{"count":221416,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=409","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=407","results":[{"created":"2024-08-08T14:41:09.642274+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.134","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: WNT1 as ready","entity_name":"WNT1","entity_type":"gene"},{"created":"2024-08-08T14:41:09.620791+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.134","user_name":"Lilian Downie","item_type":"entity","text":"Gene: wnt1 has been classified as Green List (High Evidence).","entity_name":"WNT1","entity_type":"gene"},{"created":"2024-08-08T14:41:03.945168+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.134","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: WNT1 were set to ","entity_name":"WNT1","entity_type":"gene"},{"created":"2024-08-08T14:39:45.027627+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.133","user_name":"Lilian Downie","item_type":"entity","text":"Phenotypes for gene: COX20 were changed from Mitochondrial complex IV deficiency, 220110 (3) to Mitochondrial complex IV deficiency, nuclear type 11, MIM#619054","entity_name":"COX20","entity_type":"gene"},{"created":"2024-08-08T14:39:07.903252+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.132","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: COX20 as ready","entity_name":"COX20","entity_type":"gene"},{"created":"2024-08-08T14:39:07.892849+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.132","user_name":"Lilian Downie","item_type":"entity","text":"Gene: cox20 has been classified as Green List (High Evidence).","entity_name":"COX20","entity_type":"gene"},{"created":"2024-08-08T14:39:01.368386+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.132","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: COX20 were set to ","entity_name":"COX20","entity_type":"gene"},{"created":"2024-08-08T14:38:04.464792+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.131","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CPT2 as ready","entity_name":"CPT2","entity_type":"gene"},{"created":"2024-08-08T14:38:04.455219+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.131","user_name":"Lilian Downie","item_type":"entity","text":"Gene: cpt2 has been classified as Green List (High Evidence).","entity_name":"CPT2","entity_type":"gene"},{"created":"2024-08-08T14:38:00.723716+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.131","user_name":"Lilian Downie","item_type":"entity","text":"Phenotypes for gene: CPT2 were changed from CPT II deficiency, lethal neonatal, 608836 (3) to CPT II deficiency, infantile MIM#600649; CPT II deficiency, lethal neonatal MIM#608836; CPT II deficiency, myopathic, stress-induced MIM#255110","entity_name":"CPT2","entity_type":"gene"},{"created":"2024-08-08T14:37:45.053399+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.130","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CPT2 were set to ","entity_name":"CPT2","entity_type":"gene"},{"created":"2024-08-08T14:36:34.079815+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.129","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: DHODH as ready","entity_name":"DHODH","entity_type":"gene"},{"created":"2024-08-08T14:36:34.063789+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.129","user_name":"Lilian Downie","item_type":"entity","text":"Gene: dhodh has been classified as Green List (High Evidence).","entity_name":"DHODH","entity_type":"gene"},{"created":"2024-08-08T14:36:29.692957+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.129","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: DHODH were set to ","entity_name":"DHODH","entity_type":"gene"},{"created":"2024-08-08T14:34:21.479528+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.128","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: ACADM as ready","entity_name":"ACADM","entity_type":"gene"},{"created":"2024-08-08T14:34:21.458922+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.128","user_name":"Lilian Downie","item_type":"entity","text":"Gene: acadm has been classified as Green List (High Evidence).","entity_name":"ACADM","entity_type":"gene"},{"created":"2024-08-08T14:34:14.157183+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.128","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: ACADM were set to ","entity_name":"ACADM","entity_type":"gene"},{"created":"2024-08-08T14:30:23.980686+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.127","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: ERCC6L2 as ready","entity_name":"ERCC6L2","entity_type":"gene"},{"created":"2024-08-08T14:30:23.958854+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.127","user_name":"Lilian Downie","item_type":"entity","text":"Gene: ercc6l2 has been classified as Green List (High Evidence).","entity_name":"ERCC6L2","entity_type":"gene"},{"created":"2024-08-08T14:30:18.349770+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.127","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: ERCC6L2 were set to ","entity_name":"ERCC6L2","entity_type":"gene"},{"created":"2024-08-08T14:29:32.410187+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.42","user_name":"Zornitza Stark","item_type":"panel","text":"List of related panels changed from Seizure; HP:0001250 to Seizure; HP:0001250; Epileptic encephalopathy; HP:0200134","entity_name":null,"entity_type":null},{"created":"2024-08-08T14:14:54.488347+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.126","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: ADAT3 as ready","entity_name":"ADAT3","entity_type":"gene"},{"created":"2024-08-08T14:14:54.466799+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.126","user_name":"Lilian Downie","item_type":"entity","text":"Gene: adat3 has been classified as Green List (High Evidence).","entity_name":"ADAT3","entity_type":"gene"},{"created":"2024-08-08T14:14:50.490356+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.126","user_name":"Lilian Downie","item_type":"entity","text":"Phenotypes for gene: ADAT3 were changed from Mental retardation, autosomal recessive 36, 615286 (3) to Neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies, MIM#615286","entity_name":"ADAT3","entity_type":"gene"},{"created":"2024-08-08T14:14:37.066838+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.125","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: ADAT3 were set