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{
"created": "2021-01-05T21:22:52.346667+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5965",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STX3 were changed from to Microvillus inclusion disease",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:22:26.518657+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STX3 as ready",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:22:26.498071+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stx3 has been classified as Green List (High Evidence).",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:22:18.589439+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STX3 were set to ",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:22:09.620156+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STX3 were changed from to Microvillus inclusion disease",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:21:59.229632+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STX3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:21:27.140183+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 24726755, 29266534, 25358429, 29282386, 30909251, 29282386; Phenotypes: Microvillus inclusion disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:21:26.590806+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STX3 were set to ",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:20:53.103790+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STX3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:20:18.174044+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 24726755, 29266534, 25358429, 29282386, 30909251, 29282386; Phenotypes: Microvillus inclusion disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STX3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:17:12.591630+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPINT2 as ready",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:17:12.581422+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spint2 has been classified as Green List (High Evidence).",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:17:05.244735+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SPINT2 were changed from to Diarrhoea 3, secretory sodium, congenital, syndromic 270420",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:16:45.838835+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPINT2 were set to ",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:16:27.316346+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SPINT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:16:06.783077+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SPINT2: Rating: GREEN; Mode of pathogenicity: None; Publications: 24142340, 30445423; Phenotypes: Diarrhoea 3, secretory sodium, congenital, syndromic 270420; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:15:44.229155+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPINT2 as ready",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:15:44.220188+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spint2 has been classified as Green List (High Evidence).",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:15:17.046486+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SPINT2 were changed from to Diarrhoea 3, secretory sodium, congenital, syndromic 270420",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:14:40.705523+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPINT2 were set to ",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:14:13.868341+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SPINT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:13:45.804212+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SPINT2: Rating: GREEN; Mode of pathogenicity: None; Publications: 24142340, 30445423; Phenotypes: Diarrhoea 3, secretory sodium, congenital, syndromic 270420; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:12:20.424053+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC9A3 as ready",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:12:20.413297+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc9a3 has been classified as Green List (High Evidence).",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:12:10.679029+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC9A3 as ready",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:12:10.670702+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc9a3 has been classified as Green List (High Evidence).",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:12:03.884029+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC9A3 were changed from to Diarrhoea 8, secretory sodium, congenital 616868",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:11:44.909491+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC9A3 were set to ",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:11:26.242084+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5957",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC9A3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:11:15.122472+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC9A3 were changed from to Diarrhoea 8, secretory sodium, congenital 616868",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:11:03.095749+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC9A3: Rating: GREEN; Mode of pathogenicity: None; Publications: 30633106, 31276831, 26358773; Phenotypes: Diarrhoea 8, secretory sodium, congenital 616868; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:10:24.743665+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC9A3 were set to ",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:09:56.068794+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC9A3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:09:25.311379+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC9A3: Rating: GREEN; Mode of pathogenicity: None; Publications: 30633106, 31276831, 26358773; Phenotypes: Diarrhoea 8, secretory sodium, congenital 616868; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC9A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:07:29.792284+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC7A7 as ready",
"entity_name": "SLC7A7",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:07:29.773259+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc7a7 has been classified as Green List (High Evidence).",
"entity_name": "SLC7A7",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:07:27.305323+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC7A7 were changed from to Lysinuric protein intolerance, MIM# 222700",
"entity_name": "SLC7A7",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:06:56.414690+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC7A7 were set to ",
"entity_name": "SLC7A7",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:06:28.524274+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC7A7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC7A7",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:05:57.545880+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC7A7: Rating: GREEN; Mode of pathogenicity: None; Publications: 10080182, 18716612; Phenotypes: Lysinuric protein intolerance, MIM# 222700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC7A7",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:03:48.726678+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC5A1 as ready",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:03:48.714276+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc5a1 has been classified as Green List (High Evidence).",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:02:45.986788+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC5A1 were changed from to Glucose/galactose malabsorption, MIM# 606824",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:02:13.642634+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC5A1 as ready",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:02:13.634698+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc5a1 has been classified as Green List (High Evidence).",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:02:05.908339+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC5A1 were changed from to Glucose/galactose malabsorption, MIM# 606824",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:01:47.146235+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5955",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC5A1 were set to ",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:01:25.204461+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5954",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC5A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:01:05.493503+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5953",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC5A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20486940, 32946683; Phenotypes: Glucose/galactose malabsorption, MIM# 606824; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:01:04.023248+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC5A1 were set to ",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T21:00:31.766813+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC5A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:59:56.590524+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC5A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20486940, 32946683; Phenotypes: Glucose/galactose