HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220504,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2030",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2028",
"results": [
{
"created": "2019-12-23T15:41:31.481450+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.402",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: REV3L was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "REV3L",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:40:54.141626+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.401",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: REV3L: Rating: GREEN; Mode of pathogenicity: None; Publications: 26068067, 26068067; Phenotypes: Moebius syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "REV3L",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:36:14.301176+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SELP as ready",
"entity_name": "SELP",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:36:14.294493+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: selp has been classified as Red List (Low Evidence).",
"entity_name": "SELP",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:35:49.933233+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SELP as Red List (low evidence)",
"entity_name": "SELP",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:35:49.924913+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.401",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: selp has been classified as Red List (Low Evidence).",
"entity_name": "SELP",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:35:17.257260+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.400",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: SELP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "SELP",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:31:46.931688+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FLG2 as ready",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:31:46.923943+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flg2 has been classified as Green List (High Evidence).",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:31:41.994192+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FLG2 as Green List (high evidence)",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:31:41.986496+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flg2 has been classified as Green List (High Evidence).",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:31:04.105852+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FLG2 as ready",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:31:04.098953+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flg2 has been classified as Green List (High Evidence).",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:30:26.275813+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FLG2 as Green List (high evidence)",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:30:26.268619+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.400",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flg2 has been classified as Green List (High Evidence).",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:30:06.786651+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.399",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FLG2 was added\ngene: FLG2 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: FLG2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FLG2 were set to 29758285; 28884927; 29505760\nPhenotypes for gene: FLG2 were set to Peeling skin syndrome 6, MIM#\t618084\nReview for gene: FLG2 was set to GREEN\nAdded comment: 3 unrelated families reported. \nSources: Literature",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:29:12.380035+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.0",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "gene: FLG2 was added\ngene: FLG2 was added to Epidermolysis bullosa_VCGS. Sources: Literature\nMode of inheritance for gene: FLG2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FLG2 were set to 29758285; 28884927; 29505760\nPhenotypes for gene: FLG2 were set to Peeling skin syndrome 6, MIM#\t618084\nReview for gene: FLG2 was set to GREEN\nAdded comment: 3 unrelated families reported \nSources: Literature",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:28:12.651386+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FLG2 as ready",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:28:12.644655+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flg2 has been classified as Green List (High Evidence).",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:27:59.927921+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FLG2 as Green List (high evidence)",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:27:59.917697+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flg2 has been classified as Green List (High Evidence).",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:26:57.291091+11:00",
"panel_name": "Ichthyosis_VCGS",
"panel_id": 124,
"panel_version": "0.0",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "gene: FLG2 was added\ngene: FLG2 was added to Ichthyosis_VCGS. Sources: Literature\nMode of inheritance for gene: FLG2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FLG2 were set to 29758285; 28884927; 29505760\nPhenotypes for gene: FLG2 were set to Peeling skin syndrome 6, MIM#\t618084\nReview for gene: FLG2 was set to GREEN\nAdded comment: 3 unrelated families reported \nSources: Literature",
"entity_name": "FLG2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:14:01.182481+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NLRP2 as ready",
"entity_name": "NLRP2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:14:01.175360+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nlrp2 has been classified as Green List (High Evidence).",
"entity_name": "NLRP2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:13:53.020578+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.398",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NLRP2 were changed from to female infertility; early embryonic arrest",
"entity_name": "NLRP2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:13:33.311964+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.397",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NLRP2 were set to ",
"entity_name": "NLRP2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:13:19.426790+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.396",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NLRP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NLRP2",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:12:31.616563+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.395",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: NLRP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30877238; Phenotypes: female infertility, early embryonic arrest; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NLRP2",
"entity_type": "gene"
},
{
"created": "2019-12-23T14:39:18.097906+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.13",
"user_name": "chirag patel",
"item_type": "entity",
