{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=216","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=214","results":[{"created":"2025-05-31T11:29:07.972079+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.82","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: EDN3 as Green List (high evidence)","entity_name":"EDN3","entity_type":"gene"},{"created":"2025-05-31T11:29:07.965261+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.82","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: edn3 has been classified as Green List (High Evidence).","entity_name":"EDN3","entity_type":"gene"},{"created":"2025-05-31T11:23:53.516933+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.79","user_name":"Bryony Thompson","item_type":"entity","text":"gene: EDN3 was added\ngene: EDN3 was added to Hereditary Pigmentary Disorders. Sources: Expert list\nMode of inheritance for gene: EDN3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: EDN3 were set to 8630502; 11303518; 9359047; 10231870; 30171849; 27370713\nPhenotypes for gene: EDN3 were set to Waardenburg syndrome type 4B MONDO:0013201","entity_name":"EDN3","entity_type":"gene"},{"created":"2025-05-31T11:17:37.193503+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.78","user_name":"Bryony Thompson","item_type":"entity","text":"gene: EDNRB was added\ngene: EDNRB was added to Hereditary Pigmentary Disorders. Sources: Expert list\nMode of inheritance for gene: EDNRB was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal\nPublications for gene: EDNRB were set to 28502583; 25852447; 21373256; 16237557; 11773966; 11891690; 8001158; 10528251; 10528251; 19764031; 28236341\nPhenotypes for gene: EDNRB were set to Waardenburg syndrome type 4A MONDO:0010192","entity_name":"EDNRB","entity_type":"gene"},{"created":"2025-05-31T11:14:55.523813+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.77","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: PAX3 as ready","entity_name":"PAX3","entity_type":"gene"},{"created":"2025-05-31T11:14:55.514580+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.77","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: pax3 has been classified as Green List (High Evidence).","entity_name":"PAX3","entity_type":"gene"},{"created":"2025-05-31T11:14:47.780466+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.77","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: PAX3 as Green List (high evidence)","entity_name":"PAX3","entity_type":"gene"},{"created":"2025-05-31T11:14:47.766210+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.77","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: pax3 has been classified as Green List (High Evidence).","entity_name":"PAX3","entity_type":"gene"},{"created":"2025-05-31T11:14:38.655026+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.76","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PAX3 was added\ngene: PAX3 was added to Hereditary Pigmentary Disorders. Sources: Expert list\nMode of inheritance for gene: PAX3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PAX3 were set to 27759048; 7897628; 28690861; 30314436; 25932447\nPhenotypes for gene: PAX3 were set to Waardenburg syndrome MONDO:0018094\nReview for gene: PAX3 was set to GREEN\ngene: PAX3 was marked as current diagnostic\nAdded comment: Heterozygous loss-of-function variants in this gene cause Waardenburg syndrome, which is characterised by deafness and pigmentation anomalies of eyes, hair, and skin. \nSources: Expert list","entity_name":"PAX3","entity_type":"gene"},{"created":"2025-05-31T11:03:02.155935+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.75","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: SOX10 as ready","entity_name":"SOX10","entity_type":"gene"},{"created":"2025-05-31T11:03:02.146052+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.75","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: sox10 has been classified as Green List (High Evidence).","entity_name":"SOX10","entity_type":"gene"},{"created":"2025-05-31T11:02:56.170294+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.75","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: SOX10 as Green List (high evidence)","entity_name":"SOX10","entity_type":"gene"},{"created":"2025-05-31T11:02:56.163549+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.75","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: sox10 has been classified as Green List (High Evidence).","entity_name":"SOX10","entity_type":"gene"},{"created":"2025-05-31T11:02:49.903165+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.74","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SOX10 was added\ngene: SOX10 was added to Hereditary Pigmentary Disorders. Sources: Expert list\nMode of inheritance for gene: SOX10 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SOX10 were set to 9462749; 18348274; 27863645; 24735604; 27240497; 24311220\nPhenotypes for gene: SOX10 were set to Waardenburg syndrome type 4C MONDO:0013202\nReview for gene: SOX10 was set to GREEN\ngene: SOX10 was marked as current diagnostic\nAdded comment: Heterozygous loss-of-function variants in this gene cause Waardenburg syndrome, which is characterised by deafness and pigmentation anomalies of eyes, hair, and skin. \nSources: Expert