malabsorption, MIM# 606824; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC5A1",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:57:35.316344+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC39A4 as ready",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:57:35.305230+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a4 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:57:32.126560+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC39A4 were changed from to Acrodermatitis enteropathica, MIM# 201100",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:57:03.078923+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5953",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC39A4 as ready",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:57:03.069726+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5953",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a4 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:56:56.065210+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5953",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC39A4 were changed from to Acrodermatitis enteropathica, MIM# 201100",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:56:38.618327+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5952",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC39A4 were set to ",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:56:21.242018+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5951",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC39A4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:56:03.240164+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC39A4 were set to ",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:55:59.534899+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC39A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 19370757; Phenotypes: Acrodermatitis enteropathica, MIM# 201100; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:55:23.641736+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC39A4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:54:54.613337+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC39A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 19370757; Phenotypes: Acrodermatitis enteropathica, MIM# 201100; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:53:31.896673+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC2A2 as ready",
"entity_name": "SLC2A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:53:31.887838+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc2a2 has been classified as Red List (Low Evidence).",
"entity_name": "SLC2A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:53:28.132437+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC2A2 were changed from to Fanconi-Bickel syndrome, MIM# 227810",
"entity_name": "SLC2A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:52:54.769012+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC2A2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC2A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:52:28.146121+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC2A2 as Red List (low evidence)",
"entity_name": "SLC2A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:52:28.138344+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc2a2 has been classified as Red List (Low Evidence).",
"entity_name": "SLC2A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:52:00.439782+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC2A2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi-Bickel syndrome, MIM# 227810; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC2A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:48:30.587052+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC26A3 as ready",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:48:30.579514+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc26a3 has been classified as Green List (High Evidence).",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:48:22.937955+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC26A3 were changed from to Diarrhoea 1, secretory chloride, congenital, MIM# 214700",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:48:04.779232+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC26A3 as ready",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:48:04.769447+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc26a3 has been classified as Green List (High Evidence).",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:48:01.488145+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC26A3 were changed from to Diarrhoea 1, secretory chloride, congenital, MIM# 214700",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:47:29.541201+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC26A3 were set to ",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:47:11.062912+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5948",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC26A3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:46:54.828197+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC26A3 were set to ",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:46:52.415012+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC26A3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31325522, 19861545, 11524734; Phenotypes: Diarrhoea 1, secretory chloride, congenital, MIM# 214700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:46:34.900937+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC26A3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:46:14.521031+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC26A3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:45:40.651888+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC26A3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31325522, 19861545, 11524734; Phenotypes: Diarrhoea 1, secretory chloride, congenital, MIM# 214700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:43:16.415678+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC51B as ready",
"entity_name": "SLC51B",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:43:16.407811+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc51b has been classified as Red List (Low Evidence).",
"entity_name": "SLC51B",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:43:05.842744+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC51B was added\ngene: SLC51B was added to Mendeliome. Sources: Expert Review\nMode of inheritance for gene: SLC51B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC51B were set to 28898457\nPhenotypes for gene: SLC51B were set to Congenital diarrhoea; Cholestasis\nReview for gene: SLC51B was set to RED\nAdded comment: Two siblings reported with homozygous LOF variant in this gene and congenital diarrhoea/cholestasis. \nSources: Expert Review",
"entity_name": "SLC51B",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:42:50.779010+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC51B as ready",
"entity_name": "SLC51B",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:42:50.768959+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc51b has been classified as Red List (Low Evidence).",
"entity_name": "SLC51B",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:42:02.140218+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC51B was added\ngene: SLC51B was added to Congenital Diarrhoea. Sources: Expert Review\nMode of inheritance for gene: SLC51B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC51B were set to 28898457\nPhenotypes for gene: SLC51B were set to Congenital diarrhoea; Cholestasis\nReview for gene: SLC51B was set to RED\nAdded comment: Two siblings reported with homozygous LOF variant in this gene and congenital diarrhoea/cholestasis. \nSources: Expert Review",
"entity_name": "SLC51B",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:39:13.755949+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC10A2 as ready",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:39:13.745662+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5946",
"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": "2021-01-05T20:39:06.646374+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5946",
"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": "2021-01-05T20:38:48.335660+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5945",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC10A2 were set to ",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:38:33.297860+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5944",
"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": "2021-01-05T20:38:14.161572+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC10A2 as Red List (low evidence)",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:38:14.153782+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5943",
"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": "2021-01-05T20:37:55.569425+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5942",
"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": "2021-01-05T20:37:12.543828+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC10A2 as ready",
"entity_name": "SLC10A2",
"entity_type": "gene"
},
{
"created": "2021-01-05T20:37:12.532772+11:00",
"panel_name": "Congenital Diarrhoea",
"panel_id": 89,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc10a2 has been classified as Red List (Low Evidence).",
"entity_name": "SLC10A2",
"entity_type": "gene"
}
]
}