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{
"count": 220212,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2200",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2198",
"results": [
{
"created": "2019-11-17T16:28:33.429621+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PRRT2 was added\ngene: PRRT2 was added to Alternating hemiplegia including hemiplegic migraine_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PRRT2 was set to Unknown",
"entity_name": "PRRT2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:33.363061+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PNKD was added\ngene: PNKD was added to Alternating hemiplegia including hemiplegic migraine_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PNKD was set to Unknown",
"entity_name": "PNKD",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:33.296120+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNK18 was added\ngene: KCNK18 was added to Alternating hemiplegia including hemiplegic migraine_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNK18 was set to Unknown",
"entity_name": "KCNK18",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:33.229892+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KCNA1 was added\ngene: KCNA1 was added to Alternating hemiplegia including hemiplegic migraine_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KCNA1 was set to Unknown",
"entity_name": "KCNA1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:33.163799+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CACNB4 was added\ngene: CACNB4 was added to Alternating hemiplegia including hemiplegic migraine_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CACNB4 was set to Unknown",
"entity_name": "CACNB4",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:33.097245+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CACNA1A was added\ngene: CACNA1A was added to Alternating hemiplegia including hemiplegic migraine_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CACNA1A was set to Unknown",
"entity_name": "CACNA1A",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:32.969281+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ATP1A3 was added\ngene: ATP1A3 was added to Alternating hemiplegia including hemiplegic migraine_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ATP1A3 was set to Unknown",
"entity_name": "ATP1A3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:32.902269+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ATP1A2 was added\ngene: ATP1A2 was added to Alternating hemiplegia including hemiplegic migraine_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ATP1A2 was set to Unknown",
"entity_name": "ATP1A2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:32.860824+11:00",
"panel_name": "Alternating hemiplegia including hemiplegic migraine_VCGS",
"panel_id": 40,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Alternating hemiplegia including hemiplegic migraine_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:28:17.062168+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: OCRL was added\ngene: OCRL was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: OCRL was set to Unknown",
"entity_name": "OCRL",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.990834+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NPHS2 was added\ngene: NPHS2 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NPHS2 was set to Unknown",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.922884+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MYH9 was added\ngene: MYH9 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: MYH9 was set to Unknown",
"entity_name": "MYH9",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.855710+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LMX1B was added\ngene: LMX1B was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LMX1B was set to Unknown",
"entity_name": "LMX1B",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.789486+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FN1 was added\ngene: FN1 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: FN1 was set to Unknown",
"entity_name": "FN1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.722396+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CUBN was added\ngene: CUBN was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CUBN was set to Unknown",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.654557+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COL4A5 was added\ngene: COL4A5 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL4A5 was set to Unknown",
"entity_name": "COL4A5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.586729+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COL4A4 was added\ngene: COL4A4 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL4A4 was set to Unknown",
"entity_name": "COL4A4",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.518877+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COL4A3 was added\ngene: COL4A3 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL4A3 was set to Unknown",
"entity_name": "COL4A3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.452150+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COL4A2 was added\ngene: COL4A2 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL4A2 was set to Unknown",
"entity_name": "COL4A2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.384316+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COL4A1 was added\ngene: COL4A1 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: COL4A1 was set to Unknown",
"entity_name": "COL4A1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.317573+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CLCN5 was added\ngene: CLCN5 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CLCN5 was set to Unknown",
"entity_name": "CLCN5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.251256+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CFHR5 was added\ngene: CFHR5 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CFHR5 was set to Unknown",
"entity_name": "CFHR5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.184615+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CFH was added\ngene: CFH was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CFH was set to Unknown",
"entity_name": "CFH",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.115317+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CD151 was added\ngene: CD151 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CD151 was set to Unknown",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:28:16.073746+11:00",
"panel_name": "Alport syndrome extended_VCGS",
"panel_id": 39,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Alport syndrome extended_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:27:20.490593+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TYRP1 was added\ngene: TYRP1 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TYRP1 was set to Unknown",
"entity_name": "TYRP1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:20.420880+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TYR was added\ngene: TYR was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TYR was set to Unknown",
"entity_name": "TYR",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:20.351017+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC45A2 was added\ngene: SLC45A2 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC45A2 was set to Unknown",
"entity_name": "SLC45A2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:20.281665+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC24A5 was added\ngene: SLC24A5 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC24A5 was set to Unknown",
"entity_name": "SLC24A5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:20.213073+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: OCA2 was added\ngene: OCA2 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: OCA2 was set to Unknown",
"entity_name": "OCA2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:20.145436+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MC1R was added\ngene: MC1R was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: MC1R was set to Unknown",
"entity_name": "MC1R",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:20.005441+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LYST was added\ngene: LYST was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LYST was set to Unknown",
