HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220504,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2027",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2025",
"results": [
{
"created": "2019-12-27T14:58:32.937780+11:00",
"panel_name": "Ataxia - paediatric_RMH",
"panel_id": 271,
"panel_version": "0.3",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: ACBD5 as ready",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2019-12-27T14:58:32.925505+11:00",
"panel_name": "Ataxia - paediatric_RMH",
"panel_id": 271,
"panel_version": "0.3",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: acbd5 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2019-12-27T14:58:25.090476+11:00",
"panel_name": "Ataxia - paediatric_RMH",
"panel_id": 271,
"panel_version": "0.3",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: ACBD5 as Amber List (moderate evidence)",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2019-12-27T14:58:25.079748+11:00",
"panel_name": "Ataxia - paediatric_RMH",
"panel_id": 271,
"panel_version": "0.3",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: acbd5 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2019-12-27T14:57:49.403141+11:00",
"panel_name": "Ataxia - paediatric_RMH",
"panel_id": 271,
"panel_version": "0.2",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: ACBD5 as Red List (low evidence)",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2019-12-27T14:57:49.392427+11:00",
"panel_name": "Ataxia - paediatric_RMH",
"panel_id": 271,
"panel_version": "0.2",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: acbd5 has been classified as Red List (Low Evidence).",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2019-12-27T14:57:38.207889+11:00",
"panel_name": "Ataxia - paediatric_RMH",
"panel_id": 271,
"panel_version": "0.1",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ACBD5 was added\ngene: ACBD5 was added to Ataxia - paediatric_RMH. Sources: Expert list\nMode of inheritance for gene: ACBD5 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ACBD5 were set to 27799409; 23105016\nPhenotypes for gene: ACBD5 were set to Leukodystrophy; syndromic cleft palate; ataxia; retinal dystrophy\nReview for gene: ACBD5 was set to AMBER\nAdded comment: 2 unrelated families and no functional evidence \nSources: Expert list",
"entity_name": "ACBD5",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:50:55.752068+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MN1 as ready",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:50:55.741161+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mn1 has been classified as Green List (High Evidence).",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:50:41.627260+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MN1 were changed from to Intellectual disability; dysmophic features; rhombencephalosynapsis",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:50:28.229697+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MN1 were set to ",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:50:10.836582+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.420",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: MN1 was changed from to Other",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:49:56.657110+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.419",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MN1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:49:37.336753+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MN1: Rating: GREEN; Mode of pathogenicity: Other; Publications: 31834374, 31839203; Phenotypes: Intellectual disability, dysmophic features, rhombencephalosynapsis; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:47:41.904402+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MN1 as ready",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:47:41.893692+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mn1 has been classified as Green List (High Evidence).",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:47:37.981044+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MN1 as Green List (high evidence)",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:47:37.969935+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mn1 has been classified as Green List (High Evidence).",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:47:22.616988+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MN1 was added\ngene: MN1 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: MN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MN1 were set to 31834374; 31839203\nPhenotypes for gene: MN1 were set to Intellectual disability; dysmophic features; rhombencephalosynapsis\nMode of pathogenicity for gene: MN1 was set to Other\nReview for gene: MN1 was set to GREEN\nAdded comment: Over 20 individuals described with de novo truncating variants in this gene; these cluster in the C-terminal and the authors postulate that that syndrome is not due to MN1 haploinsufficiency but rather is the result of dominantly acting C-terminally truncated MN1 protein. \nSources: Literature",
"entity_name": "MN1",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:38:52.423959+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF8 as ready",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:38:52.413324+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf8 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:38:41.511942+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFAF8 as Green List (high evidence)",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:38:41.501055+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.418",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf8 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:36:35.802373+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.417",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NDUFAF8 was added\ngene: NDUFAF8 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: NDUFAF8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NDUFAF8 were set to 31866046\nPhenotypes for gene: NDUFAF8 were set to Leigh syndrome\nReview for gene: NDUFAF8 was set to GREEN\nAdded comment: Three unrelated individuals with bi-allelic variants in this gene; functional data. Beware recurrent deep intronic splicing variant. \nSources: Literature",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:34:25.169659+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF8 as ready",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:34:25.158860+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf8 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:34:20.397496+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFAF8 as Green List (high evidence)",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:34:20.386401+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf8 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T12:33:50.138907+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NDUFAF8 was added\ngene: NDUFAF8 was added to Mitochondrial_AustralianGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: NDUFAF8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NDUFAF8 were set to 31866046\nPhenotypes for gene: NDUFAF8 were set to Leigh syndrome\nReview for gene: NDUFAF8 was set to GREEN\nAdded comment: Three unrelated individuals with bi-allelic variants in this gene; functional data. Beware recurrent deep intronic splicing variant. \nSources: Literature",