"text": "changed review comment from: Very few renal cysts seen in patients. If this PLD gene is in the panel, then we should have all the PLD genes, where very occasional renal cysts can be seen.; to: Renal cysts not a key or common feature seen in these patients. If this PLD gene is in the panel, then we should have all the PLD genes, where very occasional renal cysts can be seen.",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-23T14:39:10.612087+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SEC63 as Red List (low evidence)",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-23T14:39:10.607934+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Discussed with Chirag Patel: we should have a consistent approach to all liver cystic disease genes. Renal cysts are not a key feature, therefore Red for this panel.",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-23T14:39:10.589198+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sec63 has been classified as Red List (Low Evidence).",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-23T14:37:28.614637+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.12",
"user_name": "chirag patel",
"item_type": "entity",
"text": "reviewed gene: SEC63: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Polycystic liver disease 2, OMIM #617004; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-23T14:31:26.455727+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.11",
"user_name": "chirag patel",
"item_type": "panel",
"text": "Panel name changed from Renal ciliopathies and nephronophthisis_KidGen to Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-22T18:15:49.888976+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D32 as ready",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:15:49.882114+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d32 has been classified as Red List (Low Evidence).",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:15:45.535748+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBC1D32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:15:21.107695+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D32 were set to ",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:14:59.101174+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D32 were changed from to Orofaciodigital syndrome type IX",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:14:34.218569+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TBC1D32 as Red List (low evidence)",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:14:34.209571+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d32 has been classified as Red List (Low Evidence).",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:14:07.142301+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBC1D32: Rating: RED; Mode of pathogenicity: None; Publications: 24285566; Phenotypes: Orofaciodigital syndrome type IX; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:13:33.721041+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D32 as ready",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:13:33.714219+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d32 has been classified as Red List (Low Evidence).",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:13:23.713710+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D32 were set to ",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:13:09.572166+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D32 were changed from to Orofaciodigital syndrome type IX",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:12:53.682892+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.393",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBC1D32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:12:28.442708+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TBC1D32 as Red List (low evidence)",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:12:28.435795+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d32 has been classified as Red List (Low Evidence).",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:12:06.439756+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBC1D32: Rating: RED; Mode of pathogenicity: None; Publications: 24285566; Phenotypes: Orofaciodigital syndrome type IX; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:11:05.116727+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D32 as ready",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:11:05.109752+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d32 has been classified as Red List (Low Evidence).",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:11:01.717495+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D32 were changed from to Orofaciodigital syndrome type IX",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:10:33.198580+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D32 were set to ",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:10:10.926265+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBC1D32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:09:44.029839+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TBC1D32 as Red List (low evidence)",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:09:44.022476+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d32 has been classified as Red List (Low Evidence).",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:09:16.791148+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBC1D32: Rating: RED; Mode of pathogenicity: None; Publications: 24285566; Phenotypes: Orofaciodigital syndrome type IX; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D32",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:04:16.090647+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SCLT1 as ready",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:04:16.083737+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sclt1 has been classified as Green List (High Evidence).",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:04:11.814984+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SCLT1 were changed from to Orofaciodigital syndrome type IX; Senior-Loken syndrome",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:03:50.687553+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SCLT1 were set to ",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:03:16.289738+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SCLT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:02:48.075821+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SCLT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28486600, 30425282, 30237576, 28005958, 24285566; Phenotypes: Orofaciodigital syndrome type IX, Senior-Loken syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:01:40.651255+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SCLT1 as ready",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:01:40.641440+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sclt1 has been classified as Green List (High Evidence).",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:01:35.208481+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SCLT1 as Green List (high evidence)",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:01:35.201849+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sclt1 has been classified as Green List (High Evidence).",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-22T18:01:22.254447+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SCLT1 was added\ngene: SCLT1 was added to Renal ciliopathies and nephronophthisis_KidGen. Sources: Expert list\nMode of inheritance for gene: SCLT1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SCLT1 were set to 28486600; 30425282; 30237576; 28005958; 24285566\nPhenotypes for gene: SCLT1 were set to Orofaciodigital syndrome type IX; Senior-Loken syndrome\nReview for gene: SCLT1 was set to GREEN\nAdded comment: Reports of individual patients with overlapping features suggestive of ciliopathy, mouse model recapitulates phenotype. \nSources: Expert list",
"entity_name": "SCLT1",
"entity_type": "gene"
},
{
