{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2064","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2062","results":[{"created":"2019-12-06T21:06:55.976531+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.748","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C19orf12 were changed from  to Neurodegeneration with brain iron accumulation 4, MIM#614298","entity_name":"C19orf12","entity_type":"gene"},{"created":"2019-12-06T21:06:41.869058+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.747","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C19orf12 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"C19orf12","entity_type":"gene"},{"created":"2019-12-06T21:06:33.958062+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.746","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: C19orf12 as Red List (low evidence)","entity_name":"C19orf12","entity_type":"gene"},{"created":"2019-12-06T21:06:33.950479+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.746","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c19orf12 has been classified as Red List (Low Evidence).","entity_name":"C19orf12","entity_type":"gene"},{"created":"2019-12-06T21:05:47.741254+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.745","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BSND as ready","entity_name":"BSND","entity_type":"gene"},{"created":"2019-12-06T21:05:47.733874+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.745","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bsnd has been classified as Green List (High Evidence).","entity_name":"BSND","entity_type":"gene"},{"created":"2019-12-06T21:05:37.973998+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.745","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BSND were changed from  to Bartter syndrome, type 4a, MIM#602522","entity_name":"BSND","entity_type":"gene"},{"created":"2019-12-06T21:05:17.377770+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.744","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BSND was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BSND","entity_type":"gene"},{"created":"2019-12-06T21:04:35.732820+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.743","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRAT1 as ready","entity_name":"BRAT1","entity_type":"gene"},{"created":"2019-12-06T21:04:35.725391+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.743","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brat1 has been classified as Green List (High Evidence).","entity_name":"BRAT1","entity_type":"gene"},{"created":"2019-12-06T21:04:28.643267+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.743","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRAT1 were changed from  to Neurodevelopmental disorder with cerebellar atrophy and with or without seizures, MIM#618056","entity_name":"BRAT1","entity_type":"gene"},{"created":"2019-12-06T21:04:16.354479+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.742","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BRAT1 were set to ","entity_name":"BRAT1","entity_type":"gene"},{"created":"2019-12-06T21:04:00.268229+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.741","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRAT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRAT1","entity_type":"gene"},{"created":"2019-12-06T21:03:31.679791+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.740","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BMPER as ready","entity_name":"BMPER","entity_type":"gene"},{"created":"2019-12-06T21:03:31.672807+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.740","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bmper has been classified as Green List (High Evidence).","entity_name":"BMPER","entity_type":"gene"},{"created":"2019-12-06T21:03:27.079431+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.740","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BMPER were changed from  to Diaphanospondylodysostosis, MIM#608022","entity_name":"BMPER","entity_type":"gene"},{"created":"2019-12-06T21:03:15.273849+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.739","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BMPER was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BMPER","entity_type":"gene"},{"created":"2019-12-06T21:02:37.904584+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.738","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BICD2 as ready","entity_name":"BICD2","entity_type":"gene"},{"created":"2019-12-06T21:02:37.897267+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.738","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bicd2 has been classified as Red List (Low Evidence).","entity_name":"BICD2","entity_type":"gene"},{"created":"2019-12-06T21:02:28.387596+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.738","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BICD2 were changed from  to Spinal muscular atrophy, lower extremity-predominant, 2A, autosomal dominant, MIM#615290","entity_name":"BICD2","entity_type":"gene"},{"created":"2019-12-06T21:02:16.330400+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.737","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BICD2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BICD2","entity_type":"gene"},{"created":"2019-12-06T21:01:57.728451+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.736","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BICD2 as Red List (low evidence)","entity_name":"BICD2","entity_type":"gene"},{"created":"2019-12-06T21:01:57.721520+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.736","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bicd2 has been classified as Red List (Low Evidence).","entity_name":"BICD2","entity_type":"gene"},{"created":"2019-12-06T21:01:01.483489+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.735","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BDNF