"entity_name": "LYST",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.937821+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LRMDA was added\ngene: LRMDA was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LRMDA was set to Unknown",
"entity_name": "LRMDA",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.869052+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS6 was added\ngene: HPS6 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HPS6 was set to Unknown",
"entity_name": "HPS6",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.801170+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS5 was added\ngene: HPS5 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HPS5 was set to Unknown",
"entity_name": "HPS5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.730150+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS4 was added\ngene: HPS4 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HPS4 was set to Unknown",
"entity_name": "HPS4",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.661333+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS3 was added\ngene: HPS3 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HPS3 was set to Unknown",
"entity_name": "HPS3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.592308+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HPS1 was added\ngene: HPS1 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HPS1 was set to Unknown",
"entity_name": "HPS1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.524719+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GPR143 was added\ngene: GPR143 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GPR143 was set to Unknown",
"entity_name": "GPR143",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.442669+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DTNBP1 was added\ngene: DTNBP1 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: DTNBP1 was set to Unknown",
"entity_name": "DTNBP1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.374979+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BLOC1S6 was added\ngene: BLOC1S6 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BLOC1S6 was set to Unknown",
"entity_name": "BLOC1S6",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.305520+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BLOC1S3 was added\ngene: BLOC1S3 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: BLOC1S3 was set to Unknown",
"entity_name": "BLOC1S3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.237804+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AP3B1 was added\ngene: AP3B1 was added to Ocular and oculocutaneous albinism_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AP3B1 was set to Unknown",
"entity_name": "AP3B1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:19.195844+11:00",
"panel_name": "Ocular and oculocutaneous albinism_VCGS",
"panel_id": 37,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Ocular and oculocutaneous albinism_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:27:06.275628+11:00",
"panel_name": "Alagille syndrome_VCGS",
"panel_id": 36,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NOTCH2 was added\ngene: NOTCH2 was added to Alagille syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NOTCH2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NOTCH2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:06.204392+11:00",
"panel_name": "Alagille syndrome_VCGS",
"panel_id": 36,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: JAG1 was added\ngene: JAG1 was added to Alagille syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: JAG1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "JAG1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:27:06.155508+11:00",
"panel_name": "Alagille syndrome_VCGS",
"panel_id": 36,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Alagille syndrome_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:17:59.066552+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WNT1 was added\ngene: WNT1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WNT1 was set to Unknown",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.983149+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WDR60 was added\ngene: WDR60 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WDR60 was set to Unknown",
"entity_name": "WDR60",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.898610+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WDR35 was added\ngene: WDR35 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WDR35 was set to Unknown",
"entity_name": "WDR35",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.813241+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WDR34 was added\ngene: WDR34 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WDR34 was set to Unknown",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.730667+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WDR19 was added\ngene: WDR19 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: WDR19 was set to Unknown",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.646194+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TTC21B was added\ngene: TTC21B was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TTC21B was set to Unknown",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.563857+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRPV6 was added\ngene: TRPV6 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TRPV6 was set to Unknown",
"entity_name": "TRPV6",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.480653+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRPV4 was added\ngene: TRPV4 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TRPV4 was set to Unknown",
"entity_name": "TRPV4",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.397814+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRIP11 was added\ngene: TRIP11 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TRIP11 was set to Unknown",
"entity_name": "TRIP11",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.315832+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM38B was added\ngene: TMEM38B was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TMEM38B was set to Unknown",
"entity_name": "TMEM38B",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.231936+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TCTN3 was added\ngene: TCTN3 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TCTN3 was set to Unknown",
"entity_name": "TCTN3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.145968+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TCTEX1D2 was added\ngene: TCTEX1D2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TCTEX1D2 was set to Unknown",
"entity_name": "TCTEX1D2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:58.060713+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TBX6 was added\ngene: TBX6 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: TBX6 was set to Unknown",
"entity_name": "TBX6",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.977153+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SP7 was added\ngene: SP7 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SP7 was set to Unknown",
"entity_name": "SP7",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.895197+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SOX9 was added\ngene: SOX9 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SOX9 was set to Unknown",
"entity_name": "SOX9",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.812275+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC35D1 was added\ngene: SLC35D1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC35D1 was set to Unknown",
"entity_name": "SLC35D1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.730243+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC26A2 was added\ngene: SLC26A2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SLC26A2 was set to Unknown",
"entity_name": "SLC26A2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.648890+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SERPINH1 was added\ngene: SERPINH1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SERPINH1 was set to Unknown",
"entity_name": "SERPINH1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.564973+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SERPINF1 was added\ngene: SERPINF1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SERPINF1 was set to Unknown",
