HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220263,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1368",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1366",
"results": [
{
"created": "2021-03-28T20:13:06.845284+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3567",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LARP7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:12:39.315703+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3566",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LARP7: Rating: GREEN; Mode of pathogenicity: None; Publications: 22865833, 21937992, 30006060, 33569879; Phenotypes: Alazami syndrome, MIM# 615071, Microcephalic primordial dwarfism, Alazami type MONDO:0014031; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:11:15.144043+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6953",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LARP7 as ready",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:11:15.133179+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6953",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: larp7 has been classified as Green List (High Evidence).",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:10:54.394597+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6953",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LARP7 were changed from to Alazami syndrome, MIM# 615071; Microcephalic primordial dwarfism, Alazami type MONDO:0014031",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:10:19.194093+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LARP7 as ready",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:10:19.183234+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: larp7 has been classified as Green List (High Evidence).",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:10:12.176884+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6952",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LARP7 were set to ",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:10:10.672517+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LARP7 were changed from to Alazami syndrome, MIM# 615071; Microcephalic primordial dwarfism, Alazami type MONDO:0014031",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:09:27.830377+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6951",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LARP7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:09:15.158174+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.564",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LARP7 were set to ",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:09:03.020356+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LARP7: Rating: GREEN; Mode of pathogenicity: None; Publications: 22865833, 21937992, 30006060, 33569879; Phenotypes: Alazami syndrome, MIM# 615071, Microcephalic primordial dwarfism, Alazami type MONDO:0014031; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:08:41.280316+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.563",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LARP7 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:08:26.978110+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.563",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LARP7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T20:07:52.147590+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LARP7: Rating: GREEN; Mode of pathogenicity: None; Publications: 22865833, 21937992, 30006060, 33569879; Phenotypes: Alazami syndrome, MIM# 615071, Microcephalic primordial dwarfism, Alazami type MONDO:0014031; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARP7",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:58:23.808274+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3566",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KNL1 as ready",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:58:23.798607+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3566",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: knl1 has been classified as Green List (High Evidence).",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:58:19.923608+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3566",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KNL1 were changed from to Microcephaly 4, primary, autosomal recessive, MIM# 604321; MONDO:0011437",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:57:53.620084+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KNL1 were set to ",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:57:28.341033+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3564",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KNL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:57:00.640904+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3563",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KNL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22983954, 26626498, 27149178, 30304678, 27784895; Phenotypes: Microcephaly 4, primary, autosomal recessive, MIM# 604321, MONDO:0011437; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:56:51.272086+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KNL1 as ready",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:56:51.261367+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: knl1 has been classified as Green List (High Evidence).",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:56:16.660662+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KNL1 as ready",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:56:16.648680+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: knl1 has been classified as Green List (High Evidence).",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:56:08.864623+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KNL1 were changed from to Microcephaly 4, primary, autosomal recessive, MIM# 604321; MONDO:0011437",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:55:51.088962+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KNL1 were set to ",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:55:31.255081+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6948",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KNL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:55:20.072924+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KNL1 were changed from to Microcephaly 4, primary, autosomal recessive, MIM# 604321; MONDO:0011437",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:55:07.680163+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KNL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22983954, 26626498, 27149178, 30304678, 27784895; Phenotypes: Microcephaly 4, primary, autosomal recessive, MIM# 604321, MONDO:0011437; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:54:32.799024+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.561",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KNL1 were set to ",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:54:09.053232+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.560",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KNL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:53:45.072035+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: KNL1: Changed phenotypes: Microcephaly 4, primary, autosomal recessive, MIM# 604321, MONDO:0011437",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:53:24.203738+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KNL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22983954, 26626498, 27149178, 30304678, 27784895; Phenotypes: Microcephaly 4, primary, autosomal recessive, MIM# 604321; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KNL1",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:48:31.052027+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNRC6B were changed from Global developmental delay; Intellectual disability; Autistic behavior to Global developmental delay with speech and behavioural abnormalities, MIM# 619243",
"entity_name": "TNRC6B",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:48:05.734489+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TNRC6B: Changed phenotypes: Global developmental delay with speech and behavioural abnormalities, MIM# 619243",
"entity_name": "TNRC6B",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:47:55.322747+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNRC6B were changed from Global developmental delay; Intellectual disability; Autistic behavior to Global developmental delay with speech and behavioural abnormalities, MIM# 619243",
"entity_name": "TNRC6B",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:47:35.454395+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TNRC6B: Changed phenotypes: Global developmental delay with speech and behavioural abnormalities, MIM# 619243",
"entity_name": "TNRC6B",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:47:32.425290+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3563",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNRC6B were changed from Global developmental delay; Intellectual disability; Autistic behavior to Global developmental delay with speech and behavioural abnormalities, MIM# 619243",
"entity_name": "TNRC6B",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:46:48.980277+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TNRC6B: Changed rating: GREEN; Changed phenotypes: Global developmental delay with speech and behavioural abnormalities, MIM# 619243; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNRC6B",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:45:19.531854+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BAAT as ready",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:45:19.522322+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: baat has been classified as Green List (High Evidence).",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:45:12.532552+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BAAT were changed from to Bile acid conjugation defect 1, MIM# 619232",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:44:53.711599+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6945",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BAAT were set to ",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:44:33.348244+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6944",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BAAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:44:15.745868+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BAAT: Rating: GREEN; Mode of pathogenicity: None; Publications: 12704386, 23415802; Phenotypes: Bile acid conjugation defect 1, MIM# 619232; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:44:07.167882+11:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BAAT were changed from to Bile acid conjugation defect 1, MIM# 619232",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:43:43.386411+11:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BAAT were set to ",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:38:16.198382+11:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BAAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:37:46.443347+11:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BAAT: Rating: GREEN; Mode of pathogenicity: None; Publications: 12704386, 23415802; Phenotypes: Bile acid conjugation defect 1, MIM# 619232; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:36:54.995058+11:00",