as ready","entity_name":"BDNF","entity_type":"gene"},{"created":"2019-12-06T21:01:01.475885+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.735","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bdnf has been classified as Red List (Low Evidence).","entity_name":"BDNF","entity_type":"gene"},{"created":"2019-12-06T21:00:40.209331+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.735","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BDNF were changed from  to Central hypoventilation syndrome, congenital, MIM#209880","entity_name":"BDNF","entity_type":"gene"},{"created":"2019-12-06T21:00:23.486923+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.734","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BDNF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BDNF","entity_type":"gene"},{"created":"2019-12-06T21:00:13.941165+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BDNF as Red List (low evidence)","entity_name":"BDNF","entity_type":"gene"},{"created":"2019-12-06T21:00:13.932004+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bdnf has been classified as Red List (Low Evidence).","entity_name":"BDNF","entity_type":"gene"},{"created":"2019-12-06T20:59:41.986053+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.732","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBIP1 as ready","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-06T20:59:41.979053+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.732","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbip1 has been classified as Amber List (Moderate Evidence).","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-06T20:59:33.923597+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.732","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBIP1 were changed from  to Bardet-Biedl syndrome 18, MIM#615995","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-06T20:59:20.089620+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.731","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBIP1 were set to ","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-06T20:59:10.462396+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.730","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-06T20:58:54.362102+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.729","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BBIP1 as Amber List (moderate evidence)","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-06T20:58:54.354717+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.729","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbip1 has been classified as Amber List (Moderate Evidence).","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-06T20:58:19.146323+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.728","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B9D2 as ready","entity_name":"B9D2","entity_type":"gene"},{"created":"2019-12-06T20:58:19.139097+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.728","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b9d2 has been classified as Green List (High Evidence).","entity_name":"B9D2","entity_type":"gene"},{"created":"2019-12-06T20:58:01.529213+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.728","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B9D2 were changed from  to Joubert syndrome 34, MIM#614175; Meckel syndrome 10, MIM#614175","entity_name":"B9D2","entity_type":"gene"},{"created":"2019-12-06T20:57:47.300804+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.727","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B9D2 were set to ","entity_name":"B9D2","entity_type":"gene"},{"created":"2019-12-06T20:57:34.640629+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.726","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B9D2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B9D2","entity_type":"gene"},{"created":"2019-12-06T20:56:59.031685+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.725","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B9D1 as ready","entity_name":"B9D1","entity_type":"gene"},{"created":"2019-12-06T20:56:59.024503+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.725","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b9d1 has been classified as Green List (High Evidence).","entity_name":"B9D1","entity_type":"gene"},{"created":"2019-12-06T20:56:43.825668+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.725","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B9D1 were changed from  to Joubert syndrome 27, MIM#617120; Meckel syndrome 9, MIM#614209","entity_name":"B9D1","entity_type":"gene"},{"created":"2019-12-06T20:56:29.313261+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.724","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B9D1 were set to ","entity_name":"B9D1","entity_type":"gene"},{"created":"2019-12-06T20:56:14.413006+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.723","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B9D1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B9D1","entity_type":"gene"},{"created":"2019-12-06T20:16:24.616548+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.722","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B4GALT1 as ready","entity_name":"B4GALT1","entity_type":"gene"},{"created":"2019-12-06T20:16:24.609517+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.722","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4galt1 has been classified as Green List (High Evidence).","entity_name":"B4GALT1","entity_type":"gene"},{"created":"2019-12-06T20:16:18.685816+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.722","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B4GALT1 were changed from  to Congenital disorder of glycosylation, type Iid, MIM#607091","entity_name":"B4GALT1","entity_type":"gene"},{"created":"2019-12-06T20:16:05.088633+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.721","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GALT1 