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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2080",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2078",
"results": [
{
"created": "2019-11-30T15:02:43.471741+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DISP1 as ready",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T15:02:43.464592+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: disp1 has been classified as Red List (Low Evidence).",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T15:02:38.775826+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DISP1 were changed from to Holoprosencephaly",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T15:02:26.170614+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DISP1 were set to ",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T15:02:11.319655+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DISP1 as Red List (low evidence)",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T15:02:11.311957+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: disp1 has been classified as Red List (Low Evidence).",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T15:01:58.886288+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DISP1: Rating: RED; Mode of pathogenicity: None; Publications: 19184110, 26748417, 23542665; Phenotypes: Holoprosencephaly; Mode of inheritance: Other",
"entity_name": "DISP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:55:25.499899+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDX59 as ready",
"entity_name": "DDX59",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:55:25.492666+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddx59 has been classified as Green List (High Evidence).",
"entity_name": "DDX59",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:55:21.133150+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDX59 were changed from to Orofaciodigital syndrome V, MIM#174300",
"entity_name": "DDX59",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:55:08.243245+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DDX59 were set to ",
"entity_name": "DDX59",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:54:51.308005+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: DDX59: Some affected individuals are reported as having ID.",
"entity_name": "DDX59",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:51:25.536799+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DDX59: Rating: GREEN; Mode of pathogenicity: None; Publications: 28711741, 23972372, 29127725; Phenotypes: Orofaciodigital syndrome V, MIM#174300; Mode of inheritance: None",
"entity_name": "DDX59",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:47:18.594665+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDR2 as ready",
"entity_name": "DDR2",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:47:18.587035+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddr2 has been classified as Red List (Low Evidence).",
"entity_name": "DDR2",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:47:12.662806+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDR2 were changed from to Warburg-Cinotti syndrome, MIM#618175, AD; Spondylometaepiphyseal dysplasia, short limb-hand type, MIM#271665, AR",
"entity_name": "DDR2",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:46:57.947584+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DDR2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "DDR2",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:46:50.952842+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DDR2 as Red List (low evidence)",
"entity_name": "DDR2",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:46:50.945280+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddr2 has been classified as Red List (Low Evidence).",
"entity_name": "DDR2",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:46:37.160233+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DDR2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Warburg-Cinotti syndrome, MIM#618175, AD, Spondylometaepiphyseal dysplasia, short limb-hand type, MIM#271665, AR; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "DDR2",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:42:42.651713+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDB1 as ready",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:42:42.644540+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddb1 has been classified as Green List (High Evidence).",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:42:37.092788+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DDB1 as Green List (high evidence)",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:42:37.085708+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddb1 has been classified as Green List (High Evidence).",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:42:24.379750+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DDB1 was added\ngene: DDB1 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Research\nMode of inheritance for gene: DDB1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: DDB1 were set to Syndromic intellectual disability\nReview for gene: DDB1 was set to GREEN\nAdded comment: High quality unpublished evidence. \nSources: Research",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:40:44.442988+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DDB1 as ready",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:40:44.435460+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ddb1 has been classified as Green List (High Evidence).",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:40:31.884370+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DDB1 were changed from to Syndromic intellectual disability",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:40:17.347553+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DDB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:39:57.393054+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DDB1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Syndromic intellectual disability; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DDB1",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:34:57.398027+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CNTN4 as ready",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:34:57.390002+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cntn4 has been classified as Red List (Low Evidence).",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:34:51.358677+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CNTN4 were changed from to Intellectual disability; SCA",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:34:38.094162+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CNTN4 were set to ",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:34:20.751704+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CNTN4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:34:14.073958+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CNTN4 as Red List (low evidence)",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2019-11-30T14:34:14.063536+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cntn4 has been classified as Red List (Low Evidence).",
"entity_name": "CNTN4",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:59:03.740220+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP2U1 as ready",
"entity_name": "CYP2U1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:59:03.733050+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp2u1 has been classified as Red List (Low Evidence).",
"entity_name": "CYP2U1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:58:56.411569+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP2U1 were changed from to Spastic paraplegia 56, autosomal recessive, MIM#615030",
"entity_name": "CYP2U1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:58:49.284604+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP2U1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP2U1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:58:32.871180+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CYP2U1 as Red List (low evidence)",
"entity_name": "CYP2U1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:58:32.862771+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp2u1 has been classified as Red List (Low Evidence).",
"entity_name": "CYP2U1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:58:18.744579+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYP2U1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Spastic paraplegia 56, autosomal recessive, MIM#615030; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYP2U1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:01:32.659611+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYFIP1 as ready",
"entity_name": "CYFIP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:01:32.652459+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyfip1 has been classified as Red List (Low Evidence).",
"entity_name": "CYFIP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:01:25.059034+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CYFIP1 as Red List (low evidence)",
"entity_name": "CYFIP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:01:25.051166+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyfip1 has been classified as Red List (Low Evidence).",