"panel_name": "Miscellaneous Metabolic Disorders",
"panel_id": 3468,
"panel_version": "1.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BAAT were changed from Hypercholanemia, familial MIM#607748; disorder of bile acid metabolism to Bile acid conjugation defect 1, MIM# 619232; Hypercholanemia, familial MIM#607748; disorder of bile acid metabolism",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T19:36:14.246513+11:00",
"panel_name": "Miscellaneous Metabolic Disorders",
"panel_id": 3468,
"panel_version": "1.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BAAT: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Bile acid conjugation defect 1, MIM# 619232; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BAAT",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:07:31.812091+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF11 as ready",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:07:31.798882+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif11 has been classified as Green List (High Evidence).",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:07:29.929938+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF11 were changed from Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation, MIM#152950 to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:07:18.353314+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF11 were set to ",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:07:06.616925+11:00",
"panel_name": "Syndromic Retinopathy",
"panel_id": 3099,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:06:26.650729+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF11 were changed from Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918 to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:06:03.085427+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3561",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF11 were changed from Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation MIM#152950 to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:04:51.642382+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3560",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF11 were set to 24281367",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:04:01.768682+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:03:49.743377+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF11 as ready",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:03:49.734240+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif11 has been classified as Green List (High Evidence).",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:03:11.941713+11:00",
"panel_name": "Lymphoedema_syndromic",
"panel_id": 3098,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF11 as ready",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:03:11.931807+11:00",
"panel_name": "Lymphoedema_syndromic",
"panel_id": 3098,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif11 has been classified as Green List (High Evidence).",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:03:09.363913+11:00",
"panel_name": "Lymphoedema_syndromic",
"panel_id": 3098,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF11 were changed from Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation, MCLMR 152950 to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:02:58.851967+11:00",
"panel_name": "Lymphoedema_syndromic",
"panel_id": 3098,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF11 were set to 22284827",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T18:02:45.128825+11:00",
"panel_name": "Lymphoedema_syndromic",
"panel_id": 3098,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:59:47.304089+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF11 were changed from to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:58:10.204771+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF11 as ready",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:58:10.193939+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif11 has been classified as Red List (Low Evidence).",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:58:07.268488+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF11 were changed from to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:57:38.469527+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:57:16.635696+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIF11 as Red List (low evidence)",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:57:16.622311+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif11 has been classified as Red List (Low Evidence).",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:56:47.032161+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:55:37.485405+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF11 as ready",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:55:37.475431+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif11 has been classified as Green List (High Evidence).",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:55:30.818570+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF11 were changed from to Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950; MONDO:0007918",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:55:14.009717+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6942",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF11 were set to ",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:54:56.638575+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6941",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:54:40.159068+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:54:31.497275+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.558",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF11 were set to ",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:53:51.555181+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.557",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:53:48.272278+11:00",
"panel_name": "Monogenic Diabetes",
"panel_id": 3093,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IER3IP1 as ready",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:53:48.261956+11:00",
"panel_name": "Monogenic Diabetes",
"panel_id": 3093,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ier3ip1 has been classified as Green List (High Evidence).",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:53:46.040122+11:00",
"panel_name": "Monogenic Diabetes",
"panel_id": 3093,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IER3IP1 were changed from Microcephaly, epilepsy, and diabetes syndrome to Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231; Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:53:20.120577+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.556",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827, 25115524, 25124931, 27212378, 32730767, 31993640, 25996076; Phenotypes: Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation, MIM# 152950, MONDO:0007918; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:48:08.181033+11:00",
"panel_name": "Monogenic Diabetes",
"panel_id": 3093,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IER3IP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 21835305, 22991235, 24138066, 28711742; Phenotypes: Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231, Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:47:34.995219+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IER3IP1 as ready",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:47:34.985125+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ier3ip1 has been classified as Green List (High Evidence).",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:47:30.833018+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IER3IP1 were changed from to Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231; Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:47:03.960992+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3558",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IER3IP1 were set to ",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:46:42.951282+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3557",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IER3IP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:46:09.307252+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3556",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IER3IP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 21835305, 22991235, 24138066, 28711742; Phenotypes: Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231, Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:45:39.886149+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IER3IP1 as ready",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:45:39.875578+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ier3ip1 has been classified as Green List (High Evidence).",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:45:37.083684+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IER3IP1 were changed from to Microcephaly, epilepsy, and diabetes syndrome, MIM# 614231; Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome, MONDO:0013647",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:45:06.421464+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IER3IP1 were set to ",
"entity_name": "IER3IP1",
"entity_type": "gene"
},
{
"created": "2021-03-28T17:44:48.197165+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IER3IP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IER3IP1",
"entity_type": "gene"
}
]
}