"entity_name": "NDUFAF8",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:39:40.568733+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EEF1B2 as ready",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:39:40.557983+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eef1b2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:39:21.650833+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EEF1B2 as Amber List (moderate evidence)",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:39:21.640179+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eef1b2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:39:03.764576+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.415",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: EEF1B2 was added\ngene: EEF1B2 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: EEF1B2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: EEF1B2 were set to 31845318; 21937992\nPhenotypes for gene: EEF1B2 were set to Intellectual disability\nReview for gene: EEF1B2 was set to AMBER\nAdded comment: 5 individuals from two unrelated families described in the literature so far, no functional data but gene belongs to a family implicated in neurodevelopmental disorders. \nSources: Literature",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:36:43.839478+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EEF1B2 as ready",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:36:43.828696+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eef1b2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:36:37.449796+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EEF1B2 as Amber List (moderate evidence)",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:36:37.437563+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eef1b2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-27T09:36:24.640689+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: EEF1B2 was added\ngene: EEF1B2 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: EEF1B2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: EEF1B2 were set to 31845318; 21937992\nPhenotypes for gene: EEF1B2 were set to Intellectual disability\nReview for gene: EEF1B2 was set to AMBER\nAdded comment: 5 individuals from two unrelated families described in the literature so far, no functional data but gene belongs to a family implicated in neurodevelopmental disorders. \nSources: Literature",
"entity_name": "EEF1B2",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.772118+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: TRPM1 was added\ngene: TRPM1 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TRPM1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TRPM1 were set to Night blindness, congenital stationary (complete), 1C, autosomal recessive, 613216",
"entity_name": "TRPM1",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.705850+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: SLC24A1 was added\ngene: SLC24A1 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SLC24A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: SLC24A1 were set to Night blindness, congenital stationary (complete), 1D, autosomal recessive, 613830",
"entity_name": "SLC24A1",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.640614+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: SAG was added\ngene: SAG was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SAG was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: SAG were set to Oguchi Disease; Retinitis pigmentosa 47; Congenital Stationary Night Blindness",
"entity_name": "SAG",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.574690+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: RPE65 was added\ngene: RPE65 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RPE65 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RPE65 were set to Retinitis pigmentosa 20; Leber congenital amaurosis 2, 204100; Leber Congenital Amaurosis; Leber congenital amaurosis 2",
"entity_name": "RPE65",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.510713+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: RHO was added\ngene: RHO was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RHO was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RHO were set to Retinitis punctata albescens; Retinitis pigmentosa; Night blindness, congenital stationary autosomal dominant 1",
"entity_name": "RHO",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.444418+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: RDH5 was added\ngene: RDH5 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RDH5 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RDH5 were set to Achromatopsia, Cone, and Cone-rod Dystrophy; Fundus albipunctatus, 136880; Fundus albipunctatus; Congenital Stationary Night Blindness",
"entity_name": "RDH5",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.379818+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: PDE6B was added\ngene: PDE6B was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PDE6B was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: PDE6B were set to Night blindness, congenital stationary, autosomal dominant 2, 163500; Retinitis pigmentosa",
"entity_name": "PDE6B",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.312457+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: NYX was added\ngene: NYX was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: NYX was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: NYX were set to Night blindness, congenital stationary (complete), 1A, X-linked, 310500",
"entity_name": "NYX",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.248685+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: LRIT3 was added\ngene: LRIT3 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: LRIT3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LRIT3 were set to Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058",
"entity_name": "LRIT3",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.184123+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GRM6 was added\ngene: GRM6 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GRM6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GRM6 were set to Night blindness, congenital stationary (complete), 1B, autosomal recessive, 257270",
