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{
"count": 220423,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2034",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2032",
"results": [
{
"created": "2019-12-19T12:13:13.947301+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pls1 has been classified as Green List (High Evidence).",
"entity_name": "PLS1",
"entity_type": "gene"
},
{
"created": "2019-12-19T12:13:09.355775+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PLS1 as Green List (high evidence)",
"entity_name": "PLS1",
"entity_type": "gene"
},
{
"created": "2019-12-19T12:13:09.348934+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pls1 has been classified as Green List (High Evidence).",
"entity_name": "PLS1",
"entity_type": "gene"
},
{
"created": "2019-12-19T12:12:40.990093+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLS1 was added\ngene: PLS1 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: PLS1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PLS1 were set to 31397523; 31432506; 30872814\nPhenotypes for gene: PLS1 were set to Deafness\nReview for gene: PLS1 was set to GREEN\nAdded comment: Non-syndromic deafness in 5 families with mono allelic variants in this gene. Mouse model. \nSources: Literature",
"entity_name": "PLS1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:59:07.113314+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.367",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TASP1 as ready",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:59:07.105919+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.367",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tasp1 has been classified as Green List (High Evidence).",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:58:56.278826+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.367",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TASP1 as Green List (high evidence)",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:58:56.271994+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.367",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tasp1 has been classified as Green List (High Evidence).",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:58:32.626126+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TASP1 was added\ngene: TASP1 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: TASP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TASP1 were set to 31209944; 31350873\nPhenotypes for gene: TASP1 were set to Developmental delay; microcephaly; dysmorphic features; congenital abnormalities\nReview for gene: TASP1 was set to GREEN\nAdded comment: Four unrelated families reported; two with founder mutation. Protein interacts with KMT2A and KMT2D. Another infant with a de novo missense variant reported in a single infant with multiple congenital abnormalities, insufficient evidence for mono allelic disease at present. \nSources: Literature",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:56:25.499065+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TASP1 as ready",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:56:25.492148+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tasp1 has been classified as Green List (High Evidence).",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:56:17.652642+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TASP1 as Green List (high evidence)",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:56:17.646006+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tasp1 has been classified as Green List (High Evidence).",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:56:05.368258+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TASP1 was added\ngene: TASP1 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: TASP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TASP1 were set to 31209944; 31350873\nPhenotypes for gene: TASP1 were set to Developmental delay; microcephaly; dysmorphic features; congenital abnormalities\nReview for gene: TASP1 was set to GREEN\nAdded comment: Four unrelated families reported; two with founder mutation. Protein interacts with KMT2A and KMT2D. Another infant with a de novo missense variant reported in a single infant with multiple congenital abnormalities, insufficient evidence for mono allelic disease at present. \nSources: Literature",
"entity_name": "TASP1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:44:29.756780+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.365",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FST was added\ngene: FST was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: FST was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: FST were set to 31215115\nPhenotypes for gene: FST were set to Cleft lip and palate\nReview for gene: FST was set to RED\nAdded comment: Single family reported. \nSources: Literature",
"entity_name": "FST",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:36:32.334422+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.364",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GDF11 as ready",
"entity_name": "GDF11",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:36:32.327597+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.364",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gdf11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GDF11",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:36:22.796370+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.364",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GDF11 as Amber List (moderate evidence)",