"entity_name": "CYFIP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T12:01:09.875513+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYFIP1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "CYFIP1",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:56:00.947891+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CUX2 as ready",
"entity_name": "CUX2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:56:00.938970+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cux2 has been classified as Green List (High Evidence).",
"entity_name": "CUX2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:55:39.792141+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CUX2 were changed from to Epileptic encephalopathy, early infantile, 67, MIM#618141",
"entity_name": "CUX2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:55:17.397850+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CUX2 were set to ",
"entity_name": "CUX2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:54:32.979086+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CUX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CUX2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:53:24.749104+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CUX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 29630738, 29795476; Phenotypes: Epileptic encephalopathy, early infantile, 67, MIM#618141; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CUX2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:50:43.441124+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CUBN as ready",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:50:43.433204+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cubn has been classified as Red List (Low Evidence).",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:50:37.016387+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CUBN were changed from to Megaloblastic anemia-1, Finnish type, MIM#261100; Proteinuria",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:50:18.398213+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CUBN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:50:00.125785+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CUBN as Red List (low evidence)",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:50:00.117610+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cubn has been classified as Red List (Low Evidence).",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:49:48.136916+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CUBN: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Megaloblastic anemia-1, Finnish type, MIM#261100, Proteinuria; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:47:43.342355+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTU2 as ready",
"entity_name": "CTU2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:47:43.334719+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctu2 has been classified as Green List (High Evidence).",
"entity_name": "CTU2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:47:34.385752+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CTU2 as Green List (high evidence)",
"entity_name": "CTU2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:47:34.378296+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctu2 has been classified as Green List (High Evidence).",
"entity_name": "CTU2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:47:19.029780+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CTU2 was added\ngene: CTU2 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: CTU2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CTU2 were set to 27480277; 26633546\nPhenotypes for gene: CTU2 were set to Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome, MIM#618142\nReview for gene: CTU2 was set to GREEN\nAdded comment: Multiple Saudi families reported with same homozygous variant; founder effect. Severe disorder of infancy. \nSources: Expert list",
"entity_name": "CTU2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:41:00.302153+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTSF as ready",
"entity_name": "CTSF",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:41:00.294621+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctsf has been classified as Red List (Low Evidence).",
"entity_name": "CTSF",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:40:44.819596+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTSF were changed from to Ceroid lipofuscinosis, neuronal, 13, Kufs type, MIM#615362",
"entity_name": "CTSF",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:40:37.813613+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CTSF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CTSF",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:40:21.528935+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CTSF as Red List (low evidence)",
"entity_name": "CTSF",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:40:21.520210+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctsf has been classified as Red List (Low Evidence).",
"entity_name": "CTSF",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:40:07.451506+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CTSF: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 13, Kufs type, MIM#615362; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CTSF",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:37:00.552152+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTNNA2 as ready",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:37:00.544298+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctnna2 has been classified as Green List (High Evidence).",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:36:56.236791+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTNNA2 were changed from to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:36:34.421178+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CTNNA2 were set to ",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:36:19.975541+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTNNA2 were changed from Cortical dysplasia, complex, with other brain malformations 9, MIM#618174 to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:36:09.174968+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTNNA2 as ready",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:36:09.166256+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctnna2 has been classified as Green List (High Evidence).",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:36:00.407398+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTNNA2 were changed from Cortical dysplasia, complex, with other brain malformations 9, MIM#618174 to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:35:42.879593+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTNNA2 were changed from to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:35:27.458863+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CTNNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:35:08.264504+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CTNNA2 were set to ",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:34:34.970665+11:00",
"panel_name": "Microcephaly_VCGS",
"panel_id": 138,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CTNNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:34:34.627373+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTNNA2 as ready",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:34:34.603588+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctnna2 has been classified as Green List (High Evidence).",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:33:59.979991+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTNNA2 were changed from to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:33:44.373160+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CTNNA2 were set to ",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:33:27.942969+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CTNNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:29:28.308028+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTNNA2 as ready",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:29:28.300883+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctnna2 has been classified as Green List (High Evidence).",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:29:22.081459+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTNNA2 were changed from to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:29:02.131603+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CTNNA2 were set to ",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:28:35.351367+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CTNNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:28:07.958975+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CTNNA2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30013181; Phenotypes: Cortical dysplasia, complex, with other brain malformations 9, MIM#618174; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:26:15.599274+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTNNA2 as ready",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:26:15.584624+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctnna2 has been classified as Green List (High Evidence).",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:26:14.934069+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CTNNA2 as Green List (high evidence)",
"entity_name": "CTNNA2",
"entity_type": "gene"
}
]
}