{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1812","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1810","results":[{"created":"2020-05-04T08:49:38.268969+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2706","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CCDC65: Rating: GREEN; Mode of pathogenicity: None; Publications: 23991085, 24094744; Phenotypes: Ciliary dyskinesia, primary, 27, MIM# 615504; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:48:25.841258+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CCDC65 as ready","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:48:25.831762+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc65 has been classified as Green List (High Evidence).","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:48:21.623901+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: CCDC65.","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:48:18.103395+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CCDC65 were changed from  to Ciliary dyskinesia, primary, 27, MIM# 615504","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:47:45.497596+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CCDC65 were set to ","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:47:14.958618+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CCDC65 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:46:39.619615+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CCDC65: Rating: GREEN; Mode of pathogenicity: None; Publications: 23991085, 24094744; Phenotypes: Ciliary dyskinesia, primary, 27, MIM# 615504; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:39:20.278950+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCDC65 as Green List (high evidence)","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:39:20.269391+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc65 has been classified as Green List (High Evidence).","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:38:47.858515+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CCDC65: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ciliary dyskinesia, primary, 27, MIM# 615504; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:37:43.990188+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their review","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:37:40.518712+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:34:18.911025+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.73","user_name":"Elena Savva","item_type":"entity","text":"gene: SCAPER was added\ngene: SCAPER was added to Ciliopathies. Sources: Expert Review\nMode of inheritance for gene: SCAPER was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SCAPER were set to PMID:30723319; 28794130; 31069901; 31192531; 30723319\nPhenotypes for gene: SCAPER were set to Intellectual developmental disorder and retinitis pigmentosa, OMIM #618195; Bardet-Biedl syndrome\nReview for gene: SCAPER was set to GREEN\nAdded comment: Two distantly related consanguineous families reported plus note some of the individuals in the preceding papers had a BBS phenotype. Functional data to associate SCAPER with ciliary dynamics and disassembly.\r\nSources: Literature \nSources: Expert Review","entity_name":"SCAPER","entity_type":"gene"},{"created":"2020-05-04T08:32:26.273827+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CCDC65 as ready","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:32:26.267456+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Agree, single founder variant reported, functional data.","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:32:26.222311+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc65 has been classified as Amber List (Moderate Evidence).","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:32:07.227686+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CCDC65 were changed from  to Ciliary dyskinesia, primary, 27, MIM# 615504","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:31:42.332342+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CCDC65 were set to ","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:31:15.818634+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CCDC65 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:29:59.661749+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCDC65 as Amber List (moderate evidence)","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:29:59.648608+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc65 has been classified as Amber List (Moderate Evidence).","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:28:59.915834+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: CCDC65.","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-04T08:14:52.229504+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.35","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: CCDC65: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 23991085, 24094744; Phenotypes: Ciliary dyskinesia, primary, 27 615504; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CCDC65","entity_type":"gene"},{"created":"2020-05-03T18:20:58.853389+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADAR as ready","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-05-03T18:20:58.844463+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adar has been classified as Green List (High Evidence).","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-05-03T18:20:52.526556+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADAR as Green List (high evidence)","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-05-03T18:20:52.514409+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adar has been classified as Green List (High Evidence).","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-05-03T18:20:43.358975+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ADAR was added\ngene: ADAR was added to Leukodystrophy - paediatric. Sources: Expert list\nMode of inheritance for gene: ADAR was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ADAR were set to Aicardi-Goutieres syndrome 6, MIM#\t615010\nReview for gene: ADAR was set to GREEN\nAdded comment: White matter changes reported in some. \nSources: Expert list","entity_name":"ADAR","entity_type":"gene"},{"created":"2020-05-03T18:14:56.778485+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYP7B1 as ready","entity_name":"CYP7B1","entity_type":"gene"},{"created":"2020-05-03T18:14:56.763886+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp7b1 has been classified as Green List (High Evidence).","entity_name":"CYP7B1","entity_type":"gene"},{"created":"2020-05-03T18:14:52.896892+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CYP7B1 as Green List (high evidence)","entity_name":"CYP7B1","entity_type":"gene"},{"created":"2020-05-03T18:14:52.883339+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp7b1 has been classified as Green List (High Evidence).","entity_name":"CYP7B1","entity_type":"gene"},{"created":"2020-05-03T18:14:41.564066+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CYP7B1 was added\ngene: CYP7B1 was added to Leukodystrophy - paediatric. Sources: Expert list\nMode of inheritance for gene: CYP7B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP7B1 were set to 24117163; 19439420; 19187859\nPhenotypes for gene: CYP7B1 were set to Spastic paraplegia 5A, autosomal recessive, MIM#\t270800\nReview for gene: CYP7B1 was set to GREEN\nAdded