"entity_name": "GDF11",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:36:22.787723+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.364",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gdf11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GDF11",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:36:03.526041+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GDF11 was added\ngene: GDF11 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: GDF11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: GDF11 were set to 31215115\nPhenotypes for gene: GDF11 were set to Cleft lip and palate\nReview for gene: GDF11 was set to AMBER\nAdded comment: Cleft lip and palate, and rib and vertebral hypersegmentation in a single family. Mouse model. \nSources: Literature",
"entity_name": "GDF11",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:06:39.379366+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.7",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Classified gene: MLC1 as Green List (high evidence)",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T11:06:39.371744+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.7",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Gene: mlc1 has been classified as Green List (High Evidence).",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T10:41:10.931885+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.6",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Marked gene: MLC1 as ready",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T10:41:10.924824+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.6",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Gene: mlc1 has been classified as Red List (Low Evidence).",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T10:40:42.841000+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.6",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "reviewed gene: MLC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11254442, 18757878, 16652334; Phenotypes: Megalencephalic leukoencephalopathy with subcortical cysts OMIM#604004; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T10:19:09.148357+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.5",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "gene: MLC1 was added\ngene: MLC1 was added to Macrocephaly/Megalencephaly_VCGS. Sources: Literature\nMode of inheritance for gene: MLC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MLC1 were set to 11254442; 18757878; 16652334\nPhenotypes for gene: MLC1 were set to Megalencephalic leukoencephalopathy with subcortical cysts OMIM#604004\nPenetrance for gene: MLC1 were set to Complete",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T09:59:43.671094+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.4",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Marked gene: HERC1 as ready",
"entity_name": "HERC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T09:59:43.663616+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.4",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Gene: herc1 has been classified as Green List (High Evidence).",
"entity_name": "HERC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T09:59:26.346720+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.4",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Classified gene: HERC1 as Green List (high evidence)",
"entity_name": "HERC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T09:59:26.339544+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.4",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Gene: herc1 has been classified as Green List (High Evidence).",
"entity_name": "HERC1",
"entity_type": "gene"
},
{
"created": "2019-12-19T09:58:22.103958+11:00",
"panel_name": "Macrocephaly/Megalencephaly_VCGS",
"panel_id": 135,
"panel_version": "0.3",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "gene: HERC1 was added\ngene: HERC1 was added to Macrocephaly/Megalencephaly_VCGS. Sources: Literature\nMode of inheritance for gene: HERC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HERC1 were set to 27108999; 26153217; 26138117\nPhenotypes for gene: HERC1 were set to MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION OMIM#617011\nPenetrance for gene: HERC1 were set to Complete\nReview for gene: HERC1 was set to GREEN\nAdded comment: Sources: Literature",
"entity_name": "HERC1",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:37:12.487714+11:00",
"panel_name": "Disorders of Sex Differentiation_VCGS",
"panel_id": 99,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PBX1 as ready",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:37:12.481023+11:00",
"panel_name": "Disorders of Sex Differentiation_VCGS",
"panel_id": 99,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pbx1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:37:07.961327+11:00",
"panel_name": "Disorders of Sex Differentiation_VCGS",
"panel_id": 99,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PBX1 as Amber List (moderate evidence)",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:37:07.953142+11:00",
"panel_name": "Disorders of Sex Differentiation_VCGS",
"panel_id": 99,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pbx1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:36:38.526886+11:00",
"panel_name": "Disorders of Sex Differentiation_VCGS",
"panel_id": 99,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PBX1 was added\ngene: PBX1 was added to Disorders of Sex Differentiation_VCGS. Sources: Literature\nMode of inheritance for gene: PBX1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PBX1 were set to 31302614; 31058389\nPhenotypes for gene: PBX1 were set to 46, XY gonadal dysgenesis\nReview for gene: PBX1 was set to AMBER\nAdded comment: Two individuals reported with mono allelic variants in this gene and 46,XY gonadal dysgenesis. \nSources: Literature",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:28:38.254768+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNA2 as ready",
"entity_name": "DNA2",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:28:38.247118+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dna2 has been classified as Green List (High Evidence).",