"entity_name": "GRM6",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:40.119310+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GRK1 was added\ngene: GRK1 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GRK1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GRK1 were set to Oguchi disease-2, 613411",
"entity_name": "GRK1",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:39.955415+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GPR179 was added\ngene: GPR179 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GPR179 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GPR179 were set to Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565",
"entity_name": "GPR179",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:39.888824+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GNB3 was added\ngene: GNB3 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GNB3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GNB3 were set to Night blindness, congenital stationary, type 1h",
"entity_name": "GNB3",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:39.810716+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: GNAT1 was added\ngene: GNAT1 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GNAT1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: GNAT1 were set to Night blindness, congenital stationary, autosomal dominant 3, 610444",
"entity_name": "GNAT1",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:39.747320+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CHM was added\ngene: CHM was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CHM was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPhenotypes for gene: CHM were set to Choroideremia (degeneration of the choriocapillaris, the retinal pigment epithelium, and the photoreceptor of the eye)",
"entity_name": "CHM",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:39.682123+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CACNA2D4 was added\ngene: CACNA2D4 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CACNA2D4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CACNA2D4 were set to Retinal cone dystrophy 4, 610478; Congenital Stationary Night Blindness",
"entity_name": "CACNA2D4",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:39.619994+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CACNA1F was added\ngene: CACNA1F was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CACNA1F was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPhenotypes for gene: CACNA1F were set to Cone-rod dystropy, X-linked, 3, 300476; Aland Island eye disease, 300600; Night blindness, congenital stationary (incomplete), 2A, X-linked, 300071",
"entity_name": "CACNA1F",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:39.552408+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CABP4 was added\ngene: CABP4 was added to Congenital Stationary Night Blindness_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CABP4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CABP4 were set to Night blindness, congenital stationary (incomplete), 2B, autosomal recessive, 610427",
"entity_name": "CABP4",
"entity_type": "gene"
},
{
"created": "2019-12-24T14:19:39.501115+11:00",
"panel_name": "Congenital Stationary Night Blindness_RMH",
"panel_id": 283,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "panel",
"text": "Added panel Congenital Stationary Night Blindness_RMH",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-24T13:32:00.412435+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC26A4 as ready",
"entity_name": "SLC26A4",
"entity_type": "gene"
},
{
"created": "2019-12-24T13:32:00.400548+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc26a4 has been classified as Green List (High Evidence).",
"entity_name": "SLC26A4",
"entity_type": "gene"
},
{
"created": "2019-12-24T13:27:57.474753+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC26A4 were changed from to Deafness, autosomal recessive 4, with enlarged vestibular aqueduct, MIM#600791; Pendred syndrome, MIM#274600",
"entity_name": "SLC26A4",
"entity_type": "gene"
},
{
"created": "2019-12-24T13:27:34.251386+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC26A4 were set to ",
"entity_name": "SLC26A4",
"entity_type": "gene"
},
{
"created": "2019-12-24T13:27:12.339228+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC26A4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC26A4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:41:03.866771+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.8",
"user_name": "Chern Lim",
"item_type": "entity",
"text": "reviewed gene: SLC26A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 9618167, 19204907; Phenotypes: Deafness, autosomal recessive 4, with enlarged vestibular aqueduct, MIM#600791, Pendred syndrome, MIM#274600; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC26A4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:39:49.018687+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.8",
"user_name": "Chern Lim",
"item_type": "entity",
"text": "Deleted their review",
"entity_name": "SLC26A4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:39:17.874808+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.8",
"user_name": "Chern Lim",
"item_type": "entity",
"text": "reviewed gene: SLC26A4: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 9618167, 19204907; Phenotypes: Deafness, autosomal recessive 4, with enlarged vestibular aqueduct, MIM#600791, Pendred syndrome, MIM#274600; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC26A4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:20:18.371905+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: YAP1 as ready",
"entity_name": "YAP1",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:20:18.360104+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: yap1 has been classified as Green List (High Evidence).",
"entity_name": "YAP1",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:20:14.856400+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: YAP1 as Green List (high evidence)",
"entity_name": "YAP1",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:20:14.845162+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: yap1 has been classified as Green List (High Evidence).",
"entity_name": "YAP1",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:19:45.684241+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: YAP1 was added\ngene: YAP1 was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: YAP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: YAP1 were set to Coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation, MIM#120433\nReview for gene: YAP1 was set to GREEN\nAdded comment: Coloboma is part of the phenotype. \nSources: Expert list",
