HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220314,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1448",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1446",
"results": [
{
"created": "2021-01-06T21:46:24.590108+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VCAN were changed from to Wagner syndrome 1, MIM# 143200",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:46:02.354272+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6001",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VCAN were set to ",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:45:42.601717+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.6000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: VCAN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:45:15.061485+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: VCAN: Rating: GREEN; Mode of pathogenicity: None; Publications: 16877430, 22739342, 16636652, 16043844, 32854301, 30657523, 30055036, 29071374, 27667122; Phenotypes: Wagner syndrome 1, MIM# 143200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:44:22.599876+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VCAN as ready",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:44:22.587856+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vcan has been classified as Green List (High Evidence).",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:44:20.213598+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VCAN were changed from to Wagner syndrome 1, MIM# 143200",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:44:12.553004+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VCAN were set to ",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:44:03.838448+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: VCAN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:43:55.772957+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: VCAN.",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:43:48.405778+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: VCAN: Rating: GREEN; Mode of pathogenicity: None; Publications: 16877430, 22739342, 16636652, 16043844, 32854301, 30657523, 30055036, 29071374, 27667122; Phenotypes: Wagner syndrome 1, MIM# 143200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "VCAN",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:40:38.449682+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF408 as ready",
"entity_name": "ZNF408",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:40:38.434897+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf408 has been classified as Green List (High Evidence).",
"entity_name": "ZNF408",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:40:36.035671+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF408 were changed from to Exudative vitreoretinopathy 6, MIM# 616468",
"entity_name": "ZNF408",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:40:23.489651+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF408 were set to ",
"entity_name": "ZNF408",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:39:52.426849+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZNF408 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZNF408",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:39:41.275298+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZNF408: Rating: GREEN; Mode of pathogenicity: None; Publications: 23716654, 32530348, 32097476, 32238352, 30998249, 29982478; Phenotypes: Exudative vitreoretinopathy 6, MIM# 616468; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZNF408",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:36:30.159250+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CAPN5 as ready",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:36:30.148005+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: capn5 has been classified as Green List (High Evidence).",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:34:53.310600+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CAPN5 were changed from to Vitreoretinopathy, neovascular inflammatory, MIM# 193235",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:34:31.039811+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5998",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CAPN5 were set to ",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:34:11.264969+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5997",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CAPN5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:33:48.940813+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CAPN5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23055945, 32274441, 31110225, 30986125; Phenotypes: Vitreoretinopathy, neovascular inflammatory, MIM# 193235; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:33:04.137347+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CAPN5 as ready",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:33:04.129068+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: capn5 has been classified as Green List (High Evidence).",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:33:01.732771+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CAPN5 were changed from to Vitreoretinopathy, neovascular inflammatory, MIM# 193235",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:32:53.964992+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CAPN5 were set to ",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:32:45.744725+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CAPN5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T21:32:34.382112+11:00",
"panel_name": "Vitreoretinopathy",
"panel_id": 3113,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CAPN5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23055945, 32274441, 31110225, 30986125; Phenotypes: Vitreoretinopathy, neovascular inflammatory, MIM# 193235; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CAPN5",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:32:12.874414+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2021-01-06T14:31:56.863179+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBIAD1 as ready",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:31:56.855637+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ubiad1 has been classified as Green List (High Evidence).",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:31:55.525443+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBIAD1 were changed from Corneal dystrophy, Schnyder type, MIM# 121800 to Corneal dystrophy, Schnyder type, MIM# 121800",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:31:35.313535+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBIAD1 as ready",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:31:35.301816+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ubiad1 has been classified as Green List (High Evidence).",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:31:31.007710+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBIAD1 were changed from to Corneal dystrophy, Schnyder type, MIM# 121800",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:31:25.565544+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBIAD1 were changed from to Corneal dystrophy, Schnyder type, MIM# 121800",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:30:50.349911+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5995",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBIAD1 were set to ",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:30:32.013673+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5994",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UBIAD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:30:13.538887+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UBIAD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18176953, 23169578, 31323021, 30785396, 30223810; Phenotypes: Corneal dystrophy, Schnyder type, MIM# 121800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:30:10.971754+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBIAD1 were set to ",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:29:42.871832+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UBIAD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:29:07.968453+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UBIAD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18176953, 23169578, 31323021, 30785396, 30223810; Phenotypes: Corneal dystrophy, Schnyder type, MIM# 121800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "UBIAD1",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:26:52.313043+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TGFBI as ready",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:26:52.304589+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tgfbi has been classified as Green List (High Evidence).",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:26:44.070450+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TGFBI as ready",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:26:44.058748+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tgfbi has been classified as Green List (High Evidence).",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:26:43.295903+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TGFBI were changed from to Corneal dystrophy, multiple types, MONDO:0000764",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:26:26.652850+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TGFBI were changed from to Corneal dystrophy, multiple types, MONDO:0000764",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:26:22.797004+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5992",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TGFBI were set to ",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:26:03.999716+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5991",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TGFBI