list","entity_name":"SOX10","entity_type":"gene"},{"created":"2025-05-31T10:58:25.863025+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.73","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SNAI2 was added\ngene: SNAI2 was added to Hereditary Pigmentary Disorders. Sources: Expert list\nMode of inheritance for gene: SNAI2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: SNAI2 were set to 12444107; 30936914; 12955764; 24443330\nPhenotypes for gene: SNAI2 were set to piebaldism MONDO:0008244; Waardenburg syndrome type 2D MONDO:0012144","entity_name":"SNAI2","entity_type":"gene"},{"created":"2025-05-31T10:53:41.472384+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.72","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: MITF as ready","entity_name":"MITF","entity_type":"gene"},{"created":"2025-05-31T10:53:41.465457+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.72","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: mitf has been classified as Green List (High Evidence).","entity_name":"MITF","entity_type":"gene"},{"created":"2025-05-31T10:53:39.068474+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.72","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: MITF as Green List (high evidence)","entity_name":"MITF","entity_type":"gene"},{"created":"2025-05-31T10:53:39.060461+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.72","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: mitf has been classified as Green List (High Evidence).","entity_name":"MITF","entity_type":"gene"},{"created":"2025-05-31T10:53:30.290403+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.71","user_name":"Bryony Thompson","item_type":"entity","text":"gene: MITF was added\ngene: MITF was added to Hereditary Pigmentary Disorders. Sources: Expert list\nMode of inheritance for gene: MITF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: MITF were set to 7874167; 23512835; 27759048; 28356565\nPhenotypes for gene: MITF were set to Waardenburg syndrome type 2A MONDO:0008671\nReview for gene: MITF was set to GREEN\ngene: MITF was marked as current diagnostic\nAdded comment: Heterozygous loss-of-function variants in this gene cause Waardenburg syndrome, which is characterised by deafness and pigmentation anomalies of eyes, hair, and skin. \nSources: Expert list","entity_name":"MITF","entity_type":"gene"},{"created":"2025-05-30T16:03:58.435936+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.70","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: KIT as ready","entity_name":"KIT","entity_type":"gene"},{"created":"2025-05-30T16:03:58.425423+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.70","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: kit has been classified as Green List (High Evidence).","entity_name":"KIT","entity_type":"gene"},{"created":"2025-05-30T16:03:56.284727+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.70","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: KIT as Green List (high evidence)","entity_name":"KIT","entity_type":"gene"},{"created":"2025-05-30T16:03:56.274719+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.70","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: kit has been classified as Green List (High Evidence).","entity_name":"KIT","entity_type":"gene"},{"created":"2025-05-30T16:03:49.821649+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.69","user_name":"Bryony Thompson","item_type":"entity","text":"gene: KIT was added\ngene: KIT was added to Hereditary Pigmentary Disorders. Sources: Expert list\nMode of inheritance for gene: KIT was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: KIT were set to 1717985; 1384325; 9699740\nPhenotypes for gene: KIT were set to piebaldism MONDO:0008244\nReview for gene: KIT was set to GREEN\ngene: KIT was marked as current diagnostic\nAdded comment: A disorder of pigmentation characterised by patches of white skin and hair. Loss of function is the mechanism of disease. \nSources: Expert list","entity_name":"KIT","entity_type":"gene"},{"created":"2025-05-30T15:54:01.040930+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.68","user_name":"Bryony Thompson","item_type":"panel","text":"Panel status changed from internal to public","entity_name":null,"entity_type":null},{"created":"2025-05-30T15:52:46.981457+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.67","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: XPC as ready","entity_name":"XPC","entity_type":"gene"},{"created":"2025-05-30T15:52:46.974294+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.67","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: xpc has been classified as Green List (High Evidence).","entity_name":"XPC","entity_type":"gene"},{"created":"2025-05-30T15:52:42.590887+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.67","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: XPC as Green List (high evidence)","entity_name":"XPC","entity_type":"gene"},{"created":"2025-05-30T15:52:42.583274+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.67","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: xpc has been classified as Green List (High Evidence).","entity_name":"XPC","entity_type":"gene"},{"created":"2025-05-30T15:52:34.249964+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.66","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: XPA as