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{
"count": 220314,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1451",
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"results": [
{
"created": "2021-01-05T20:37:09.515806+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC10A2 were changed from to Bile acid malabsorption, primary, MIM# 613291",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:36:45.908195+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC10A2 were set to ",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:36:23.047503+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC10A2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:35:54.435027+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC10A2 as Red List (low evidence)",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:35:54.425142+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc10a2 has been classified as Red List (Low Evidence).",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:35:26.412862+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC10A2: Rating: RED; Mode of pathogenicity: None; Publications: 9109432; Phenotypes: Bile acid malabsorption, primary, MIM# 613291; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:30:31.394009+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SKIV2L as ready",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:30:31.383581+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: skiv2l has been classified as Green List (High Evidence).",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:28:23.006085+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SKIV2L were changed from to Trichohepatoenteric syndrome 2, MIM# 614602",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:27:55.753778+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SKIV2L were set to ",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:27:24.981754+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SKIV2L was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:26:57.753604+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SKIV2L: Rating: GREEN; Mode of pathogenicity: None; Publications: 22444670, 33114497, 30397475, 29527791, 29484573; Phenotypes: Trichohepatoenteric syndrome 2, MIM# 614602; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:23:58.475359+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5942",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLVAP as ready",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:23:58.464010+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5942",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plvap has been classified as Green List (High Evidence).",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:23:50.359263+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SI as ready",
"entity_name": "SI",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:23:50.348769+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: si has been classified as Green List (High Evidence).",
"entity_name": "SI",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:23:47.301527+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SI were set to ",
"entity_name": "SI",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:23:17.202850+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SI were changed from to Sucrase-isomaltase deficiency, congenital, MIM# 222900",
"entity_name": "SI",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:22:49.816444+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SI was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SI",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:22:19.329994+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SI: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Sucrase-isomaltase deficiency, congenital, MIM# 222900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SI",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:21:27.927752+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SBDS as ready",
"entity_name": "SBDS",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:21:27.913465+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sbds has been classified as Green List (High Evidence).",
"entity_name": "SBDS",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:18:34.603133+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SBDS were changed from to Shwachman-Diamond syndrome, MIM# 260400",
"entity_name": "SBDS",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:16:25.200617+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SBDS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SBDS",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:15:56.792723+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SBDS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Shwachman-Diamond syndrome, MIM# 260400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SBDS",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:45:00.357347+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SAR1B as ready",
"entity_name": "SAR1B",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:45:00.347156+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sar1b has been classified as Green List (High Evidence).",
"entity_name": "SAR1B",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:44:55.278550+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SAR1B were changed from to Chylomicron retention disease, MIM# 246700",
"entity_name": "SAR1B",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:44:24.486406+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SAR1B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SAR1B",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:43:55.338562+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SAR1B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Chylomicron retention disease, MIM# 246700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SAR1B",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:42:08.009528+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRSS1 as ready",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:42:07.998574+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prss1 has been classified as Green List (High Evidence).",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:41:58.412422+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRSS1 were changed from to Pancreatitis, hereditary, MIM# 167800",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:41:30.455872+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRSS1 were set to ",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:40:38.682048+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRSS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:40:08.035737+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRSS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22379635; Phenotypes: Pancreatitis, hereditary, MIM# 167800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:35:32.943249+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5942",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PLVAP were changed from to Diarrhoea 10, protein-losing enteropathy type, MIM# 618183",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:35:14.722381+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5941",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PLVAP were set to ",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:34:54.305715+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PLVAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:34:34.685294+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5939",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PLVAP: Rating: GREEN; Mode of pathogenicity: None; Publications: 29875123, 29661969, 26207260, 31215290; Phenotypes: Diarrhoea 10, protein-losing enteropathy type, MIM# 618183; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:34:23.288887+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLVAP as ready",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:34:23.280238+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plvap has been classified as Green List (High Evidence).",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:33:53.538850+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PLVAP were changed from to Diarrhoea 10, protein-losing enteropathy type, MIM# 618183",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:33:22.457942+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PLVAP were set to ",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:32:54.521313+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PLVAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T19:32:25.914792+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PLVAP: Rating: GREEN; Mode of pathogenicity: None; Publications: 29875123, 29661969, 26207260, 31215290; Phenotypes: Diarrhea 10, protein-losing enteropathy type, MIM# 618183; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PLVAP",
"entity_type": "gene"
},
{
"created": "2021-01-05T16:30:48.173072+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PCSK1 as ready",
"entity_name": "PCSK1",
"entity_type": "gene"
},
{
"created": "2021-01-05T16:30:48.162705+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pcsk1 has been classified as Green List (High Evidence).",
"entity_name": "PCSK1",
"entity_type": "gene"
},
{
"created": "2021-01-05T13:16:13.325001+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PCSK1 were changed from to Obesity with impaired prohormone processing, MIM# 600955",
"entity_name": "PCSK1",
"entity_type": "gene"
},
{
"created": "2021-01-05T13:15:45.050565+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PCSK1 were set to ",
"entity_name": "PCSK1",
"entity_type": "gene"
},
{