was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:25:45.164428+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TGFBI: Rating: GREEN; Mode of pathogenicity: None; Publications: 9054935; Phenotypes: Corneal dystrophy, multiple types, MONDO:0000764; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:25:44.514106+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TGFBI were set to ",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:25:18.612213+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TGFBI was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:24:49.630026+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TGFBI: Rating: GREEN; Mode of pathogenicity: None; Publications: 9054935; Phenotypes: Corneal dystrophy, multiple types, MONDO:0000764; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TGFBI",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:22:28.659837+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCF4 as ready",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:22:28.649395+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcf4 has been classified as Green List (High Evidence).",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:22:26.462668+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCF4 were changed from to Corneal dystrophy, Fuchs endothelial, 3, MIM# 613267",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:22:02.788789+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCF4 were set to ",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:21:32.128934+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TCF4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:21:03.127692+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag STR tag was added to gene: TCF4.",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:20:54.332184+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TCF4: Rating: GREEN; Mode of pathogenicity: Other; Publications: 25722209; Phenotypes: Corneal dystrophy, Fuchs endothelial, 3, MIM# 613267; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:18:46.221626+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TACSTD2 as ready",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:18:46.211905+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tacstd2 has been classified as Green List (High Evidence).",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:18:38.602799+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5990",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TACSTD2 were changed from to Corneal dystrophy, gelatinous drop-like, MIM# 204870",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:18:19.583208+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5989",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TACSTD2 were set to ",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:17:57.916083+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5988",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TACSTD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:17:37.872857+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TACSTD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10192395, 12107443, 12614764, 31666974, 31534795; Phenotypes: Corneal dystrophy, gelatinous drop-like, MIM# 204870; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:17:29.794667+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TACSTD2 as ready",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:17:29.782928+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tacstd2 has been classified as Green List (High Evidence).",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:16:55.434777+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TACSTD2 were changed from to Corneal dystrophy, gelatinous drop-like, MIM# 204870",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:16:29.888881+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TACSTD2 were set to ",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:16:02.248988+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TACSTD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:15:32.475321+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TACSTD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10192395, 12107443, 12614764, 31666974, 31534795; Phenotypes: Corneal dystrophy, gelatinous drop-like, MIM# 204870; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TACSTD2",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:13:06.348883+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC4A11 as ready",
"entity_name": "SLC4A11",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:13:06.336660+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc4a11 has been classified as Green List (High Evidence).",
"entity_name": "SLC4A11",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:13:04.111998+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC4A11 were changed from to Corneal dystrophy, Fuchs endothelial, 4, MIM# 613268; Corneal endothelial dystrophy and perceptive deafness, MIM# 217400; Corneal endothelial dystrophy, autosomal recessive, MIM# 217700",
"entity_name": "SLC4A11",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:12:35.502068+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC4A11 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "SLC4A11",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:12:06.372101+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC4A11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Corneal dystrophy, Fuchs endothelial, 4, MIM# 613268, Corneal endothelial dystrophy and perceptive deafness, MIM# 217400, Corneal endothelial dystrophy, autosomal recessive, MIM# 217700; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "SLC4A11",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:09:09.499201+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRDM5 as ready",
"entity_name": "PRDM5",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:09:09.491087+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prdm5 has been classified as Green List (High Evidence).",
"entity_name": "PRDM5",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:09:06.690094+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRDM5 were changed from to Brittle cornea syndrome 2, MIM# 614170",
"entity_name": "PRDM5",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:08:36.843416+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRDM5 were set to ",
"entity_name": "PRDM5",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:08:06.708011+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRDM5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PRDM5",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:07:37.205717+11:00",
"panel_name": "Corneal Dystrophy",
"panel_id": 91,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRDM5: Rating: GREEN; Mode of pathogenicity: None; Publications: 21664999, 22122778, 26395458, 33120686, 27032025; Phenotypes: Brittle cornea syndrome 2, MIM# 614170; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PRDM5",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:04:47.594552+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF27 as ready",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:04:47.581193+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif27 has been classified as Red List (Low Evidence).",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:04:38.789590+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIF27 as Red List (low evidence)",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:04:38.781179+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5987",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif27 has been classified as Red List (Low Evidence).",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:04:15.793535+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF27 as ready",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:04:15.784639+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif27 has been classified as Red List (Low Evidence).",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:04:12.498730+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIF27 as Red List (low evidence)",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T14:04:12.486844+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif27 has been classified as Red List (Low Evidence).",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T12:08:20.229801+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5986",
"user_name": "Anna Le Fevre",
"item_type": "entity",
"text": "reviewed gene: KIF27: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: Unknown",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T12:07:31.288239+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.244",
"user_name": "Anna Le Fevre",
"item_type": "entity",
"text": "reviewed gene: KIF27: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: Unknown",
"entity_name": "KIF27",
"entity_type": "gene"
},
{
"created": "2021-01-06T11:24:08.783083+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZEB1 as ready",
"entity_name": "ZEB1",
"entity_type": "gene"
},
{
"created": "2021-01-06T11:24:08.772359+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zeb1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZEB1",
"entity_type": "gene"
},
{
"created": "2021-01-06T11:24:06.074206+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZEB1 were changed from to Corneal dystrophy, Fuchs endothelial, 6, MIM# 613270; Corneal dystrophy, posterior polymorphous, 3, MIM# 609141; Corpus callosum abnormalities",
"entity_name": "ZEB1",
"entity_type": "gene"
},
{
"created": "2021-01-06T11:23:38.106431+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZEB1 were set to ",
"entity_name": "ZEB1",
"entity_type": "gene"
},
{
"created": "2021-01-06T11:23:09.306810+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZEB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZEB1",
"entity_type": "gene"
}
]
}