ready","entity_name":"XPA","entity_type":"gene"},{"created":"2025-05-30T15:52:34.240794+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.66","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: xpa has been classified as Green List (High Evidence).","entity_name":"XPA","entity_type":"gene"},{"created":"2025-05-30T15:52:31.382373+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.66","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: XPA as Green List (high evidence)","entity_name":"XPA","entity_type":"gene"},{"created":"2025-05-30T15:52:31.375570+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.66","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: xpa has been classified as Green List (High Evidence).","entity_name":"XPA","entity_type":"gene"},{"created":"2025-05-30T15:52:23.608776+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.65","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: WRAP53 as ready","entity_name":"WRAP53","entity_type":"gene"},{"created":"2025-05-30T15:52:23.593882+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.65","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: wrap53 has been classified as Green List (High Evidence).","entity_name":"WRAP53","entity_type":"gene"},{"created":"2025-05-30T15:52:21.395900+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.65","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: WRAP53 as Green List (high evidence)","entity_name":"WRAP53","entity_type":"gene"},{"created":"2025-05-30T15:52:21.386300+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.65","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: wrap53 has been classified as Green List (High Evidence).","entity_name":"WRAP53","entity_type":"gene"},{"created":"2025-05-30T15:52:12.227090+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.64","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: TINF2 as ready","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-05-30T15:52:12.220519+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.64","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: tinf2 has been classified as Green List (High Evidence).","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-05-30T15:52:09.385729+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.64","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: TINF2 as Green List (high evidence)","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-05-30T15:52:09.379439+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.64","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: tinf2 has been classified as Green List (High Evidence).","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-05-30T15:52:00.702133+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.63","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: TERT as ready","entity_name":"TERT","entity_type":"gene"},{"created":"2025-05-30T15:52:00.695538+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.63","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: tert has been classified as Green List (High Evidence).","entity_name":"TERT","entity_type":"gene"},{"created":"2025-05-30T15:51:58.707240+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.63","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: TERT as Green List (high evidence)","entity_name":"TERT","entity_type":"gene"},{"created":"2025-05-30T15:51:58.700024+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.63","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: tert has been classified as Green List (High Evidence).","entity_name":"TERT","entity_type":"gene"},{"created":"2025-05-30T15:51:50.907093+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.62","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: TERC as ready","entity_name":"TERC","entity_type":"gene"},{"created":"2025-05-30T15:51:50.900954+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.62","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: terc has been classified as Green List (High Evidence).","entity_name":"TERC","entity_type":"gene"},{"created":"2025-05-30T15:51:48.797248+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.62","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: TERC as Green List (high evidence)","entity_name":"TERC","entity_type":"gene"},{"created":"2025-05-30T15:51:48.786010+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.62","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: terc has been classified as Green List (High Evidence).","entity_name":"TERC","entity_type":"gene"},{"created":"2025-05-30T15:51:36.984818+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.61","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: SASH1 as ready","entity_name":"SASH1","entity_type":"gene"},{"created":"2025-05-30T15:51:36.975133+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.61","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: sash1 has been classified as Green List (High Evidence).","entity_name":"SASH1","entity_type":"gene"},{"created":"2025-05-30T15:51:33.989702+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.61","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: SASH1 as Green List (high evidence)","entity_name":"SASH1","entity_type":"gene"},{"created":"2025-05-30T15:51:33.982602+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.61","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: sash1 has been