"created": "2019-12-21T18:27:35.703359+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SEC63 as ready",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-21T18:27:35.696736+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sec63 has been classified as Green List (High Evidence).",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-21T18:27:30.191534+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SEC63 as Green List (high evidence)",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-21T18:27:30.184778+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sec63 has been classified as Green List (High Evidence).",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-21T18:27:19.228943+11:00",
"panel_name": "Renal macrocystic disease_KidGen_VCGS",
"panel_id": 194,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SEC63 was added\ngene: SEC63 was added to Renal macrocystic disease_KidGen_VCGS. Sources: Expert list\nMode of inheritance for gene: SEC63 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SEC63 were set to 15133510\nPhenotypes for gene: SEC63 were set to Polycystic liver disease 2, MIM#617004\nReview for gene: SEC63 was set to GREEN\nAdded comment: Renal cysts reported in some individuals; no significant renal impairment. \nSources: Expert list",
"entity_name": "SEC63",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:33:46.180447+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EXOC3L2 as ready",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:33:46.172903+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: exoc3l2 has been classified as Green List (High Evidence).",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:33:35.364202+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EXOC3L2 were changed from to Dandy-Walker malformation; renal dysplasia; bone marrow failure",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:33:18.308488+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.390",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EXOC3L2 were set to ",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:32:58.167867+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EXOC3L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:32:40.658456+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EXOC3L2 were changed from Dandy-Walker malformation; renal dysplasia; bone marrow failure to Dandy-Walker malformation; renal dysplasia; bone marrow failure",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:32:23.980941+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EXOC3L2 as ready",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:32:23.972898+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: exoc3l2 has been classified as Green List (High Evidence).",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:32:19.319675+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EXOC3L2 were changed from to Dandy-Walker malformation; renal dysplasia; bone marrow failure",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:31:55.723740+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EXOC3L2 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:31:05.996673+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EXOC3L2 were set to ",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:30:48.335381+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EXOC3L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:29:44.126080+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EXOC3L2 as ready",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:29:44.118097+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: exoc3l2 has been classified as Green List (High Evidence).",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:29:35.575569+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EXOC3L2 as Green List (high evidence)",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:29:35.568614+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: exoc3l2 has been classified as Green List (High Evidence).",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-21T17:29:08.353470+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: EXOC3L2 was added\ngene: EXOC3L2 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Literature\nMode of inheritance for gene: EXOC3L2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: EXOC3L2 were set to 30327448; 28749478; 27894351\nPhenotypes for gene: EXOC3L2 were set to Dandy-Walker malformation; renal dysplasia; bone marrow failure\nReview for gene: EXOC3L2 was set to GREEN\nAdded comment: Four individuals from two unrelated families with brain, kidney and bone marrow abnormalities; another described as part of fetal autopsy series, and another in a ciliopathy cohort. \nSources: Literature",
"entity_name": "EXOC3L2",
"entity_type": "gene"
},
{
"created": "2019-12-20T16:59:31.923068+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Atypical Haemolytic Uraemic Syndrome_KidGen_VCGS to Atypical Haemolytic Uraemic Syndrome_KidGen_VCGS_RMH",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-20T16:41:29.331307+11:00",
"panel_name": "Kidneyome_SuperPanel_KidGen_VCGS",
"panel_id": 275,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added Panel Kidneyome_SuperPanel_KidGen_VCGS\nSet child panels to: Proteinuria_VCGS_KidGen; Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS; Renal amyloidosis_KidGen_VCGS; Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic_VCGS; Renal abnormalities of magnesium metabolism_KidGen_VCGS; Renal macrocystic disease_KidGen_VCGS; Atypical Haemolytic Uraemic Syndrome_VCGS; Metabolic renal disease_KidGen; Renal ciliopathies and nephronophthisis_KidGen; Haematuria_VCGS_KidGen; Renal tubulointerstitial disease_KidGen_VCGS; Renal abnormalities of calcium and phosphate metabolism_KidGen_VCGS; Renal tubulopathies_KidGen; Nephrolithiasis and Nephrocalcinosis_VCGS; Renal hypertension and disorders of aldosterone metabolism_KidGen_VCGS; Bartter Syndrome_VCGS; Renal tubular dysgenesis_VCGS; Branchio-oto-renal syndrome_VCGS; Alport syndrome_VCGS; Dent disease_VCGS; Hyperoxaluria_VCGS\nSet panel types to: Superpanel",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-20T16:20:34.259260+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMACHC as ready",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2019-12-20T16:20:34.252198+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmachc has been classified as Green List (High Evidence).",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2019-12-20T16:20:26.217476+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MMACHC as Green List (high evidence)",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2019-12-20T16:20:26.209178+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmachc has been classified as Green List (High Evidence).",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2019-12-20T16:19:57.157036+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_VCGS",
"panel_id": 211,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MMACHC was added\ngene: MMACHC was added to Atypical Haemolytic Uraemic Syndrome_VCGS. Sources: Expert list\nMode of inheritance for gene: MMACHC was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: MMACHC were set to Methylmalonic aciduria and homocystinuria, cblC type, MIM#277400\nReview for gene: MMACHC was set to GREEN\nAdded comment: HUS is a described feature of this metabolic condition. \nSources: Expert list",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2019-12-20T15:54:03.778320+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CFHR5: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Nephropathy due to CFHR5 deficiency, MIM#614809; Mode of inheritance: None",
"entity_name": "CFHR5",
"entity_type": "gene"
},
{
"created": "2019-12-20T15:52:08.332369+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CFH as ready",
"entity_name": "CFH",
"entity_type": "gene"
}
]
}