{"count":220828,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1977","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1975","results":[{"created":"2020-01-17T16:54:10.966032+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1619","user_name":"Alison Yeung","item_type":"entity","text":"gene: KCNN3 was added\ngene: KCNN3 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: KCNN3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: KCNN3 were set to PMID: 31155282\nPhenotypes for gene: KCNN3 were set to Zimmermann-Laband syndrome 3; OMIM# 618658\nReview for gene: KCNN3 was set to GREEN\ngene: KCNN3 was marked as current diagnostic\nAdded comment: Reported in three unrelated individuals \nSources: Literature","entity_name":"KCNN3","entity_type":"gene"},{"created":"2020-01-17T16:47:56.985406+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNND2 as ready","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:47:56.974159+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnd2 has been classified as Amber List (Moderate Evidence).","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:47:49.341265+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTNND2 as Amber List (moderate evidence)","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:47:49.330172+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnd2 has been classified as Amber List (Moderate Evidence).","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:47:11.235286+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.843","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNND2 as ready","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:47:11.222342+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.843","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnd2 has been classified as Amber List (Moderate Evidence).","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:46:49.477981+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.843","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNND2 were changed from  to Intellectual disability; Autism; Epilepsy","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:46:27.994372+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.842","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNND2 were set to ","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:46:01.485433+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.841","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNND2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:45:32.823310+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.840","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTNND2 as Amber List (moderate evidence)","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:45:32.811642+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.840","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnd2 has been classified as Amber List (Moderate Evidence).","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:45:25.417155+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNND2 were changed from  to Intellectual disability; Autism; Epilepsy","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:45:07.537637+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.839","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTNND2: Rating: AMBER; Mode of pathogenicity: None; Publications: 25839933, 29127138, 25807484; Phenotypes: Intellectual disability, Autism, Epilepsy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:44:50.622212+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNND2 were set to ","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:44:22.775016+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNND2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:43:11.033515+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTNND2: Rating: AMBER; Mode of pathogenicity: None; Publications: 25839933, 29127138, 25807484; Phenotypes: Intellectual disability, Autism, Epilepsy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:41:55.575362+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.839","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADCY8 as ready","entity_name":"ADCY8","entity_type":"gene"},{"created":"2020-01-17T16:41:55.569941+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.839","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Cannot find evidence for Mendelian gene-disease association.","entity_name":"ADCY8","entity_type":"gene"},{"created":"2020-01-17T16:41:55.528021+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.839","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy8 has been classified as Red List (Low Evidence).","entity_name":"ADCY8","entity_type":"gene"},{"created":"2020-01-17T16:41:50.952070+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1618","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNND2 as ready","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:41:50.940643+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1618","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnd2 has been classified as Amber List (Moderate Evidence).","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:41:40.492840+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1618","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNND2 were changed from Intellectual disability; Autism; Epilepsy to Intellectual disability; Autism; Epilepsy","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:41:32.380947+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.839","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADCY8 as Red List (low evidence)","entity_name":"ADCY8","entity_type":"gene"},{"created":"2020-01-17T16:41:32.367901+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.839","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy8 has been classified as Red List (Low Evidence).","entity_name":"ADCY8","entity_type":"gene"},{"created":"2020-01-17T16:41:08.071897+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1618","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNND2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:40:34.634206+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1617","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNND2 were changed from  to Intellectual disability; Autism; Epilepsy","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:40:09.121069+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.8","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: CNOT1 as ready","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:40:08.473468+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.8","user_name":"Alison Yeung","item_type":"entity","text":"Gene: cnot1 