"created": "2021-01-05T13:15:14.342579+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PCSK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PCSK1",
"entity_type": "gene"
},
{
"created": "2021-01-05T13:14:46.315981+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PCSK1: Rating: GREEN; Mode of pathogenicity: None; Publications: 14617756, 17595246; Phenotypes: Obesity with impaired prohormone processing, MIM# 600955; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PCSK1",
"entity_type": "gene"
},
{
"created": "2021-01-05T13:06:42.840131+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEUROG3 as ready",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T13:06:42.831789+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neurog3 has been classified as Green List (High Evidence).",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T13:05:45.492592+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEUROG3 were changed from Diarrhea 4, malabsorptive, congenital to Diarrhoea 4, malabsorptive, congenital, MIM# 610370",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T13:05:34.183307+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEUROG3 were set to ",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:59:28.418771+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NEUROG3 as Green List (high evidence)",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:59:28.406827+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neurog3 has been classified as Green List (High Evidence).",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:59:15.852182+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEUROG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 16855267, 32574610, 28724572, 21490072; Phenotypes: Diarrhoea 4, malabsorptive, congenital, MIM# 610370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:56:26.707180+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5939",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEUROG3 as ready",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:56:26.684034+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5939",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neurog3 has been classified as Green List (High Evidence).",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:56:17.729143+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5939",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEUROG3 were changed from to Diarrhoea 4, malabsorptive, congenital, MIM# 610370",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:55:51.191914+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5938",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEUROG3 were set to ",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:55:15.921750+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5937",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NEUROG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:53:56.383652+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEUROG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 16855267, 32574610, 28724572, 21490072; Phenotypes: Diarrhoea 4, malabsorptive, congenital, MIM# 610370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:51:42.171407+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEUROG3 as ready",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:51:42.162377+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neurog3 has been classified as Green List (High Evidence).",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:51:23.933622+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEUROG3 were changed from to Diarrhoea 4, malabsorptive, congenital, MIM# 610370",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:51:00.337149+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEUROG3 were set to ",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:49:12.784830+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NEUROG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:48:43.602493+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NEUROG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 16855267, 32574610, 28724572, 21490072; Phenotypes: Diarrhea 4, malabsorptive, congenital, MIM# 610370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NEUROG3",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:44:39.347822+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GUCY2C as ready",
"entity_name": "GUCY2C",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:44:39.339276+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gucy2c has been classified as Green List (High Evidence).",
"entity_name": "GUCY2C",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:44:35.719514+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GUCY2C were changed from to Diarrhoea 6, MIM# 614616",
"entity_name": "GUCY2C",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:43:45.706431+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GUCY2C were set to ",
"entity_name": "GUCY2C",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:43:17.320981+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: GUCY2C was changed from to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
"entity_name": "GUCY2C",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:41:42.625074+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GUCY2C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GUCY2C",
"entity_type": "gene"
},
{
"created": "2021-01-05T12:41:13.118005+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GUCY2C: Rating: GREEN; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 22521417, 22436048, 25994218, 30353760, 28957388; Phenotypes: Diarrhoea 6, MIM# 614616; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GUCY2C",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:15:22.407782+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMPRSS15 as ready",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:15:22.398925+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmprss15 has been classified as Green List (High Evidence).",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:15:19.598973+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMPRSS15 were changed from to Enterokinase deficiency, MIM# 226200",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:14:55.593167+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMPRSS15 as ready",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:14:55.581997+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmprss15 has been classified as Green List (High Evidence).",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:14:48.285525+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMPRSS15 were changed from to Enterokinase deficiency, MIM# 226200",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:14:29.822627+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5935",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMPRSS15 were set to ",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:14:11.721776+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5934",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TMPRSS15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:13:55.539718+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMPRSS15 were set to ",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:13:52.605244+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TMPRSS15: Rating: GREEN; Mode of pathogenicity: None; Publications: 11719902, 33061943; Phenotypes: Enterokinase deficiency, MIM# 226200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:13:18.687271+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TMPRSS15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:10:54.023019+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TMPRSS15: Rating: GREEN; Mode of pathogenicity: None; Publications: 11719902, 33061943; Phenotypes: Enterokinase deficiency, MIM# 226200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMPRSS15",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:06:20.922160+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC37 as ready",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:06:20.913735+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc37 has been classified as Green List (High Evidence).",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:06:09.315883+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC37 were changed from to Trichohepatoenteric syndrome 1, MIM# 222470",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:05:51.237757+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5932",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC37 were set to ",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:05:33.198951+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5931",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TTC37 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:05:13.106608+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5930",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TTC37: Rating: GREEN; Mode of pathogenicity: None; Publications: 20176027, 17318842; Phenotypes: Trichohepatoenteric syndrome 1, MIM# 222470; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:04:54.893155+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC37 as ready",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:04:54.879346+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc37 has been classified as Green List (High Evidence).",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:04:43.447703+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC37 were changed from to Trichohepatoenteric syndrome 1, MIM# 222470",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2021-01-05T11:04:15.109022+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC37 were set to ",
"entity_name": "TTC37",
"entity_type": "gene"
}
]
}