classified as Green List (High Evidence).","entity_name":"SASH1","entity_type":"gene"},{"created":"2025-05-30T15:51:25.492833+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.60","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: RTEL1 as ready","entity_name":"RTEL1","entity_type":"gene"},{"created":"2025-05-30T15:51:25.485131+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.60","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: rtel1 has been classified as Green List (High Evidence).","entity_name":"RTEL1","entity_type":"gene"},{"created":"2025-05-30T15:51:22.696159+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.60","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: RTEL1 as Green List (high evidence)","entity_name":"RTEL1","entity_type":"gene"},{"created":"2025-05-30T15:51:22.689377+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.60","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: rtel1 has been classified as Green List (High Evidence).","entity_name":"RTEL1","entity_type":"gene"},{"created":"2025-05-30T15:51:13.791741+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.59","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: RPA1 as ready","entity_name":"RPA1","entity_type":"gene"},{"created":"2025-05-30T15:51:13.771348+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.59","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: rpa1 has been classified as Green List (High Evidence).","entity_name":"RPA1","entity_type":"gene"},{"created":"2025-05-30T15:51:10.095671+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.59","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: RPA1 as Green List (high evidence)","entity_name":"RPA1","entity_type":"gene"},{"created":"2025-05-30T15:51:10.088319+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.59","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: rpa1 has been classified as Green List (High Evidence).","entity_name":"RPA1","entity_type":"gene"},{"created":"2025-05-30T15:51:02.453362+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.58","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: PSENEN as ready","entity_name":"PSENEN","entity_type":"gene"},{"created":"2025-05-30T15:51:02.442593+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.58","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: psenen has been classified as Green List (High Evidence).","entity_name":"PSENEN","entity_type":"gene"},{"created":"2025-05-30T15:50:59.287120+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.58","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: PSENEN as Green List (high evidence)","entity_name":"PSENEN","entity_type":"gene"},{"created":"2025-05-30T15:50:59.280250+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.58","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: psenen has been classified as Green List (High Evidence).","entity_name":"PSENEN","entity_type":"gene"},{"created":"2025-05-30T15:50:51.259604+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.57","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: POLH as ready","entity_name":"POLH","entity_type":"gene"},{"created":"2025-05-30T15:50:51.249788+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.57","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: polh has been classified as Green List (High Evidence).","entity_name":"POLH","entity_type":"gene"},{"created":"2025-05-30T15:50:48.540229+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.57","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: POLH as Green List (high evidence)","entity_name":"POLH","entity_type":"gene"},{"created":"2025-05-30T15:50:48.533384+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.57","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: polh has been classified as Green List (High Evidence).","entity_name":"POLH","entity_type":"gene"},{"created":"2025-05-30T15:50:40.122788+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.56","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: POGLUT1 as ready","entity_name":"POGLUT1","entity_type":"gene"},{"created":"2025-05-30T15:50:40.113112+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.56","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: poglut1 has been classified as Green List (High Evidence).","entity_name":"POGLUT1","entity_type":"gene"},{"created":"2025-05-30T15:50:37.383071+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.56","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: POGLUT1 as Green List (high evidence)","entity_name":"POGLUT1","entity_type":"gene"},{"created":"2025-05-30T15:50:37.373353+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.56","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: poglut1 has been classified as Green List (High Evidence).","entity_name":"POGLUT1","entity_type":"gene"},{"created":"2025-05-30T15:50:29.935508+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: POFUT1 as ready","entity_name":"POFUT1","entity_type":"gene"},{"created":"2025-05-30T15:50:29.929336+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: pofut1 has been classified as Green List (High Evidence).","entity_name":"POFUT1","entity_type":"gene"},{"created":"2025-05-30T15:50:26.511904+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: POFUT1 as Green List (high