to ","entity_name":"ADAT3","entity_type":"gene"},{"created":"2024-08-08T14:07:17.614958+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.124","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: CYP11A1 as ready","entity_name":"CYP11A1","entity_type":"gene"},{"created":"2024-08-08T14:07:17.604215+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.124","user_name":"Lilian Downie","item_type":"entity","text":"Gene: cyp11a1 has been classified as Green List (High Evidence).","entity_name":"CYP11A1","entity_type":"gene"},{"created":"2024-08-08T14:07:13.351812+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.124","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: CYP11A1 were set to ","entity_name":"CYP11A1","entity_type":"gene"},{"created":"2024-08-08T14:04:58.366631+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.123","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: ARMC4 as ready","entity_name":"ARMC4","entity_type":"gene"},{"created":"2024-08-08T14:04:58.358542+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.123","user_name":"Lilian Downie","item_type":"entity","text":"Added comment: Comment when marking as ready: Primary ciliary dyskinesia-23 is an autosomal recessive disorder resulting from defective ciliary motility. Affected individuals have respiratory distress and recurrent upper and lower airway infections, and they often develop bronchiectasis. About 50% of patients have situs inversus or laterality defects. Ultrastructural analysis of respiratory cilia shows defects in the outer dynein arm","entity_name":"ARMC4","entity_type":"gene"},{"created":"2024-08-08T14:04:58.282233+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.123","user_name":"Lilian Downie","item_type":"entity","text":"Gene: armc4 has been classified as Green List (High Evidence).","entity_name":"ARMC4","entity_type":"gene"},{"created":"2024-08-08T14:04:53.765917+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.123","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: ARMC4 were set to ","entity_name":"ARMC4","entity_type":"gene"},{"created":"2024-08-08T14:01:39.286187+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.122","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: ARV1 as ready","entity_name":"ARV1","entity_type":"gene"},{"created":"2024-08-08T14:01:39.281828+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.122","user_name":"Lilian Downie","item_type":"entity","text":"Added comment: Comment when marking as ready: Developmental and epileptic encephalopathy-38 (DEE38) is an autosomal recessive neurologic and neurodegenerative disorder characterized by the onset of various type of seizures usually between about 4 and 7 months of age. Prior to the onset of seizures, most infants show severely impaired global development, hypotonia with poor head control, and visual inattention with roving eye movements and nystagmus. Seizures are usually refractory to treatment and associated with status epilepticus. Patients have little or no development with inability to walk or speak, spasticity or abnormal movements, and often cortical blindness. There is failure to thrive, and many require tube-feeding. Death in early childhood due to aspiration or intractable epilepsy may occur.","entity_name":"ARV1","entity_type":"gene"},{"created":"2024-08-08T14:01:39.237127+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.122","user_name":"Lilian Downie","item_type":"entity","text":"Gene: arv1 has been classified as Green List (High Evidence).","entity_name":"ARV1","entity_type":"gene"},{"created":"2024-08-08T13:05:04.691634+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.122","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BUB1B as ready","entity_name":"BUB1B","entity_type":"gene"},{"created":"2024-08-08T13:05:04.678744+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.122","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bub1b has been classified as Green List (High Evidence).","entity_name":"BUB1B","entity_type":"gene"},{"created":"2024-08-08T13:04:59.924816+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.122","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BUB1B were changed from Mosaic variegated aneuploidy syndrome 1, 257300 (3) to Mosaic variegated aneuploidy syndrome 1, MIM# 257300","entity_name":"BUB1B","entity_type":"gene"},{"created":"2024-08-08T13:04:39.027776+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.121","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BUB1B were set to ","entity_name":"BUB1B","entity_type":"gene"},{"created":"2024-08-08T13:03:57.066147+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.120","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C12orf57 as ready","entity_name":"C12orf57","entity_type":"gene"},{"created":"2024-08-08T13:03:57.053146+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.120","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c12orf57 has been classified as Green List (High Evidence).","entity_name":"C12orf57","entity_type":"gene"},{"created":"2024-08-08T13:03:53.768302+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.120","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C12orf57 were changed from Temtamy syndrome, 218340 (3) to Temtamy syndrome, MIM # 218340","entity_name":"C12orf57","entity_type":"gene"},{"created":"2024-08-08T13:03:41.335572+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.119","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C12orf57 were set to ","entity_name":"C12orf57","entity_type":"gene"},{"created":"2024-08-08T13:03:04.227447+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.118","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: C12orf57.","entity_name":"C12orf57","entity_type":"gene"},{"created":"2024-08-08T13:02:27.540742+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.118","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHST3 as ready","entity_name":"CHST3","entity_type":"gene"},{"created":"2024-08-08T13:02:27.508880+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.118","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chst3 has been classified as Green List (High Evidence).","entity_name":"CHST3","entity_type":"gene"},{"created":"2024-08-08T13:02:23.732068+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.118","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CHST3 were set to ","entity_name":"CHST3","entity_type":"gene"},{"created":"2024-08-08T12:58:53.964477+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.117","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CNTNAP1 as ready","entity_name":"CNTNAP1","entity_type":"gene"},{"created":"2024-08-08T12:58:53.950792+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.117","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cntnap1 has been classified as Green List (High Evidence).","entity_name":"CNTNAP1","entity_type":"gene"},{"created":"2024-08-08T12:58:48.573560+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.117","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CNTNAP1 were changed from Lethal congenital contracture syndrome 7, 616286 (3) to Lethal congenital contracture syndrome 7, MIM # 616286; Hypomyelinating neuropathy, congenital, 3, MIM # 618186","entity_name":"CNTNAP1","entity_type":"gene"},{"created":"2024-08-08T12:58:30.506182+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.116","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CNTNAP1 were set to ","entity_name":"CNTNAP1","entity_type":"gene"},{"created":"2024-08-08T12:57:55.594685+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.115","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COG7 as ready","entity_name":"COG7","entity_type":"gene"},{"created":"2024-08-08T12:57:55.560125+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.115","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cog7 has been classified as Green List (High Evidence).","entity_name":"COG7","entity_type":"gene"},{"created":"2024-08-08T12:57:52.285132+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.115","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COG7 were changed from Congenital disorder of glycosylation, type IIe, 608779 (3) to Congenital disorder of glycosylation, type IIe, MIM # 608779","entity_name":"COG7","entity_type":"gene"},{"created":"2024-08-08T12:57:39.545591+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.114","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COG7 were set to ","entity_name":"COG7","entity_type":"gene"},{"created":"2024-08-08T12:56:55.104281+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYP17A1 as ready","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2024-08-08T12:56:55.086946+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp17a1 has been classified as Green List (High Evidence).","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2024-08-08T12:56:47.848450+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CYP17A1 were changed from 17,20-lyase deficiency, isolated, 202110 (3) to 17-alpha-hydroxylase/17,20-lyase deficiency MIM#202110","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2024-08-08T12:56:35.915063+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.112","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CYP17A1 were set to ","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2024-08-08T12:55:59.526639+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.111","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYP2U1 as ready","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2024-08-08T12:55:59.511620+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.111","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp2u1 has been classified as Green List (High Evidence).","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2024-08-08T12:55:43.313064+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.111","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CYP2U1 were changed from Spastic paraplegia 56, autosomal recessive, 615030 (3) to Spastic paraplegia 56, autosomal recessive MIM#615030","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2024-08-08T12:55:30.384891+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.110","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CYP2U1 were set to ","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2024-08-08T12:54:52.326491+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.109","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCX as ready","entity_name":"DCX","entity_type":"gene"},{"created":"2024-08-08T12:54:52.304299+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.109","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcx has been classified as Green List (High Evidence).","entity_name":"DCX","entity_type":"gene"},{"created":"2024-08-08T12:54:48.122342+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.109","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DCX were changed from Lissencephaly, X-linked, 300067 (3) to Lissencephaly, X-linked MIM#300067; Subcortical laminal heterotopia, X-linked MIM#300067","entity_name":"DCX","entity_type":"gene"},{"created":"2024-08-08T12:54:35.335388+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.108","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DCX were set to ","entity_name":"DCX","entity_type":"gene"},{"created":"2024-08-08T12:53:47.217618+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.107","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDX59 as ready","entity_name":"DDX59","entity_type":"gene"},{"created":"2024-08-08T12:53:47.194123+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.107","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddx59 has been classified as Green List (High Evidence).","entity_name":"DDX59","entity_type":"gene"},{"created":"2024-08-08T12:53:43.249879+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.107","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DDX59 were set to ","entity_name":"DDX59","entity_type":"gene"},{"created":"2024-08-08T12:53:08.601739+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.106","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2AK3 as ready","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2024-08-08T12:53:08.555938+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.106","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2ak3 has been classified as Green List (High Evidence).","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2024-08-08T12:53:03.217723+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.106","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2AK3 were changed from Wolcott-Rallison syndrome, 226980 (3) to Wolcott-Rallison syndrome