{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=827","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=825","results":[{"created":"2022-05-20T16:17:57.765964+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14774","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AVPR2 as ready","entity_name":"AVPR2","entity_type":"gene"},{"created":"2022-05-20T16:17:57.754050+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14774","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: avpr2 has been classified as Green List (High Evidence).","entity_name":"AVPR2","entity_type":"gene"},{"created":"2022-05-20T16:17:32.555495+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14774","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DPY19L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPY19L2","entity_type":"gene"},{"created":"2022-05-20T16:17:23.250848+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14773","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AVP as ready","entity_name":"AVP","entity_type":"gene"},{"created":"2022-05-20T16:17:23.233712+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14773","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: avp has been classified as Green List (High Evidence).","entity_name":"AVP","entity_type":"gene"},{"created":"2022-05-20T16:16:46.953628+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14773","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AVP were changed from  to Diabetes insipidus, neurohypophyseal MIM#125700","entity_name":"AVP","entity_type":"gene"},{"created":"2022-05-20T16:16:46.534193+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14772","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DRAM2 as ready","entity_name":"DRAM2","entity_type":"gene"},{"created":"2022-05-20T16:16:46.517099+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14772","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dram2 has been classified as Green List (High Evidence).","entity_name":"DRAM2","entity_type":"gene"},{"created":"2022-05-20T16:16:36.767085+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14772","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DRAM2 were changed from  to Cone-rod dystrophy 21 - MIM#616502","entity_name":"DRAM2","entity_type":"gene"},{"created":"2022-05-20T16:16:16.412887+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14771","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AVP were set to ","entity_name":"AVP","entity_type":"gene"},{"created":"2022-05-20T16:16:00.443016+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14770","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DRAM2 were set to ","entity_name":"DRAM2","entity_type":"gene"},{"created":"2022-05-20T16:15:36.402582+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14769","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DRAM2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DRAM2","entity_type":"gene"},{"created":"2022-05-20T16:15:23.932942+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14768","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AVP was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"AVP","entity_type":"gene"},{"created":"2022-05-20T16:14:16.849700+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14767","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DRD2 as ready","entity_name":"DRD2","entity_type":"gene"},{"created":"2022-05-20T16:14:16.836934+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14767","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: drd2 has been classified as Red List (Low Evidence).","entity_name":"DRD2","entity_type":"gene"},{"created":"2022-05-20T16:14:03.573616+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14767","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATP6V1E1 as ready","entity_name":"ATP6V1E1","entity_type":"gene"},{"created":"2022-05-20T16:14:03.548648+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14767","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp6v1e1 has been classified as Green List (High Evidence).","entity_name":"ATP6V1E1","entity_type":"gene"},{"created":"2022-05-20T16:13:55.354277+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14767","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATP6V1E1 were changed from  to Cutis laxa, autosomal recessive, type IIC MIM#617402","entity_name":"ATP6V1E1","entity_type":"gene"},{"created":"2022-05-20T16:12:51.449244+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14766","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATP6V1E1 were set to ","entity_name":"ATP6V1E1","entity_type":"gene"},{"created":"2022-05-20T16:12:35.216700+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14765","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DRD2 as Red List (low evidence)","entity_name":"DRD2","entity_type":"gene"},{"created":"2022-05-20T16:12:35.193146+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14765","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: drd2 has been classified as Red List (Low Evidence).","entity_name":"DRD2","entity_type":"gene"},{"created":"2022-05-20T16:11:59.685316+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14764","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DRD3 as ready","entity_name":"DRD3","entity_type":"gene"},{"created":"2022-05-20T16:11:59.672913+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14764","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: drd3 has been classified as Red List (Low Evidence).","entity_name":"DRD3","entity_type":"gene"},{"created":"2022-05-20T16:11:55.750667+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14764","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ATP6V1E1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ATP6V1E1","entity_type":"gene"},{"created":"2022-05-20T16:11:41.804721+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14763","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DRD3 