HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220725,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2017",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2015",
"results": [
{
"created": "2019-12-31T15:58:05.190521+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cldn9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:57:57.316285+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLDN9 as Amber List (moderate evidence)",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:57:57.304581+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cldn9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:57:36.596542+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CLDN9 was added\ngene: CLDN9 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: CLDN9 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CLDN9 were set to 31175426; 19696885\nPhenotypes for gene: CLDN9 were set to Deafness, autosomal recessive\nReview for gene: CLDN9 was set to AMBER\nAdded comment: Single family with multiple sibs reported; mouse model exhibits deafness. \nSources: Literature",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:57:04.573290+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLDN9 as ready",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:57:04.561543+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cldn9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:55:19.046183+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLDN9 were changed from to Deafness, autosomal recessive",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:54:50.491467+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLDN9 as Amber List (moderate evidence)",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:54:50.478815+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cldn9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:54:19.636378+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CLDN9 was added\ngene: CLDN9 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: CLDN9 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CLDN9 were set to 31175426; 19696885\nReview for gene: CLDN9 was set to AMBER\nAdded comment: Single family with multiple sibs reported; mouse model exhibits deafness. \nSources: Literature",
"entity_name": "CLDN9",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:50.184329+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TOP2B as ready",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:50.171046+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: top2b has been classified as Amber List (Moderate Evidence).",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:40.902354+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TOP2B as ready",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:40.886101+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: top2b has been classified as Amber List (Moderate Evidence).",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:40.590631+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TOP2B as Amber List (moderate evidence)",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:40.575202+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: top2b has been classified as Amber List (Moderate Evidence).",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:36.943994+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TOP2B as Amber List (moderate evidence)",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:36.928474+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: top2b has been classified as Amber List (Moderate Evidence).",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:49:08.822784+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TOP2B was added\ngene: TOP2B was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: TOP2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TOP2B were set to 31198993\nPhenotypes for gene: TOP2B were set to Autosomal dominant deafness\nReview for gene: TOP2B was set to AMBER\nAdded comment: One multigenerational family where variant in this gene segregated; two additional variants identified in a cohort; supportive animal model data. \nSources: Literature",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:46:54.427238+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TOP2B was added\ngene: TOP2B was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: TOP2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TOP2B were set to 31198993\nPhenotypes for gene: TOP2B were set to Autosomal dominant deafness\nReview for gene: TOP2B was set to AMBER\nAdded comment: One multigenerational family where variant in this gene segregated; two additional variants identified in a cohort; supportive animal model data. \nSources: Literature",
"entity_name": "TOP2B",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:39:39.240447+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCAP31 as ready",
"entity_name": "BCAP31",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:39:39.227378+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bcap31 has been classified as Green List (High Evidence).",
"entity_name": "BCAP31",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:39:09.781277+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BCAP31 as Green List (high evidence)",
"entity_name": "BCAP31",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:39:09.753836+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bcap31 has been classified as Green List (High Evidence).",
"entity_name": "BCAP31",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:38:33.963225+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BCAP31 was added\ngene: BCAP31 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: BCAP31 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: BCAP31 were set to 24011989; 31330203; 28332767\nPhenotypes for gene: BCAP31 were set to Deafness, dystonia, and cerebral hypomyelination, MIM#\t300475\nReview for gene: BCAP31 was set to GREEN\nAdded comment: Five unrelated families reported, deafness is part of the phenotype. \nSources: Literature",
"entity_name": "BCAP31",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:28:27.474408+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AP1B1 as ready",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:28:27.463605+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1b1 has been classified as Green List (High Evidence).",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:28:22.806712+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AP1B1 as Green List (high evidence)",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:28:22.795233+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1b1 has been classified as Green List (High Evidence).",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:26:30.226407+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AP1B1 was added\ngene: AP1B1 was added to Ichthyosis_VCGS. Sources: Literature\nMode of inheritance for gene: AP1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1B1 were set to 31630788; 31630791\nPhenotypes for gene: AP1B1 were set to Intellectual disability; enteropathy; deafness; ichthyosis; keratoderma\nReview for gene: AP1B1 was set to GREEN\nAdded comment: Four unrelated families with bi-allelic LoF variants in this gene. \nSources: Literature",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:24:09.193297+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AP1B1 as ready",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:24:09.179394+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1b1 has been classified as Green List (High Evidence).",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:24:00.124229+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1454",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AP1B1 as Green List (high evidence)",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:24:00.112955+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1454",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1b1 has been classified as Green List (High Evidence).",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:23:44.163466+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AP1B1 as Green List (high evidence)",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:23:44.151581+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1b1 has been classified as Green List (High Evidence).",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:23:29.335518+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AP1B1 was added\ngene: AP1B1 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: AP1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1B1 were set to 31630788; 31630791\nPhenotypes for gene: AP1B1 were set to Intellectual disability; enteropathy; deafness; ichthyosis; keratoderma\nReview for gene: AP1B1 was set to GREEN\nAdded comment: Four unrelated families with bi-allelic LoF variants in this gene. \nSources: Literature",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:21:59.080857+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AP1B1 was added\ngene: AP1B1 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: AP1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1B1 were set to 31630788; 31630791\nPhenotypes for gene: AP1B1 were set to Intellectual disability; enteropathy; deafness; ichthyosis; keratoderma\nReview for gene: AP1B1 was set to GREEN\nAdded comment: Four unrelated families with bi-allelic LoF variants in this gene. \nSources: Literature",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:18:59.284638+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AP1B1 as ready",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:18:59.272603+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1b1 has been classified as Green List (High Evidence).",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:18:52.916696+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AP1B1 were changed from Intellectual disability; enteropathy; deafness; peripheral neuropathy; ichthyosis; keratoderma to Intellectual disability; enteropathy; deafness; ichthyosis; keratoderma",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:17:18.396633+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AP1B1 as Green List (high evidence)",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:17:18.385664+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1b1 has been classified as Green List (High Evidence).",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:16:44.649147+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AP1B1 was added\ngene: AP1B1 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: AP1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1B1 were set to 31630788; 31630791\nPhenotypes for gene: AP1B1 were set to Intellectual disability; enteropathy; deafness; peripheral neuropathy; ichthyosis; keratoderma\nReview for gene: AP1B1 was set to GREEN\nAdded comment: Four families reported with bi-allelic LoF variants in this gene. \nSources: Literature",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:08:32.965667+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.506",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADCY1 as ready",
