07:58.248383+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13007","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkar1a has been classified as Green List (High Evidence).","entity_name":"PRKAR1A","entity_type":"gene"},{"created":"2022-04-18T19:07:48.204295+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13007","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRKAR1A were changed from  to Acrodysostosis 1, with or without hormone resistance, MIM# 101800; Carney complex, type 1, MIM# 160980; Myxoma, intracardiac, MIM# 255960; Pigmented nodular adrenocortical disease, primary, 1, MIM# 610489","entity_name":"PRKAR1A","entity_type":"gene"},{"created":"2022-04-18T19:07:28.297625+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13006","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRKAR1A were set to ","entity_name":"PRKAR1A","entity_type":"gene"},{"created":"2022-04-18T19:07:05.759598+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13005","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRKAR1A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKAR1A","entity_type":"gene"},{"created":"2022-04-18T19:06:45.013046+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13004","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRKAR1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 10973256, 11115848, 12424709, 21651393; Phenotypes: Acrodysostosis 1, with or without hormone resistance, MIM# 101800, Carney complex, type 1, MIM# 160980, Myxoma, intracardiac, MIM# 255960, Pigmented nodular adrenocortical disease, primary, 1, MIM# 610489; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKAR1A","entity_type":"gene"},{"created":"2022-04-18T11:25:38.212498+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13004","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKCG as ready","entity_name":"PRKCG","entity_type":"gene"}]}