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{
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"text": "removed gene:TRPM1 from the panel",
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{
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"text": "removed gene:THAP1 from the panel",
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},
{
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"item_type": "panel",
"text": "removed gene:TH from the panel",
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{
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"text": "removed gene:TGM1 from the panel",
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},
{
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"item_type": "panel",
"text": "removed gene:TAT from the panel",
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},
{
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"panel_name": "Fetal anomalies",
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"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:TACR3 from the panel",
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{
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"item_type": "panel",
"text": "removed gene:SULT2B1 from the panel",
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{
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"panel_name": "Fetal anomalies",
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"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:STS from the panel",
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},
{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2158",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:STAT1 from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2157",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:ST14 from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2156",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:SPTLC2 from the panel",
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},
{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2155",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:SPRY4 from the panel",
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},
{
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"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2154",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:SPR from the panel",
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{
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"panel_name": "Fetal anomalies",
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"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:SLC6A5 from the panel",
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},
{
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"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2152",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:SLC6A3 from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2151",
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"item_type": "panel",
"text": "removed gene:SLC6A1 from the panel",
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{
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"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2150",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:SLC5A5 from the panel",
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},
{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2149",
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"item_type": "panel",
"text": "removed gene:SLC4A11 from the panel",
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},
{
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"panel_name": "Fetal anomalies",
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"text": "removed gene:SLC4A1 from the panel",
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{
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"item_type": "panel",
"text": "removed gene:SLC25A22 from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2146",
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"item_type": "panel",
"text": "removed gene:SLC25A15 from the panel",
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{
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"panel_name": "Fetal anomalies",
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"text": "removed gene:SDR9C7 from the panel",
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{
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"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:SCN11A from the panel",
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{
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"panel_version": "0.2143",
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"item_type": "panel",
"text": "removed gene:RTN4IP1 from the panel",
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},
{
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"panel_name": "Fetal anomalies",
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"item_type": "panel",
"text": "removed gene:RSPO4 from the panel",
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{
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"panel_version": "0.2141",
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"item_type": "panel",
"text": "removed gene:RPGRIP1 from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2140",
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"item_type": "panel",
"text": "removed gene:RPE65 from the panel",
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{
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"panel_version": "0.2139",
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"text": "removed gene:RETREG1 from the panel",
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{
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"item_type": "panel",
"text": "removed gene:PYGL from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2137",
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"item_type": "panel",
"text": "removed gene:QDPR from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2136",
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"item_type": "panel",
"text": "removed gene:PRX from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2135",
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"item_type": "panel",
"text": "removed gene:PROP1 from the panel",
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{
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"panel_name": "Fetal anomalies",
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"panel_version": "0.2134",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PROKR2 from the panel",
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},
{
"created": "2022-01-13T20:07:16.099614+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2133",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PROK2 from the panel",
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{
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"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2132",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PRDM12 from the panel",
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},
{
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"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2131",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:POC1B from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:06:22.453319+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2130",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PNPT1 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:06:03.713555+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2129",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PNPLA1 from the panel",
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},
{
"created": "2022-01-13T20:05:46.856257+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2128",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PMS2 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:05:29.471260+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2127",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PMP22 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:05:01.205414+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2126",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PLCE1 from the panel",
"entity_name": null,
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},
{
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"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2125",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PLA2G6 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:04:22.487816+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2124",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PGK1 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:04:00.355895+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2123",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PDE6G from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:03:40.829146+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2122",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PCDH19 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:03:24.803323+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2121",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PCCB from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:03:11.919719+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2120",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PCCA from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:02:55.696779+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2119",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PCBD1 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:02:33.436448+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2118",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PC from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:02:17.788872+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2117",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PAX9 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:02:00.862478+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2116",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:PAH from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:01:44.965451+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2115",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:OXCT1 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:01:17.403478+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2114",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:OTULIN from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:01:02.593865+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2113",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:OTOGL from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T20:00:47.163231+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2112",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:OTC from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T20:00:29.233423+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2111",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:NTRK1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T19:59:51.402810+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2110",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:NSMF from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T19:59:31.096870+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2109",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:NPHS2 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T19:59:13.468949+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2108",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:NKX2-1 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T19:58:58.623043+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2107",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:NMNAT1 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T19:58:42.983717+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2106",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:NIPAL4 from the panel",
"entity_name": null,
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},
{
"created": "2022-01-13T19:58:18.101127+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2105",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:NAGS from the panel",
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},
{
"created": "2022-01-13T19:57:44.862839+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2104",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MTRR from the panel",
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},
{
"created": "2022-01-13T19:57:30.746775+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2103",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MTR from the panel",
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},
{
"created": "2022-01-13T19:57:05.079663+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2102",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MRE11 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T19:56:35.050312+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2101",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MICU1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T19:56:08.610787+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2100",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MFSD8 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T19:55:31.659320+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2099",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MCEE from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T19:55:10.234466+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2098",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MCCC2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T19:54:30.806033+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2097",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MCCC1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:39:55.584835+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2096",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MYO5B from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:39:42.302553+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2095",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MYO7A from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:39:28.853078+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2094",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MYH9 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:39:07.926209+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2093",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MUT from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:38:50.082500+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2092",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MTHFR from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:38:36.622861+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2091",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MT-TP from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:38:19.637761+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2090",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MSH6 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:38:05.740313+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2089",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MSH2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:37:51.618659+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2088",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MMADHC from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:37:36.298290+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2087",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MMAB from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:37:20.874041+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2086",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MMAA from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:37:07.618133+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2085",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MLH1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:36:39.968065+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2084",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:MC2R from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:35:49.686462+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2083",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:LAMC2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:35:13.061600+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2082",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:KCNB1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:34:46.597180+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2081",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:KCNA2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:33:55.868084+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2080",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:IVD from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:32:53.336925+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2079",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:HSD3B7 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:31:49.108167+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2078",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:HMGCS2 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:31:22.947672+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2077",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:HMGCL from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:31:00.490996+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2076",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:HEXB from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:30:26.696868+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2075",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:HEXA from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:30:02.823462+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2074",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "removed gene:HCN1 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2022-01-13T18:21:38.228223+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE4D as ready",
"entity_name": "PDE4D",
"entity_type": "gene"
},
{
"created": "2022-01-13T18:21:38.219119+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde4d has been classified as Green List (High Evidence).",
"entity_name": "PDE4D",
"entity_type": "gene"
},
{
"created": "2022-01-13T18:21:34.839375+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE4D were changed from ACRODYSOSTOSIS to Acrodysostosis 2, with or without hormone resistance, MIM# 614613",
"entity_name": "PDE4D",
"entity_type": "gene"
},
{
"created": "2022-01-13T18:21:15.511739+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2072",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDE4D was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PDE4D",
"entity_type": "gene"
},
{
"created": "2022-01-13T18:21:03.232917+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2071",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PDE4D: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Acrodysostosis 2, with or without hormone resistance, MIM# 614613; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PDE4D",
"entity_type": "gene"
},
{
"created": "2022-01-13T18:19:04.425768+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDCD10 as ready",
"entity_name": "PDCD10",
"entity_type": "gene"
},
{
"created": "2022-01-13T18:19:04.404552+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdcd10 has been classified as Green List (High Evidence).",
"entity_name": "PDCD10",
"entity_type": "gene"
}
]
}