MIM#226980","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2024-08-08T12:52:52.033573+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.105","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EIF2AK3 were set to ","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2024-08-08T12:52:06.952058+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.104","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ASPM as ready","entity_name":"ASPM","entity_type":"gene"},{"created":"2024-08-08T12:52:06.912847+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.104","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aspm has been classified as Green List (High Evidence).","entity_name":"ASPM","entity_type":"gene"},{"created":"2024-08-08T12:52:01.456098+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.104","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ASPM were changed from Microcephaly 5, primary, autosomal recessive, 608716 (3) to Microcephaly 5, primary, autosomal recessive (MIM#608716)","entity_name":"ASPM","entity_type":"gene"},{"created":"2024-08-08T12:51:44.796379+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.103","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ASPM were set to ","entity_name":"ASPM","entity_type":"gene"},{"created":"2024-08-08T12:51:10.576662+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.102","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATP7A as ready","entity_name":"ATP7A","entity_type":"gene"},{"created":"2024-08-08T12:51:10.552172+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.102","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp7a has been classified as Green List (High Evidence).","entity_name":"ATP7A","entity_type":"gene"},{"created":"2024-08-08T12:51:05.804584+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.102","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATP7A were changed from Menkes disease, 309400 (3) to Menkes disease(MIM#309400); Occipital horn syndrome(MIM#304150)","entity_name":"ATP7A","entity_type":"gene"},{"created":"2024-08-08T12:50:52.875940+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.101","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATP7A were set to ","entity_name":"ATP7A","entity_type":"gene"},{"created":"2024-08-08T12:50:22.339095+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.100","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADAMTS2 as ready","entity_name":"ADAMTS2","entity_type":"gene"},{"created":"2024-08-08T12:50:22.326515+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.100","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adamts2 has been classified as Green List (High Evidence).","entity_name":"ADAMTS2","entity_type":"gene"},{"created":"2024-08-08T12:50:17.910620+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.100","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADAMTS2 were changed from Ehlers-Danlos syndrome, type VIIC, 225410 (3) to Ehlers-Danlos syndrome, dermatosparaxis type (MIM# 225410)","entity_name":"ADAMTS2","entity_type":"gene"},{"created":"2024-08-08T12:50:00.778130+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.99","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ADAMTS2 were set to ","entity_name":"ADAMTS2","entity_type":"gene"},{"created":"2024-08-08T12:49:46.624997+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.98","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Congenital onset, severe CTD.; to: Congenital onset, marked joint hyper mobility, skin abnormalities, risk of organ rupture.","entity_name":"ADAMTS2","entity_type":"gene"},{"created":"2024-08-08T12:48:51.571694+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.98","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ADAMTS2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ehlers-Danlos syndrome, dermatosparaxis type (MIM# 225410); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADAMTS2","entity_type":"gene"},{"created":"2024-08-08T12:42:39.052600+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AGRN as ready","entity_name":"AGRN","entity_type":"gene"},{"created":"2024-08-08T12:42:39.040971+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: agrn has been classified as Green List (High Evidence).","entity_name":"AGRN","entity_type":"gene"},{"created":"2024-08-08T12:42:34.368393+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.98","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AGRN were set to ","entity_name":"AGRN","entity_type":"gene"},{"created":"2024-08-08T12:41:59.975142+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.97","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARSA as ready","entity_name":"ARSA","entity_type":"gene"},{"created":"2024-08-08T12:41:59.961570+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.97","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arsa has been classified as Green List (High Evidence).","entity_name":"ARSA","entity_type":"gene"},{"created":"2024-08-08T12:41:42.020947+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.97","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ARSA were set to ","entity_name":"ARSA","entity_type":"gene"},{"created":"2024-08-08T12:41:17.333478+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.96","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATAD1 as ready","entity_name":"ATAD1","entity_type":"gene"},{"created":"2024-08-08T12:41:17.322927+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atad1 has been classified as Green List (High Evidence).","entity_name":"ATAD1","entity_type":"gene"},{"created":"2024-08-08T12:35:01.226840+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.96","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATAD1 were changed from Hyperekplexia 4, 618011 (3), Autosomal recessive to Hyperekplexia 4, MIM#618011","entity_name":"ATAD1","entity_type":"gene"},{"created":"2024-08-08T12:34:50.661246+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.95","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATAD1 were set to ","entity_name":"ATAD1","entity_type":"gene"},{"created":"2024-08-08T12:34:12.224568+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.94","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATR as ready","entity_name":"ATR","entity_type":"gene"},{"created":"2024-08-08T12:34:12.201782+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atr has been classified as Green List (High Evidence).","entity_name":"ATR","entity_type":"gene"}]}