were changed from  to {Essential tremor, hereditary, 1} - MIM#190300; {Schizophrenia, susceptibility to} - MIM#181500","entity_name":"DRD3","entity_type":"gene"},{"created":"2022-05-20T16:11:03.867530+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14762","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DRD3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DRD3","entity_type":"gene"},{"created":"2022-05-20T16:10:44.034991+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14761","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DRD3 as Red List (low evidence)","entity_name":"DRD3","entity_type":"gene"},{"created":"2022-05-20T16:10:44.021795+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14761","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: drd3 has been classified as Red List (Low Evidence).","entity_name":"DRD3","entity_type":"gene"},{"created":"2022-05-20T16:10:40.937524+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14760","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATP2A1 as ready","entity_name":"ATP2A1","entity_type":"gene"},{"created":"2022-05-20T16:10:40.922746+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14760","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp2a1 has been classified as Green List (High Evidence).","entity_name":"ATP2A1","entity_type":"gene"},{"created":"2022-05-20T16:10:14.061111+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14760","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATP2A1 were changed from  to Brody myopathy, OMIM # 601003","entity_name":"ATP2A1","entity_type":"gene"},{"created":"2022-05-20T16:09:50.706170+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14759","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATP2A1 were set to ","entity_name":"ATP2A1","entity_type":"gene"},{"created":"2022-05-20T16:09:43.441107+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14758","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DSC3 as ready","entity_name":"DSC3","entity_type":"gene"},{"created":"2022-05-20T16:09:43.427466+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14758","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dsc3 has been classified as Amber List (Moderate Evidence).","entity_name":"DSC3","entity_type":"gene"},{"created":"2022-05-20T16:09:34.037260+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14758","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DSC3 were changed from  to Hypotrichosis and recurrent skin vesicles MIM#613102","entity_name":"DSC3","entity_type":"gene"},{"created":"2022-05-20T16:09:24.821357+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14757","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ATP2A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ATP2A1","entity_type":"gene"},{"created":"2022-05-20T16:07:38.825357+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14756","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DSC3 were set to ","entity_name":"DSC3","entity_type":"gene"},{"created":"2022-05-20T16:07:26.669109+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14755","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADD1 as ready","entity_name":"ADD1","entity_type":"gene"},{"created":"2022-05-20T16:07:26.652023+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14755","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: add1 has been classified as Green List (High Evidence).","entity_name":"ADD1","entity_type":"gene"},{"created":"2022-05-20T16:07:20.271406+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14755","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DSC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DSC3","entity_type":"gene"},{"created":"2022-05-20T16:07:08.444347+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14755","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADD1 were changed from Intellectual disability, corpus callosum dysgenesis, and ventriculomegaly; no OMIM # to Neurodevelopmental disorder MONDO:0700092, ADD1-related","entity_name":"ADD1","entity_type":"gene"},{"created":"2022-05-20T16:04:57.338020+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14754","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DSC3 as Amber List (moderate evidence)","entity_name":"DSC3","entity_type":"gene"},{"created":"2022-05-20T16:04:57.324014+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14754","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dsc3 has been classified as Amber List (Moderate Evidence).","entity_name":"DSC3","entity_type":"gene"},{"created":"2022-05-20T16:04:11.019932+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14753","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DSCAM as ready","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:04:10.998408+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14753","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dscam has been classified as Green List (High Evidence).","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:04:00.871450+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14753","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DSCAM were changed from  to Autism MONDO:0005260","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:03:17.267967+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14752","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DSCAM were set to ","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:02:55.938028+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14751","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DSCAM as Green List (high evidence)","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:02:55.926762+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14751","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dscam has been classified as Green List (High