"entity_name": "YAP1",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:18:07.826050+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SMO as ready",
"entity_name": "SMO",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:18:07.813985+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: smo has been classified as Green List (High Evidence).",
"entity_name": "SMO",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:18:04.618675+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SMO as Green List (high evidence)",
"entity_name": "SMO",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:18:04.607442+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: smo has been classified as Green List (High Evidence).",
"entity_name": "SMO",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:17:36.531046+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SMO was added\ngene: SMO was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: SMO was set to Other\nPhenotypes for gene: SMO were set to Curry-Jones syndrome, somatic mosaic, MIM#601707\nReview for gene: SMO was set to GREEN\nAdded comment: Microphthalmia and coloboma are part of the phenotype of this somatic mosaic condition. \nSources: Expert list",
"entity_name": "SMO",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:15:32.277018+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SALL4 as ready",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:15:32.266356+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sall4 has been classified as Green List (High Evidence).",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:15:28.622938+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SALL4 as Green List (high evidence)",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:15:28.612051+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sall4 has been classified as Green List (High Evidence).",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:14:59.827257+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SALL4 was added\ngene: SALL4 was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: SALL4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SALL4 were set to Duane-radial ray syndrome, MIM#607323\nReview for gene: SALL4 was set to GREEN\nAdded comment: Microphthalmia and coloboma are part of the phenotype. \nSources: Expert list",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:12:38.770599+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPGRIP1L as ready",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:12:38.759491+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rpgrip1l has been classified as Green List (High Evidence).",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:12:35.369392+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RPGRIP1L as Green List (high evidence)",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:12:35.358584+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rpgrip1l has been classified as Green List (High Evidence).",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:12:07.882079+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RPGRIP1L was added\ngene: RPGRIP1L was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: RPGRIP1L was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RPGRIP1L were set to COACH syndrome, MIM#216360\nReview for gene: RPGRIP1L was set to GREEN\nAdded comment: Coloboma is part of the phenotype. \nSources: Expert list",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:10:29.682796+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PUF60 as ready",
"entity_name": "PUF60",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:10:29.669460+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: puf60 has been classified as Green List (High Evidence).",
"entity_name": "PUF60",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:10:25.679129+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PUF60 as Green List (high evidence)",
"entity_name": "PUF60",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:10:25.668604+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: puf60 has been classified as Green List (High Evidence).",
"entity_name": "PUF60",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:09:57.620523+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PUF60 was added\ngene: PUF60 was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: PUF60 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PUF60 were set to Verheij syndrome, MIM#615583\nReview for gene: PUF60 was set to GREEN\nAdded comment: Coloboma is part of the phenotype. \nSources: Expert list",
"entity_name": "PUF60",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:08:07.776903+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PORCN as ready",
"entity_name": "PORCN",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:08:07.763306+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: porcn has been classified as Green List (High Evidence).",
"entity_name": "PORCN",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:08:02.474888+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PORCN as Green List (high evidence)",
"entity_name": "PORCN",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:08:02.463772+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: porcn has been classified as Green List (High Evidence).",
"entity_name": "PORCN",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:07:33.799134+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PORCN was added\ngene: PORCN was added to Anophthalmia, microphthalmia, coloboma_VCGS. Sources: Expert list\nMode of inheritance for gene: PORCN was set to Other\nPhenotypes for gene: PORCN were set to Focal dermal hypoplasia, MIM#305600\nReview for gene: PORCN was set to GREEN\nAdded comment: Anophthalmia, microphthalmia and coloboma are part of the phenotype of this XLD condition. \nSources: Expert list",
"entity_name": "PORCN",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:05:26.035755+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LRP2 as ready",
"entity_name": "LRP2",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:05:25.994349+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lrp2 has been classified as Green List (High Evidence).",
"entity_name": "LRP2",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:05:20.736411+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LRP2 as Green List (high evidence)",
"entity_name": "LRP2",
"entity_type": "gene"
},
{
"created": "2019-12-24T11:05:20.725456+11:00",
"panel_name": "Anophthalmia, microphthalmia, coloboma_VCGS",
"panel_id": 42,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lrp2 has been classified as Green List (High Evidence).",
"entity_name": "LRP2",
"entity_type": "gene"
}
]
}