"entity_name": "ADCY1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:08:32.953307+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.506",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adcy1 has been classified as Red List (Low Evidence).",
"entity_name": "ADCY1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:08:24.993517+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.506",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ADCY1 were set to ",
"entity_name": "ADCY1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:08:03.551892+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.505",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADCY1 were changed from to Deafness, autosomal recessive 44, MIM# 610154",
"entity_name": "ADCY1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:07:40.637195+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADCY1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADCY1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:06:51.548951+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ADCY1 as Red List (low evidence)",
"entity_name": "ADCY1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:06:51.536039+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adcy1 has been classified as Red List (Low Evidence).",
"entity_name": "ADCY1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:06:34.568396+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ADCY1: Rating: RED; Mode of pathogenicity: None; Publications: 24482543; Phenotypes: Deafness, autosomal recessive 44, MIM# 610154; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADCY1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:02:47.578255+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BDP1 as ready",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:02:47.565282+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bdp1 has been classified as Red List (Low Evidence).",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:02:38.937058+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BDP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:02:24.471649+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BDP1 were changed from to Deafness, autosomal recessive 112, MIM#618257",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:02:11.420849+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BDP1 were set to ",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:01:45.630655+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BDP1 as Red List (low evidence)",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:01:45.616816+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bdp1 has been classified as Red List (Low Evidence).",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T15:01:27.132008+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BDP1: Rating: RED; Mode of pathogenicity: None; Publications: 24312468, 25060281; Phenotypes: Deafness, autosomal recessive 112, MIM#618257; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:59:58.820505+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BDP1 as ready",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:59:58.807958+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bdp1 has been classified as Red List (Low Evidence).",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:59:55.807576+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BDP1 were changed from to Deafness, autosomal recessive 112, MIM#618257",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:59:32.089481+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BDP1 were set to ",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:59:07.296510+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BDP1 as Red List (low evidence)",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:59:07.290803+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Single family, nonstop variant.",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:59:07.242651+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bdp1 has been classified as Red List (Low Evidence).",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:54:46.980679+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BDP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BDP1",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:52:23.593718+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CCDC50 as ready",
"entity_name": "CCDC50",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:52:23.582513+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ccdc50 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CCDC50",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:52:15.204042+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CCDC50 were set to ",
"entity_name": "CCDC50",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:51:45.947987+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CCDC50 were changed from to Deafness, autosomal dominant 44, MIM#\t607453; Childhood onset deafness, progressive",
"entity_name": "CCDC50",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:51:06.081950+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CCDC50 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CCDC50",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:50:28.832815+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CCDC50 as Amber List (moderate evidence)",
"entity_name": "CCDC50",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:50:28.819936+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ccdc50 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CCDC50",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:49:21.231156+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLIC5 were changed from to Deafness, autosomal recessive 103, MIM# 616042",
"entity_name": "CLIC5",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:48:35.104310+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.497",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CLIC5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CLIC5",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:47:48.241622+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLIC5 were set to ",
"entity_name": "CLIC5",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:47:29.773345+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLIC5 as Amber List (moderate evidence)",
"entity_name": "CLIC5",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:47:29.761172+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clic5 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CLIC5",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:47:10.255543+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CLIC5: Rating: AMBER; Mode of pathogenicity: None; Publications: 24781754, 17021174; Phenotypes: Deafness, autosomal recessive 103, MIM# 616042; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CLIC5",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:44:52.471151+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CEP78 as ready",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:44:52.458691+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep78 has been classified as Green List (High Evidence).",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:44:45.383235+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CEP78 were changed from Cone-rod dystrophy and hearing loss to Cone-rod dystrophy and hearing loss, MIM#617236",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:44:14.924790+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CEP78 as Green List (high evidence)",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:44:14.912964+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep78 has been classified as Green List (High Evidence).",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:40:10.626155+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYM as ready",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:40:10.613707+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crym has been classified as Amber List (Moderate Evidence).",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:40:06.660241+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYM was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:38:55.505546+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYM were changed from Deafness, autosomal dominant 40, MIM#\t616357 to Deafness, autosomal dominant 40, MIM#\t616357",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:32:52.197915+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYM was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:32:30.983751+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYM was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:32:07.326898+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYM were changed from to Deafness, autosomal dominant 40, MIM#\t616357",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:31:43.123036+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYM were set to 12471561; 16740909; 18448257; 24676347; 26915689",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:31:30.529388+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DIABLO as ready",
"entity_name": "DIABLO",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:31:30.516499+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: diablo has been classified as Red List (Low Evidence).",
"entity_name": "DIABLO",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:31:19.548122+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYM were set to ",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:31:16.242187+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DIABLO were changed from to Deafness, autosomal dominant 64, MIM# 614152",
"entity_name": "DIABLO",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:30:42.536572+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CRYM as Amber List (moderate evidence)",
"entity_name": "CRYM",
"entity_type": "gene"
},
{
"created": "2019-12-31T14:30:42.523382+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crym has been classified as Amber List (Moderate Evidence).",
"entity_name": "CRYM",
"entity_type": "gene"
}
]
}