"entity_name": "DNA2",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:28:30.424528+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNA2 were changed from to Seckel syndrome 8, MIM#615807",
"entity_name": "DNA2",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:27:57.730921+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DNA2 were set to ",
"entity_name": "DNA2",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:27:26.512620+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DNA2",
"entity_type": "gene"
},
{
"created": "2019-12-18T18:26:54.199852+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DNA2: Rating: GREEN; Mode of pathogenicity: None; Publications: 24389050, 31045292; Phenotypes: Seckel syndrome 8, MIM#615807; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DNA2",
"entity_type": "gene"
},
{
"created": "2019-12-18T14:50:13.439961+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1425",
"user_name": "Chris Richmond",
"item_type": "entity",
"text": "reviewed gene: CACNA1G: Rating: ; Mode of pathogenicity: Other; Publications: 29878067, 31836334; Phenotypes: Spinocerebellar ataxia 42 [616795], Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits [618087], Infantile-Onset Syndromic Cerebellar Ataxia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:52:39.431348+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SOST as ready",
"entity_name": "SOST",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:52:39.424632+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sost has been classified as Red List (Low Evidence).",
"entity_name": "SOST",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:52:34.835880+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SOST was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "SOST",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:19:46.882296+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HNRNPR as ready",
"entity_name": "HNRNPR",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:19:46.875547+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpr has been classified as Green List (High Evidence).",
"entity_name": "HNRNPR",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:19:35.588903+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HNRNPR as Green List (high evidence)",
"entity_name": "HNRNPR",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:19:35.581960+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnrnpr has been classified as Green List (High Evidence).",
"entity_name": "HNRNPR",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:19:05.401882+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1423",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HNRNPR was added\ngene: HNRNPR was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: HNRNPR was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: HNRNPR were set to 31079900\nPhenotypes for gene: HNRNPR were set to Intellectual disability; seizures; dysmorphic features\nReview for gene: HNRNPR was set to GREEN\nAdded comment: Four unrelated families with heterozygous variants in this gene and a neurodevelopmental phenotype. \nSources: Literature",
"entity_name": "HNRNPR",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:09:40.551188+11:00",
"panel_name": "Hereditary Haemorrhagic Telangiectasia_RMH",
"panel_id": 260,
"panel_version": "0.1",
"user_name": "Bryony Thompson",
"item_type": "panel",
"text": "Panel status changed from internal to public",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-18T12:06:26.122570+11:00",
"panel_name": "Hereditary Haemorrhagic Telangiectasia_RMH",
"panel_id": 260,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: SMAD4 was added\ngene: SMAD4 was added to Hereditary Haemorrhagic Telangiectasia_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: SMAD4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SMAD4 were set to Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome, 175050",
"entity_name": "SMAD4",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:06:26.074690+11:00",
"panel_name": "Hereditary Haemorrhagic Telangiectasia_RMH",
"panel_id": 260,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: RASA1 was added\ngene: RASA1 was added to Hereditary Haemorrhagic Telangiectasia_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: RASA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: RASA1 were set to Capillary malformation-arteriovenous malformation 608354",
"entity_name": "RASA1",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:06:25.989556+11:00",
"panel_name": "Hereditary Haemorrhagic Telangiectasia_RMH",
"panel_id": 260,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GDF2 was added\ngene: GDF2 was added to Hereditary Haemorrhagic Telangiectasia_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: GDF2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: GDF2 were set to Telangiectasia, hereditary hemorrhagic, type 5 615506",
"entity_name": "GDF2",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:06:25.939925+11:00",
"panel_name": "Hereditary Haemorrhagic Telangiectasia_RMH",
"panel_id": 260,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: EPHB4 was added\ngene: EPHB4 was added to Hereditary Haemorrhagic Telangiectasia_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: EPHB4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: EPHB4 were set to Capillary malformation-arteriovenous malformation-2",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:06:25.888916+11:00",
"panel_name": "Hereditary Haemorrhagic Telangiectasia_RMH",
