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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=216",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}