has been classified as Green List (High Evidence).","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:40:05.287157+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1617","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNND2 were set to ","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:39:54.453727+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.8","user_name":"Alison Yeung","item_type":"entity","text":"Classified gene: CNOT1 as Green List (high evidence)","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:39:54.440526+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.8","user_name":"Alison Yeung","item_type":"entity","text":"Gene: cnot1 has been classified as Green List (High Evidence).","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:39:19.657075+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1616","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTNND2 as Amber List (moderate evidence)","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:39:18.974011+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1616","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnd2 has been classified as Amber List (Moderate Evidence).","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:38:31.164645+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1615","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTNND2: Rating: AMBER; Mode of pathogenicity: None; Publications: 25839933, 29127138, 25807484; Phenotypes: Intellectual disability, Autism, Epilepsy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNND2","entity_type":"gene"},{"created":"2020-01-17T16:29:17.976884+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.7","user_name":"Alison Yeung","item_type":"entity","text":"gene: CNOT1 was added\ngene: CNOT1 was added to Holoprosencephaly and septo-optic dysplasia. Sources: Literature\nMode of inheritance for gene: CNOT1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: CNOT1 were set to PMID: 31006513\nPhenotypes for gene: CNOT1 were set to HOLOPROSENCEPHALY 12 WITH OR WITHOUT PANCREATIC AGENESIS; HPE12; OMIM# 618500\nReview for gene: CNOT1 was set to GREEN\ngene: CNOT1 was marked as current diagnostic\nAdded comment: Three unrelated individuals reported. Functional studies in mouse \nSources: Literature","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:26:56.641237+11:00","panel_name":"Hereditary Haemorrhagic Telangiectasia","panel_id":260,"panel_version":"0.6","user_name":"Bryony Thompson","item_type":"panel","text":"Panel types changed to Royal Melbourne Hospital; Rare Disease","entity_name":null,"entity_type":null},{"created":"2020-01-17T16:21:32.933249+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.838","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: CNOT1 as ready","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:21:32.921565+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.838","user_name":"Alison Yeung","item_type":"entity","text":"Gene: cnot1 has been classified as Green List (High Evidence).","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:21:24.088462+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.838","user_name":"Alison Yeung","item_type":"entity","text":"Classified gene: CNOT1 as Green List (high evidence)","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:21:24.076921+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.838","user_name":"Alison Yeung","item_type":"entity","text":"Gene: cnot1 has been classified as Green List (High Evidence).","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T16:21:02.105133+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.837","user_name":"Alison Yeung","item_type":"entity","text":"gene: CNOT1 was added\ngene: CNOT1 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: CNOT1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: CNOT1 were set to PMID: 31006513\nPhenotypes for gene: CNOT1 were set to Holoprosencephaly 12, with or without pancreatic agenesis; OMIM# 618500\nReview for gene: CNOT1 was set to GREEN\ngene: CNOT1 was marked as current diagnostic\nAdded comment: Reported in 3 unrelated individuals \nSources: Literature","entity_name":"CNOT1","entity_type":"gene"},{"created":"2020-01-17T15:55:28.379352+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.836","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IQSEC1 as ready","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:55:28.367606+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.836","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqsec1 has been classified as Green List (High Evidence).","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:55:19.295121+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.836","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IQSEC1 as Green List (high evidence)","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:55:19.283637+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.836","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqsec1 has been classified as Green List (High Evidence).","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:55:02.474991+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.835","user_name":"Zornitza Stark","item_type":"entity","text":"gene: IQSEC1 was added\ngene: IQSEC1 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: IQSEC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: IQSEC1 were set to 31607425\nPhenotypes for gene: IQSEC1 were set to Intellectual developmental disorder with short stature and behavioral abnormalities, MIM#\t618687\nReview for gene: IQSEC1 was set to GREEN\nAdded comment: Five individuals from two unrelated families reported, animal model data. \nSources: Literature","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:54:51.603618+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1615","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IQSEC1 as ready","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:54:51.592389+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1615","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqsec1 has been classified as Green List (High Evidence).","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:54:27.038545+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1615","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IQSEC1 as Green List (high evidence)","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:54:27.026921+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1615","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iqsec1 has been classified as Green List (High Evidence).","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:53:19.467950+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.1614","user_name":"Zornitza