were set to ","entity_name":"B4GALT1","entity_type":"gene"},{"created":"2019-12-06T20:15:52.882289+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.720","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B4GALT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GALT1","entity_type":"gene"},{"created":"2019-12-06T20:15:14.958582+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.719","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B3GAT3 as ready","entity_name":"B3GAT3","entity_type":"gene"},{"created":"2019-12-06T20:15:14.950723+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.719","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b3gat3 has been classified as Red List (Low Evidence).","entity_name":"B3GAT3","entity_type":"gene"},{"created":"2019-12-06T20:15:10.356556+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.719","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B3GAT3 were changed from  to Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects, MIM#245600","entity_name":"B3GAT3","entity_type":"gene"},{"created":"2019-12-06T20:14:55.565525+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B3GAT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B3GAT3","entity_type":"gene"},{"created":"2019-12-06T20:14:48.098100+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.717","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B3GAT3 as Red List (low evidence)","entity_name":"B3GAT3","entity_type":"gene"},{"created":"2019-12-06T20:14:48.089964+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.717","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b3gat3 has been classified as Red List (Low Evidence).","entity_name":"B3GAT3","entity_type":"gene"},{"created":"2019-12-06T20:13:57.284355+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.716","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B3GALT6 as ready","entity_name":"B3GALT6","entity_type":"gene"},{"created":"2019-12-06T20:13:57.276673+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.716","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b3galt6 has been classified as Amber List (Moderate Evidence).","entity_name":"B3GALT6","entity_type":"gene"},{"created":"2019-12-06T20:08:04.093704+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.716","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B3GALT6 were changed from  to Ehlers-Danlos syndrome, spondylodysplastic type, 2, MIM#615349; Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures, MIM#271640","entity_name":"B3GALT6","entity_type":"gene"},{"created":"2019-12-06T20:07:52.413554+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B3GALT6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B3GALT6","entity_type":"gene"},{"created":"2019-12-06T20:07:30.645587+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.714","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: B3GALT6 as Amber List (moderate evidence)","entity_name":"B3GALT6","entity_type":"gene"},{"created":"2019-12-06T20:07:30.637894+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.714","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b3galt6 has been classified as Amber List (Moderate Evidence).","entity_name":"B3GALT6","entity_type":"gene"},{"created":"2019-12-06T20:06:28.792414+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.713","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AHCY as ready","entity_name":"AHCY","entity_type":"gene"},{"created":"2019-12-06T20:06:28.785223+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.713","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ahcy has been classified as Green List (High Evidence).","entity_name":"AHCY","entity_type":"gene"},{"created":"2019-12-06T20:06:24.582894+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.713","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AHCY were changed from  to Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase, MIM#613752","entity_name":"AHCY","entity_type":"gene"},{"created":"2019-12-06T20:06:11.649149+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.712","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AHCY was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"AHCY","entity_type":"gene"},{"created":"2019-12-06T20:00:56.258255+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.711","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ASNS as ready","entity_name":"ASNS","entity_type":"gene"},{"created":"2019-12-06T20:00:56.251220+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.711","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: asns has been classified as Green List (High Evidence).","entity_name":"ASNS","entity_type":"gene"},{"created":"2019-12-06T20:00:46.570257+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.711","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ASNS were changed from  to Asparagine synthetase deficiency, MIM#615574","entity_name":"ASNS","entity_type":"gene"},{"created":"2019-12-06T20:00:09.822329+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.710","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ASL as ready","entity_name":"ASL","entity_type":"gene"},{"created":"2019-12-06T20:00:09.813755+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.710","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: asl has been classified as Green List (High Evidence).","entity_name":"ASL","entity_type":"gene"},{"created":"2019-12-06T20:00:04.973780+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.710","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ASL were changed from  to Argininosuccinic aciduria, MIM#207900","entity_name":"ASL","entity_type":"gene"},{"created":"2019-12-06T19:59:52.332297+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.709","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ASL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ASL","entity_type":"gene"},{"created":"2019-12-06T19:58:52.525920+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALX3 