evidence)","entity_name":"POFUT1","entity_type":"gene"},{"created":"2025-05-30T15:50:26.503776+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.55","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: pofut1 has been classified as Green List (High Evidence).","entity_name":"POFUT1","entity_type":"gene"},{"created":"2025-05-30T15:50:18.654056+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: PARN as ready","entity_name":"PARN","entity_type":"gene"},{"created":"2025-05-30T15:50:18.647533+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: parn has been classified as Green List (High Evidence).","entity_name":"PARN","entity_type":"gene"},{"created":"2025-05-30T15:50:16.235520+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: PARN as Green List (high evidence)","entity_name":"PARN","entity_type":"gene"},{"created":"2025-05-30T15:50:16.228211+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.54","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: parn has been classified as Green List (High Evidence).","entity_name":"PARN","entity_type":"gene"},{"created":"2025-05-30T15:50:04.739752+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.53","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: NOP10 as ready","entity_name":"NOP10","entity_type":"gene"},{"created":"2025-05-30T15:50:04.732852+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.53","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: nop10 has been classified as Amber List (Moderate Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2025-05-30T15:50:00.583333+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.53","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: NOP10 as Amber List (moderate evidence)","entity_name":"NOP10","entity_type":"gene"},{"created":"2025-05-30T15:50:00.575129+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.53","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: nop10 has been classified as Amber List (Moderate Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2025-05-30T15:49:50.385502+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.52","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: NHP2 as ready","entity_name":"NHP2","entity_type":"gene"},{"created":"2025-05-30T15:49:50.378564+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.52","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: nhp2 has been classified as Green List (High Evidence).","entity_name":"NHP2","entity_type":"gene"},{"created":"2025-05-30T15:49:47.441456+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.52","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: NHP2 as Green List (high evidence)","entity_name":"NHP2","entity_type":"gene"},{"created":"2025-05-30T15:49:47.434918+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.52","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: nhp2 has been classified as Green List (High Evidence).","entity_name":"NHP2","entity_type":"gene"},{"created":"2025-05-30T15:49:39.286969+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.51","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: KRT5 as ready","entity_name":"KRT5","entity_type":"gene"},{"created":"2025-05-30T15:49:39.279910+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.51","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: krt5 has been classified as Green List (High Evidence).","entity_name":"KRT5","entity_type":"gene"},{"created":"2025-05-30T15:49:36.999825+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.51","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: KRT5 as Green List (high evidence)","entity_name":"KRT5","entity_type":"gene"},{"created":"2025-05-30T15:49:36.992646+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.51","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: krt5 has been classified as Green List (High Evidence).","entity_name":"KRT5","entity_type":"gene"},{"created":"2025-05-30T15:49:27.760806+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.50","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: KRT14 as ready","entity_name":"KRT14","entity_type":"gene"},{"created":"2025-05-30T15:49:27.751102+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.50","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: krt14 has been classified as Green List (High Evidence).","entity_name":"KRT14","entity_type":"gene"},{"created":"2025-05-30T15:49:24.498388+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.50","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: KRT14 as Green List (high evidence)","entity_name":"KRT14","entity_type":"gene"},{"created":"2025-05-30T15:49:24.491618+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.50","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: krt14 has been classified as Green List (High Evidence).","entity_name":"KRT14","entity_type":"gene"},{"created":"2025-05-30T15:48:15.288854+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.49","user_name":"Bryony Thompson","item_type":"entity","text":"Marked gene: KITLG as ready","entity_name":"KITLG","entity_type":"gene"},{"created":"2025-05-30T15:48:15.279131+10:00","panel_name":"Hereditary Pigmentary Disorders","panel_id":4457,"panel_version":"0.49","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: kitlg has been classified as Green List (High Evidence).","entity_name":"KITLG","entity_type":"gene"}]}