comment: White matter lesions have been reported as a feature of the condition in >3 cases. Age of onset highly variable, generally in adolescence but onset in early childhood reported. \nSources: Expert list","entity_name":"CYP7B1","entity_type":"gene"},{"created":"2020-05-03T18:11:14.378569+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPC1 as ready","entity_name":"NPC1","entity_type":"gene"},{"created":"2020-05-03T18:11:14.369549+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: npc1 has been classified as Green List (High Evidence).","entity_name":"NPC1","entity_type":"gene"},{"created":"2020-05-03T18:11:07.565088+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NPC1 as Green List (high evidence)","entity_name":"NPC1","entity_type":"gene"},{"created":"2020-05-03T18:11:07.543945+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: npc1 has been classified as Green List (High Evidence).","entity_name":"NPC1","entity_type":"gene"},{"created":"2020-05-03T18:10:58.731582+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NPC1 was added\ngene: NPC1 was added to Leukodystrophy - paediatric. Sources: Expert list\nMode of inheritance for gene: NPC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NPC1 were set to 26910362; 29406968\nPhenotypes for gene: NPC1 were set to Niemann-Pick disease, type C1/D, MIM#\t257220\nReview for gene: NPC1 was set to GREEN\nAdded comment: Age of onset/severity highly variable. \nSources: Expert list","entity_name":"NPC1","entity_type":"gene"},{"created":"2020-05-03T18:05:48.306652+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPIA as ready","entity_name":"RPIA","entity_type":"gene"},{"created":"2020-05-03T18:05:48.297460+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpia has been classified as Green List (High Evidence).","entity_name":"RPIA","entity_type":"gene"},{"created":"2020-05-03T18:05:42.344155+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RPIA as Green List (high evidence)","entity_name":"RPIA","entity_type":"gene"},{"created":"2020-05-03T18:05:42.335359+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpia has been classified as Green List (High Evidence).","entity_name":"RPIA","entity_type":"gene"},{"created":"2020-05-03T18:05:34.582801+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RPIA was added\ngene: RPIA was added to Leukodystrophy - paediatric. Sources: Expert list\nMode of inheritance for gene: RPIA was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RPIA were set to 31247379; 14988808; 31056085\nPhenotypes for gene: RPIA were set to Ribose 5-phosphate isomerase deficiency, MIM#\t608611\nReview for gene: RPIA was set to GREEN\nAdded comment: Four unrelated individuals described to date, variable onset of leukodystrophy in childhood/adolescence, though other symptoms generally precede. \nSources: Expert list","entity_name":"RPIA","entity_type":"gene"},{"created":"2020-05-03T18:02:32.178762+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SNORD118 as ready","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-05-03T18:02:32.156303+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snord118 has been classified as Green List (High Evidence).","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-05-03T18:02:28.427851+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SNORD118 as Green List (high evidence)","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-05-03T18:02:28.416048+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snord118 has been classified as Green List (High Evidence).","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-05-03T18:02:17.805253+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SNORD118: Changed rating: GREEN; Changed phenotypes: Leukoencephalopathy, brain calcifications, and cysts 614561","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-05-03T18:02:02.172811+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SNORD118 was added\ngene: SNORD118 was added to Leukodystrophy - paediatric. Sources: Expert list\nMode of inheritance for gene: SNORD118 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SNORD118 were set to 27571260\nPhenotypes for gene: SNORD118 were set to Leukoencephalopathy, brain calcifications, and cysts\t614561\nAdded comment: Over 30 families reported, age at presentation ranged between infancy and 54 years. \nSources: Expert list","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-05-03T17:44:31.616058+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCAF17 as ready","entity_name":"DCAF17","entity_type":"gene"},{"created":"2020-05-03T17:44:31.602847+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcaf17 has been classified as Green List (High Evidence).","entity_name":"DCAF17","entity_type":"gene"},{"created":"2020-05-03T17:44:26.033183+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DCAF17 as Green List (high evidence)","entity_name":"DCAF17","entity_type":"gene"},{"created":"2020-05-03T17:44:26.022071+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcaf17 has been classified as Green List (High Evidence).","entity_name":"DCAF17","entity_type":"gene"},{"created":"2020-05-03T17:43:55.629112+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DCAF17 was added\ngene: DCAF17 was added to Leukodystrophy - paediatric. Sources: Expert list\nMode of inheritance for gene: DCAF17 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DCAF17 were set to 19026396; 20507343\nPhenotypes for gene: DCAF17 were set to Woodhouse-Sakati syndrome, MIM#\t241080\nReview for gene: DCAF17 was set to GREEN\nAdded comment: White matter changes are part of the phenotype. \nSources: Expert list","entity_name":"DCAF17","entity_type":"gene"},{"created":"2020-05-03T17:42:22.493063+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTEN as ready","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-05-03T17:42:22.480321+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pten has been classified as Green List (High Evidence).","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-05-03T17:42:17.794456+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PTEN as Green List (high evidence)","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-05-03T17:42:17.785959+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pten has been classified as Green List (High Evidence).","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-05-03T17:42:08.845386+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PTEN was added\ngene: PTEN was added to Leukodystrophy - paediatric. Sources: Expert list\nMode of inheritance for gene: PTEN was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PTEN were set to 29720545; 29152901; 30664625\nPhenotypes for gene: PTEN were set to Cowden syndrome 1, MIM# 158350\nReview for gene: PTEN was set to GREEN\nAdded comment: White matter changes described in many individuals. \nSources: Expert list","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-05-03T13:59:03.067918+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2706","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C21orf59 as ready","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:59:03.056993+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2706","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c21orf59 has been classified as Green List (High Evidence).","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:58:50.649808+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2706","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C21orf59 