"panel_id": 260,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ENG was added\ngene: ENG was added to Hereditary Haemorrhagic Telangiectasia_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: ENG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: ENG were set to Telangiectasia, hereditary hemorrhagic, type 1, 187300; Gastrointestinal telangiectasia (HP:0002604); Palate telangiectasia (HP:0002707); Lip telangiectasia (HP:0000214); Pulmonary arteriovenous malformation (HP:0006548); Nasal mucosa telangiectasia (HP:0000434); Tongue telangiectasia (HP:0000227); Epistaxis (HP:0000421); Cerebral arteriovenous malformation (HP:0002408); Hepatic arteriovenous malformation (HP:0006574; Spinal arteriovenous malformation (HP:0002390); ); Finger pad telangiectasia (pulp not nail side); Arteriovenous malformation (HP:0100026)",
"entity_name": "ENG",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:06:25.836820+11:00",
"panel_name": "Hereditary Haemorrhagic Telangiectasia_RMH",
"panel_id": 260,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ACVRL1 was added\ngene: ACVRL1 was added to Hereditary Haemorrhagic Telangiectasia_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: ACVRL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: ACVRL1 were set to telangiectasia; pulmonary arterial hypertension; epistaxis; pulmonary arteriovenous malformation; cerebral pulmonary arteriovenous malformation; hepatic arteriovenous malformation; Telangiectasia, hereditary hemorrhagic, type 2 600376",
"entity_name": "ACVRL1",
"entity_type": "gene"
},
{
"created": "2019-12-18T12:06:25.805259+11:00",
"panel_name": "Hereditary Haemorrhagic Telangiectasia_RMH",
"panel_id": 260,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "panel",
"text": "Added panel Hereditary Haemorrhagic Telangiectasia_RMH",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-18T11:05:07.238239+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRDM13 as ready",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2019-12-18T11:05:07.231297+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prdm13 has been classified as Green List (High Evidence).",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2019-12-18T11:04:15.909640+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRDM13 as Green List (high evidence)",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2019-12-18T11:04:15.902764+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prdm13 has been classified as Green List (High Evidence).",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2019-12-18T11:03:57.099894+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.361",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PRDM13 was added\ngene: PRDM13 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: PRDM13 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PRDM13 were set to 30710461\nPhenotypes for gene: PRDM13 were set to Retinal dystrophy\nMode of pathogenicity for gene: PRDM13 was set to Other\nReview for gene: PRDM13 was set to GREEN\nAdded comment: 8 individuals from three families reported with UPSTREAM NON-CODING variants in this gene. \nSources: Literature",
"entity_name": "PRDM13",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:40:42.829398+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.360",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MICB as ready",
"entity_name": "MICB",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:40:42.824744+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.360",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Agree, cannot find evidence for Mendelian gene-disease association.",
"entity_name": "MICB",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:40:42.796337+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.360",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: micb has been classified as Red List (Low Evidence).",
"entity_name": "MICB",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:40:28.617461+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.360",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MICB as Red List (low evidence)",
"entity_name": "MICB",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:40:28.609582+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.360",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: micb has been classified as Red List (Low Evidence).",
"entity_name": "MICB",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:29:04.194938+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel status changed from internal to public",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-18T10:26:55.398631+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNJ2 was added\ngene: KCNJ2 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: KCNJ2 was set to Unknown",
"entity_name": "KCNJ2",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:55.344419+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CACNA1S was added\ngene: CACNA1S was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: CACNA1S was set to Unknown",
"entity_name": "CACNA1S",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:55.290423+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNMA1 was added\ngene: KCNMA1 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: KCNMA1 was set to Unknown",
"entity_name": "KCNMA1",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:55.233122+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SCN4A was added\ngene: SCN4A was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: SCN4A was set to Unknown",
"entity_name": "SCN4A",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.993348+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SPR was added\ngene: SPR was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: SPR was set to Unknown",
"entity_name": "SPR",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.939237+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC6A5 was added\ngene: SLC6A5 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: SLC6A5 was set to Unknown",
"entity_name": "SLC6A5",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.885056+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC2A1 was added\ngene: SLC2A1 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: SLC2A1 was set to Unknown",
