{"count":220212,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2200","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&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"}]}