Evidence).","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:02:05.076210+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14750","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DSCAM was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:01:44.468520+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14749","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DSCAM as Amber List (moderate evidence)","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:01:44.456746+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14749","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dscam has been classified as Amber List (Moderate Evidence).","entity_name":"DSCAM","entity_type":"gene"},{"created":"2022-05-20T16:00:47.784198+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14748","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DSE as ready","entity_name":"DSE","entity_type":"gene"},{"created":"2022-05-20T16:00:47.768785+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14748","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dse has been classified as Green List (High Evidence).","entity_name":"DSE","entity_type":"gene"},{"created":"2022-05-20T16:00:39.531408+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14748","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DSE were changed from  to Ehlers-Danlos syndrome, musculocontractural type 2 - MIM#615539","entity_name":"DSE","entity_type":"gene"},{"created":"2022-05-20T16:00:18.893998+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14747","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DSE were set to ","entity_name":"DSE","entity_type":"gene"},{"created":"2022-05-20T15:59:58.063197+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14746","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DSE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DSE","entity_type":"gene"},{"created":"2022-05-20T15:59:00.932866+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14745","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DSG4 as ready","entity_name":"DSG4","entity_type":"gene"},{"created":"2022-05-20T15:59:00.920246+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14745","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dsg4 has been classified as Green List (High Evidence).","entity_name":"DSG4","entity_type":"gene"},{"created":"2022-05-20T15:58:51.996136+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14745","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DSG4 were changed from  to Hypotrichosis 6 - MIM#607903","entity_name":"DSG4","entity_type":"gene"},{"created":"2022-05-20T15:58:32.389823+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14744","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DSG4 were set to ","entity_name":"DSG4","entity_type":"gene"},{"created":"2022-05-20T15:58:11.089597+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14743","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DSG4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DSG4","entity_type":"gene"},{"created":"2022-05-20T15:57:30.721941+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14742","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DSPP as ready","entity_name":"DSPP","entity_type":"gene"},{"created":"2022-05-20T15:57:30.707725+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14742","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dspp has been classified as Green List (High Evidence).","entity_name":"DSPP","entity_type":"gene"},{"created":"2022-05-20T15:57:21.811931+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14742","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DSPP were changed from  to Deafness, autosomal dominant 39, with dentinogenesis - MIM#605594; Dentin dysplasia, type II - MIM#125420; Dentinogenesis imperfecta, Shields type II - MIM#125490; Dentinogenesis imperfecta, Shields type III - MIM#125500","entity_name":"DSPP","entity_type":"gene"},{"created":"2022-05-20T15:57:01.724459+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14741","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DSPP was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DSPP","entity_type":"gene"},{"created":"2022-05-20T15:56:21.590036+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14740","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DUOX2 as ready","entity_name":"DUOX2","entity_type":"gene"},{"created":"2022-05-20T15:56:21.572142+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14740","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: duox2 has been classified as Green List (High Evidence).","entity_name":"DUOX2","entity_type":"gene"},{"created":"2022-05-20T15:56:13.045655+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14740","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DUOX2 were changed from  to Thyroid dyshormonogenesis 6 - MIM#607200","entity_name":"DUOX2","entity_type":"gene"},{"created":"2022-05-20T15:55:52.363727+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14739","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DUOX2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DUOX2","entity_type":"gene"},{"created":"2022-05-20T15:44:55.918371+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14738","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: GDNF as ready","entity_name":"GDNF","entity_type":"gene"},{"created":"2022-05-20T15:44:55.902756+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14738","user_name":"Elena Savva","item_type":"entity","text":"Gene: gdnf has been classified as Red List (Low Evidence).","entity_name":"GDNF","entity_type":"gene"},{"created":"2022-05-20T15:41:26.369804+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14738","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DUOXA2 as ready","entity_name":"DUOXA2","entity_type":"gene"},{"created":"2022-05-20T15:41:26.355726+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14738","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: duoxa2 has been classified as Green List (High Evidence).","entity_name":"DUOXA2","entity_type":"gene"},{"created":"2022-05-20T15:41:17.600260+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14738","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DUOXA2 were changed from  to Thyroid dyshormonogenesis 5 - MIM#274900","entity_name":"DUOXA2","entity_type":"gene"},{"created":"2022-05-20T15:40:55.773196+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14737","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DUOXA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DUOXA2","entity_type":"gene"},{"created":"2022-05-20T15:39:54.470398+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ENPP1 as ready","entity_name":"ENPP1","entity_type":"gene"},{"created":"2022-05-20T15:39:54.457112+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: enpp1 has been classified as Green List (High Evidence).","entity_name":"ENPP1","entity_type":"gene"},{"created":"2022-05-20T15:39:20.437195+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPOR as ready","entity_name":"EPOR","entity_type":"gene"},{"created":"2022-05-20T15:39:20.424510+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epor has been classified as Green List (High Evidence).","entity_name":"EPOR","entity_type":"gene"},{"created":"2022-05-20T15:38:36.927177+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPRS as ready","entity_name":"EPRS","entity_type":"gene"},{"created":"2022-05-20T15:38:36.915133+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eprs has been classified as Green List (High Evidence).","entity_name":"EPRS","entity_type":"gene"},{"created":"2022-05-20T15:38:04.705167+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPS8 as ready","entity_name":"EPS8","entity_type":"gene"},{"created":"2022-05-20T15:38:04.690128+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eps8 has been classified as Green List (High Evidence).","entity_name":"EPS8","entity_type":"gene"},{"created":"2022-05-20T15:37:55.970618+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14736","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EPS8 were changed from  to Autosomal recessive nonsyndromic hearing loss 102 MONDO:0014428","entity_name":"EPS8","entity_type":"gene"},{"created":"2022-05-20T15:35:31.896521+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14735","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EPS8 were set to ","entity_name":"EPS8","entity_type":"gene"},{"created":"2022-05-20T15:35:11.686854+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14734","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EPS8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EPS8","entity_type":"gene"},{"created":"2022-05-20T15:34:20.665963+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14733","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ETFB as ready","entity_name":"ETFB","entity_type":"gene"},{"created":"2022-05-20T15:34:20.652577+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14733","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: etfb has been classified as Green List (High Evidence).","entity_name":"ETFB","entity_type":"gene"},{"created":"2022-05-20T15:34:11.019073+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14733","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ETFB were changed from  to multiple acyl-CoA dehydrogenase deficiency MONDO:0009282","entity_name":"ETFB","entity_type":"gene"},{"created":"2022-05-20T15:33:23.782940+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14732","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EXT1 as ready","entity_name":"EXT1","entity_type":"gene"},{"created":"2022-05-20T15:33:23.769541+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14732","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ext1 has been classified as Green List (High Evidence).","entity_name":"EXT1","entity_type":"gene"},{"created":"2022-05-20T15:33:10.894985+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14732","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EXT1 were changed from  to hereditary multiple osteochondromas MONDO:0005508; exostoses, multiple, type 1 MONDO:0007585","entity_name":"EXT1","entity_type":"gene"},{"created":"2022-05-20T15:32:27.373786+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14731","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EYA4 as ready","entity_name":"EYA4","entity_type":"gene"},{"created":"2022-05-20T15:32:27.360861+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14731","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eya4 has been classified as Green List (High Evidence).","entity_name":"EYA4","entity_type":"gene"},{"created":"2022-05-20T15:31:45.627443+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14731","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EYS as ready","entity_name":"EYS","entity_type":"gene"},{"created":"2022-05-20T15:31:45.612108+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14731","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eys has been classified as Green List (High Evidence).","entity_name":"EYS","entity_type":"gene"},{"created":"2022-05-20T15:31:33.610055+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14731","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EYS were changed from  to Retinitis pigmentosa 25 MONDO:0011272","entity_name":"EYS","entity_type":"gene"},{"created":"2022-05-20T15:31:10.604661+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14730","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EYS were set to ","entity_name":"EYS","entity_type":"gene"},{"created":"2022-05-20T15:30:35.367824+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14729","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EYS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EYS","entity_type":"gene"}]}