as ready","entity_name":"ALX3","entity_type":"gene"},{"created":"2019-12-06T19:58:52.518528+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alx3 has been classified as Green List (High Evidence).","entity_name":"ALX3","entity_type":"gene"},{"created":"2019-12-06T19:58:48.378610+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.708","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALX3 were changed from  to Frontonasal dysplasia 1, MIM#136760","entity_name":"ALX3","entity_type":"gene"},{"created":"2019-12-06T19:58:35.365407+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.707","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALX3 were set to ","entity_name":"ALX3","entity_type":"gene"},{"created":"2019-12-06T19:58:23.193269+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.706","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALX3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALX3","entity_type":"gene"},{"created":"2019-12-06T19:57:52.090231+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.705","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALX1 as ready","entity_name":"ALX1","entity_type":"gene"},{"created":"2019-12-06T19:57:52.083045+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.705","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alx1 has been classified as Amber List (Moderate Evidence).","entity_name":"ALX1","entity_type":"gene"},{"created":"2019-12-06T19:57:45.234868+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.705","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALX1 were changed from  to Frontonasal dysplasia 3, MIM#613456","entity_name":"ALX1","entity_type":"gene"},{"created":"2019-12-06T19:57:31.470551+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.704","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALX1 were set to ","entity_name":"ALX1","entity_type":"gene"},{"created":"2019-12-06T19:57:18.837105+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.703","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALX1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALX1","entity_type":"gene"},{"created":"2019-12-06T19:57:03.580665+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.702","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ALX1 as Amber List (moderate evidence)","entity_name":"ALX1","entity_type":"gene"},{"created":"2019-12-06T19:57:03.573447+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.702","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alx1 has been classified as Amber List (Moderate Evidence).","entity_name":"ALX1","entity_type":"gene"},{"created":"2019-12-06T19:56:32.061130+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.701","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALG14 as ready","entity_name":"ALG14","entity_type":"gene"},{"created":"2019-12-06T19:56:32.054150+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.701","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alg14 has been classified as Green List (High Evidence).","entity_name":"ALG14","entity_type":"gene"},{"created":"2019-12-06T19:56:26.974710+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.701","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALG14 were changed from  to Myasthenic syndrome, congenital, 15, without tubular aggregates, MIM#616227; Intellectual disability","entity_name":"ALG14","entity_type":"gene"},{"created":"2019-12-06T19:56:14.342048+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.700","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALG14 were set to ","entity_name":"ALG14","entity_type":"gene"},{"created":"2019-12-06T19:56:00.000356+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.699","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALG14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALG14","entity_type":"gene"},{"created":"2019-12-06T19:55:15.184906+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALDOB as ready","entity_name":"ALDOB","entity_type":"gene"},{"created":"2019-12-06T19:55:15.177759+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aldob has been classified as Green List (High Evidence).","entity_name":"ALDOB","entity_type":"gene"},{"created":"2019-12-06T19:55:04.495445+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.698","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALDOB were changed from  to Fructose intolerance, hereditary, MIM#229600","entity_name":"ALDOB","entity_type":"gene"},{"created":"2019-12-06T19:54:52.460710+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.697","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALDOB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALDOB","entity_type":"gene"},{"created":"2019-12-06T19:53:29.709872+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.696","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AGA as ready","entity_name":"AGA","entity_type":"gene"},{"created":"2019-12-06T19:53:29.702842+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.696","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aga has been classified as Green List (High Evidence).","entity_name":"AGA","entity_type":"gene"},{"created":"2019-12-06T19:53:25.328517+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.696","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AGA were changed from  to Aspartylglucosaminuria, MIM#208400","entity_name":"AGA","entity_type":"gene"},{"created":"2019-12-06T19:53:11.584984+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.695","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AGA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"AGA","entity_type":"gene"},{"created":"2019-12-06T19:52:33.934718+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.694","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADD3 as ready","entity_name":"ADD3","entity_type":"gene"}]}