Stark","item_type":"entity","text":"gene: IQSEC1 was added\ngene: IQSEC1 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: IQSEC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: IQSEC1 were set to 31607425\nPhenotypes for gene: IQSEC1 were set to Intellectual developmental disorder with short stature and behavioral abnormalities, MIM#\t618687\nReview for gene: IQSEC1 was set to GREEN\nAdded comment: Five individuals from two unrelated families reported, animal model data. \nSources: Literature","entity_name":"IQSEC1","entity_type":"gene"},{"created":"2020-01-17T15:00:48.962887+11:00","panel_name":"Hereditary Haemorrhagic Telangiectasia","panel_id":260,"panel_version":"0.5","user_name":"Bryony Thompson","item_type":"panel","text":"Panel name changed from Hereditary Haemorrhagic Telangiectasia_RMH to Hereditary Haemorrhagic Telangiectasia\nPanel types changed to Royal Melbourne Hospital","entity_name":null,"entity_type":null},{"created":"2020-01-17T14:56:38.417544+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNJ11 as ready","entity_name":"KCNJ11","entity_type":"gene"},{"created":"2020-01-17T14:56:38.404957+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnj11 has been classified as Green List (High Evidence).","entity_name":"KCNJ11","entity_type":"gene"},{"created":"2020-01-17T14:52:24.615768+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.834","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACAN as ready","entity_name":"ACAN","entity_type":"gene"},{"created":"2020-01-17T14:52:24.604234+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.834","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acan has been classified as Green List (High Evidence).","entity_name":"ACAN","entity_type":"gene"},{"created":"2020-01-17T14:52:12.563143+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.834","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACAN as Green List (high evidence)","entity_name":"ACAN","entity_type":"gene"},{"created":"2020-01-17T14:52:12.551284+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.834","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acan has been classified as Green List (High Evidence).","entity_name":"ACAN","entity_type":"gene"},{"created":"2020-01-17T14:51:53.502480+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.833","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ACAN was added\ngene: ACAN was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: ACAN was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: ACAN were set to Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans, OMIM#\t165800; Spondyloepimetaphyseal dysplasia, aggrecan type\t612813\nReview for gene: ACAN was set to GREEN\nAdded comment: Sources: Expert list","entity_name":"ACAN","entity_type":"gene"},{"created":"2020-01-17T14:34:29.547942+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.832","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NKX2-2 as ready","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:34:29.536507+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.832","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx2-2 has been classified as Green List (High Evidence).","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:34:12.000578+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.832","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NKX2-2 as Green List (high evidence)","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:34:11.988186+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.832","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx2-2 has been classified as Green List (High Evidence).","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:33:53.890187+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.831","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NKX2-2 was added\ngene: NKX2-2 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: NKX2-2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NKX2-2 were set to 24411943; 9584121\nPhenotypes for gene: NKX2-2 were set to Syndromic neonatal diabetes, with severe developmental delay, hypotonia, cortical blindness, hearing impairment\nReview for gene: NKX2-2 was set to GREEN\nAdded comment: Sources: Expert list","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:31:38.425741+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NKX2-2 as ready","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:31:38.420317+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Mouse model also supports gene-disease association.","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:31:38.390865+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx2-2 has been classified as Green List (High Evidence).","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:31:30.514666+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NKX2-2 were set to 24411943","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:30:39.984090+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NKX2-2 were changed from  to Syndromic neonatal diabetes, with severe developmental delay, hypotonia, cortical blindness, hearing impairment","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:30:26.405601+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NKX2-2: Rating: GREEN; Mode of pathogenicity: None; Publications: 24411943; Phenotypes: Syndromic neonatal diabetes, with severe developmental delay, hypotonia, cortical blindness, hearing impairment; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:23:18.985760+11:00","panel_name":"Monogenic Diabetes","panel_id":3093,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Monogenic diabetes to Monogenic Diabetes\nPanel types changed to Rare Disease; Victorian Clinical Genetics Services","entity_name":null,"entity_type":null},{"created":"2020-01-17T14:20:18.549933+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZMPSTE24 was added\ngene: ZMPSTE24 was added to Monogenic diabetes. Sources: Expert Review Green\nMode of inheritance for gene: ZMPSTE24 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ZMPSTE24 were set to 12913070; 15317753; 20034068; 16297189; 18435794\nPhenotypes for gene: ZMPSTE24 were set to Mandibuloacral dysplasia with type B lipodystrophy, 608612","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2020-01-17T14:20:18.475069+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZFP57 was added\ngene: ZFP57 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: ZFP57 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ZFP57 were set to Diabetes mellitus, transient neonatal, 1, 601410; Transient Neonatal Diabetes; Transient Neonatal