were changed from  to Ciliary dyskinesia, primary, 26, MIM# 615500","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:58:18.634960+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2705","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C21orf59 were set to ","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:57:49.309719+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2704","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C21orf59 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:57:28.368987+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2703","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C21orf59.","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:57:13.351189+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2703","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C21orf59: Rating: GREEN; Mode of pathogenicity: None; Publications: 24094744; Phenotypes: Ciliary dyskinesia, primary, 26, MIM# 615500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:56:14.294067+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C21orf59 as ready","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:56:14.285150+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c21orf59 has been classified as Green List (High Evidence).","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:56:08.898119+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C21orf59 were changed from  to Ciliary dyskinesia, primary, 26, MIM# 615500","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:55:46.112887+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C21orf59 were set to ","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:55:19.400943+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C21orf59 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:54:52.439042+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C21orf59.","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:54:43.256073+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C21orf59: Rating: GREEN; Mode of pathogenicity: None; Publications: 24094744; Phenotypes: Ciliary dyskinesia, primary, 26, MIM# 615500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:53:53.119893+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: At least three unrelated families reported.; to: At least three unrelated families reported. HGNC approved name CFAP298.","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:53:31.433001+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C21orf59 as ready","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:53:31.424229+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c21orf59 has been classified as Green List (High Evidence).","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:53:28.524144+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C21orf59 were changed from  to Ciliary dyskinesia, primary, 26, MIM# 615500","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:53:04.902498+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C21orf59 were set to ","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:52:42.008730+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C21orf59 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:52:12.286995+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C21orf59: Rating: GREEN; Mode of pathogenicity: None; Publications: 24094744; Phenotypes: Ciliary dyskinesia, primary, 26, MIM# 615500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:51:21.540003+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C21orf59.","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-03T13:49:23.940954+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2703","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WISP3 as ready","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:49:23.927319+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2703","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wisp3 has been classified as Green List (High Evidence).","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:49:11.174544+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2703","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WISP3 were changed from  to Arthropathy, progressive pseudorheumatoid, of childhood, MIM# 208230; Spondyloepiphyseal dysplasia tarda with progressive arthropathy, MIM# 208230","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:48:47.140543+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2702","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WISP3 were set to ","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:48:25.504473+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2701","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WISP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:48:05.006236+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2700","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: WISP3.","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:47:50.940591+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2700","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WISP3: Rating: GREEN; Mode of pathogenicity: None; Publications: 10471507; Phenotypes: Arthropathy, progressive pseudorheumatoid, of childhood, MIM# 208230, Spondyloepiphyseal dysplasia tarda with progressive arthropathy, MIM# 208230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:45:50.631955+10:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WISP3 as ready","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:45:50.626371+10:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: HGNC approved name CCN6","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:45:50.585153+10:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wisp3 has been classified as Green List (High Evidence).","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:45:43.491684+10:00","panel_name":"Mackenzie's Mission_Reproductive Carrier Screening","panel_id":3139,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: WISP3.","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:45:17.056172+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WISP3 as ready","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:45:17.052282+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: HGNC approved name CCN6","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:45:17.021931+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wisp3 has been classified as Green List (High Evidence).","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:45:01.819864+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: WISP3.","entity_name":"WISP3","entity_type":"gene"},{"created":"2020-05-03T13:44:24.311183+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.445","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATP5E as ready","entity_name":"ATP5E","entity_type":"gene"},{"created":"2020-05-03T13:44:24.307280+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.445","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: HGNC approved name ATP5F1E.","entity_name":"ATP5E","entity_type":"gene"},{"created":"2020-05-03T13:44:24.277118+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.445","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp5e has been classified as Amber List (Moderate Evidence).","entity_name":"ATP5E","entity_type":"gene"}]}