"entity_name": "SLC2A1",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.812335+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC1A3 was added\ngene: SLC1A3 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: SLC1A3 was set to Unknown",
"entity_name": "SLC1A3",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.756104+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SCN8A was added\ngene: SCN8A was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: SCN8A was set to Unknown",
"entity_name": "SCN8A",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.702840+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SCN2A was added\ngene: SCN2A was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: SCN2A was set to Unknown",
"entity_name": "SCN2A",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.647999+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SCN1A was added\ngene: SCN1A was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: SCN1A was set to Unknown",
"entity_name": "SCN1A",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.592847+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PRRT2 was added\ngene: PRRT2 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: PRRT2 was set to Unknown",
"entity_name": "PRRT2",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.539402+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PNKD was added\ngene: PNKD was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: PNKD was set to Unknown",
"entity_name": "PNKD",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.485635+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNQ3 was added\ngene: KCNQ3 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: KCNQ3 was set to Unknown",
"entity_name": "KCNQ3",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.433504+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNQ2 was added\ngene: KCNQ2 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: KCNQ2 was set to Unknown",
"entity_name": "KCNQ2",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.380604+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNA2 was added\ngene: KCNA2 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: KCNA2 was set to Unknown",
"entity_name": "KCNA2",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.328376+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNA1 was added\ngene: KCNA1 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: KCNA1 was set to Unknown",
"entity_name": "KCNA1",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.276194+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GLRB was added\ngene: GLRB was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: GLRB was set to Unknown",
"entity_name": "GLRB",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.222980+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GLRA1 was added\ngene: GLRA1 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: GLRA1 was set to Unknown",
"entity_name": "GLRA1",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.171192+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GNAO1 was added\ngene: GNAO1 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: GNAO1 was set to Unknown",
"entity_name": "GNAO1",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:54.117869+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CACNB4 was added\ngene: CACNB4 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: CACNB4 was set to Unknown",
"entity_name": "CACNB4",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:53.995578+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CACNA1A was added\ngene: CACNA1A was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: CACNA1A was set to Unknown",
"entity_name": "CACNA1A",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:53.943780+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ATP7B was added\ngene: ATP7B was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: ATP7B was set to Unknown",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:53.890329+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ATP1A3 was added\ngene: ATP1A3 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: ATP1A3 was set to Unknown",
"entity_name": "ATP1A3",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:53.838552+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ATP1A2 was added\ngene: ATP1A2 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: ATP1A2 was set to Unknown",
"entity_name": "ATP1A2",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:53.783765+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ADCY5 was added\ngene: ADCY5 was added to Paroxysmal dyskinesia_VCGS. Sources: Victorian Clinical Genetics Services,Expert Review Green,Royal Children's Hospital Neurology Department\nMode of inheritance for gene: ADCY5 was set to Unknown",
"entity_name": "ADCY5",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:26:53.741177+11:00",
"panel_name": "Paroxysmal dyskinesia_VCGS",
"panel_id": 259,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Paroxysmal dyskinesia_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-18T10:12:45.994075+11:00",
"panel_name": "Autism_VCGS",
"panel_id": 51,
"panel_version": "0.15",
"user_name": "Natasha Brown",
"item_type": "entity",
"text": "Marked gene: DSCAM as ready",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:12:45.987474+11:00",
"panel_name": "Autism_VCGS",
"panel_id": 51,
"panel_version": "0.15",
"user_name": "Natasha Brown",
"item_type": "entity",
"text": "Gene: dscam has been classified as Green List (High Evidence).",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2019-12-18T10:12:23.248090+11:00",
"panel_name": "Autism_VCGS",
"panel_id": 51,
"panel_version": "0.15",
"user_name": "Natasha Brown",
"item_type": "entity",
"text": "Phenotypes for gene: DSCAM were changed from to Autism",
"entity_name": "DSCAM",
"entity_type": "gene"
}
]
}