"entity_name": "SERPINF1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.484294+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SBDS was added\ngene: SBDS was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SBDS was set to Unknown",
"entity_name": "SBDS",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.403767+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RNU4ATAC was added\ngene: RNU4ATAC was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: RNU4ATAC was set to Unknown",
"entity_name": "RNU4ATAC",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.323225+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RMRP was added\ngene: RMRP was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: RMRP was set to Unknown",
"entity_name": "RMRP",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.242392+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PTH1R was added\ngene: PTH1R was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PTH1R was set to Unknown",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.159994+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PPIB was added\ngene: PPIB was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PPIB was set to Unknown",
"entity_name": "PPIB",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:57.023635+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLS3 was added\ngene: PLS3 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PLS3 was set to Unknown",
"entity_name": "PLS3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.942105+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PLOD2 was added\ngene: PLOD2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PLOD2 was set to Unknown",
"entity_name": "PLOD2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.858695+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PEX7 was added\ngene: PEX7 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: PEX7 was set to Unknown",
"entity_name": "PEX7",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.777525+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: P3H1 was added\ngene: P3H1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: P3H1 was set to Unknown",
"entity_name": "P3H1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.697153+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: OFD1 was added\ngene: OFD1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: OFD1 was set to Unknown",
"entity_name": "OFD1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.616904+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NSDHL was added\ngene: NSDHL was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NSDHL was set to Unknown",
"entity_name": "NSDHL",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.537611+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NKX3-2 was added\ngene: NKX3-2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NKX3-2 was set to Unknown",
"entity_name": "NKX3-2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.458419+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NEK1 was added\ngene: NEK1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NEK1 was set to Unknown",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.378556+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MMP9 was added\ngene: MMP9 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: MMP9 was set to Unknown",
"entity_name": "MMP9",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.298327+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MMP13 was added\ngene: MMP13 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: MMP13 was set to Unknown",
"entity_name": "MMP13",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.218943+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MESP2 was added\ngene: MESP2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: MESP2 was set to Unknown",
"entity_name": "MESP2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.138119+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LRP5 was added\ngene: LRP5 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LRP5 was set to Unknown",
"entity_name": "LRP5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:56.055843+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LIFR was added\ngene: LIFR was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LIFR was set to Unknown",
"entity_name": "LIFR",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.975740+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LFNG was added\ngene: LFNG was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LFNG was set to Unknown",
"entity_name": "LFNG",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.897533+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LBR was added\ngene: LBR was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LBR was set to Unknown",
"entity_name": "LBR",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.818764+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KIF7 was added\ngene: KIF7 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KIF7 was set to Unknown",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.740424+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KIAA0586 was added\ngene: KIAA0586 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: KIAA0586 was set to Unknown",
"entity_name": "KIAA0586",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.661415+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: INPPL1 was added\ngene: INPPL1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: INPPL1 was set to Unknown",
"entity_name": "INPPL1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.580645+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT81 was added\ngene: IFT81 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: IFT81 was set to Unknown",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.499979+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT80 was added\ngene: IFT80 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: IFT80 was set to Unknown",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.422684+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT52 was added\ngene: IFT52 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: IFT52 was set to Unknown",
"entity_name": "IFT52",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.345688+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT43 was added\ngene: IFT43 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: IFT43 was set to Unknown",
"entity_name": "IFT43",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.266051+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT172 was added\ngene: IFT172 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: IFT172 was set to Unknown",
"entity_name": "IFT172",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.185616+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT140 was added\ngene: IFT140 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: IFT140 was set to Unknown",
"entity_name": "IFT140",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:55.106296+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT122 was added\ngene: IFT122 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: IFT122 was set to Unknown",
"entity_name": "IFT122",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:54.996538+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFITM5 was added\ngene: IFITM5 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: IFITM5 was set to Unknown",
"entity_name": "IFITM5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:54.918797+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ICK was added\ngene: ICK was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: ICK was set to Unknown",
"entity_name": "ICK",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:54.841099+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HYLS1 was added\ngene: HYLS1 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HYLS1 was set to Unknown",
"entity_name": "HYLS1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:17:54.764767+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: HSPG2 was added\ngene: HSPG2 was added to Skeletal dysplasia Fetal_MelbourneGenomics_VCGS. Sources: Melbourne Genomics Health Alliance Perinatal Autopsy Flagship,Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HSPG2 was set to Unknown",
"entity_name": "HSPG2",
"entity_type": "gene"
}
]
}