Diabetes, Recessive","entity_name":"ZFP57","entity_type":"gene"},{"created":"2020-01-17T14:20:18.392330+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ZBTB20 was added\ngene: ZBTB20 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: ZBTB20 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ZBTB20 were set to 20644156; 25017102\nPhenotypes for gene: ZBTB20 were set to Primrose syndrome (tall stature, macrocephaly, intellectual disability, disturbed behaviour, unusual facial features, diabetes, deafness, progressive muscle wasting and ectopic calcifications); Primrose syndrome, 259050","entity_name":"ZBTB20","entity_type":"gene"},{"created":"2020-01-17T14:20:18.307572+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WFS1 was added\ngene: WFS1 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: WFS1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: WFS1 were set to 27185633; 27217304\nPhenotypes for gene: WFS1 were set to Wolfram-like syndrome, autosomal dominant, 614296; Wolfram syndrome, 222300; Deafness, autosomal dominant 6/14/38, 600965; ?Cataract 41,116400; {Diabetes mellitus, noninsulin-dependent, association with}, 125853; Deafness,autosomal dominant 6/14/38, 600965; {Diabetes mellitus, noninsulin-dependent,association with}; diabetes insipidus or optic atrophy","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-01-17T14:20:18.221730+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRMT10A was added\ngene: TRMT10A was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: TRMT10A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TRMT10A were set to 26297882; 24204302\nPhenotypes for gene: TRMT10A were set to Autosomal recessive juvenile-onset diabetes with microcephaly, epilepsy and intellectual disability; failure to thrive and microcephaly, ketoacidosis at onset of diabetes and islet cell autoantibodies; young onset diabetes, short stature and microcephaly with intellectual disability; Microcephaly, short stature, and impaired glucose metabolism 1, 616033","entity_name":"TRMT10A","entity_type":"gene"},{"created":"2020-01-17T14:20:18.140104+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TFR2 was added\ngene: TFR2 was added to Monogenic diabetes. Sources: Expert Review,Expert Review Green\nMode of inheritance for gene: TFR2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TFR2 were set to Hemochromatosis, type 3 604250","entity_name":"TFR2","entity_type":"gene"},{"created":"2020-01-17T14:20:18.053829+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: STAT3 was added\ngene: STAT3 was added to Monogenic diabetes. Sources: UKGTN,Expert Review Green\nMode of inheritance for gene: STAT3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: STAT3 were set to 25038750; 27167055\nMode of pathogenicity for gene: STAT3 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"STAT3","entity_type":"gene"},{"created":"2020-01-17T14:20:17.969077+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: STAT1 was added\ngene: STAT1 was added to Monogenic diabetes. Sources: Expert Review,Expert Review Red\nMode of inheritance for gene: STAT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: STAT1 were set to 23534974\nMode of pathogenicity for gene: STAT1 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"STAT1","entity_type":"gene"},{"created":"2020-01-17T14:20:17.891800+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC40A1 was added\ngene: SLC40A1 was added to Monogenic diabetes. Sources: Expert Review,Expert Review Green\nMode of inheritance for gene: SLC40A1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SLC40A1 were set to Hemochromatosis, type 4 606069","entity_name":"SLC40A1","entity_type":"gene"},{"created":"2020-01-17T14:20:17.812696+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC2A2 was added\ngene: SLC2A2 was added to Monogenic diabetes. Sources: Radboud University Medical Center, Nijmegen,Expert Review Green,UKGTN\nMode of inheritance for gene: SLC2A2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC2A2 were set to PMID: 23456528; 22831748; 22660720\nPhenotypes for gene: SLC2A2 were set to {Diabetes mellitus, noninsulin-dependent}; Fanconi-Bickel syndrome","entity_name":"SLC2A2","entity_type":"gene"},{"created":"2020-01-17T14:20:17.719712+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC29A3 was added\ngene: SLC29A3 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: SLC29A3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC29A3 were set to 19336477\nPhenotypes for gene: SLC29A3 were set to Histiocytosis-lymphadenopathy plus syndrome,602782; Pigmented hypertrichotic dermatosis with insulin-dependent diabetes (PHID) syndrome; H syndrome (hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and hyperglycaemia) and PHID syndrome (pigmented hypertrichosis with insulin dependent diabetes)","entity_name":"SLC29A3","entity_type":"gene"},{"created":"2020-01-17T14:20:17.635312+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SLC19A2 was added\ngene: SLC19A2 was added to Monogenic diabetes. Sources: UKGTN,Expert Review Green\nMode of inheritance for gene: SLC19A2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC19A2 were set to 26549656; 26839896\nPhenotypes for gene: SLC19A2 were set to Thiamine-responsive megaloblastic anemia syndrome; MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUS AND SENSORINEURAL DEAFNESS ROGERS SYNDROME","entity_name":"SLC19A2","entity_type":"gene"},{"created":"2020-01-17T14:20:17.557091+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RFX6 was added\ngene: RFX6 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: RFX6 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RFX6 were set to 27167055; 27185633; 26770845; 26761945; 26264437; 26559129; 25048417\nPhenotypes for gene: RFX6 were set to Mitchell-Riley syndrome, 615710; Neonatal diabetes, intestinal atresia and hepatobiliary abnormalities; recessive syndromic diabetes and autosomal dominant MODY","entity_name":"RFX6","entity_type":"gene"},{"created":"2020-01-17T14:20:17.476379+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PTF1A was added\ngene: PTF1A was added to Monogenic diabetes. Sources: Radboud University Medical Center, Nijmegen,Expert Review Green,UKGTN\nMode of inheritance for gene: PTF1A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PTF1A were set to Permanent neonatal diabetes mellitus (PNDM); Diabetes mellitus, permanent neonatal, with cerebellar agenesis, 609069","entity_name":"PTF1A","entity_type":"gene"},{"created":"2020-01-17T14:20:17.384684+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PPP1R15B was added\ngene: PPP1R15B was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: PPP1R15B was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PPP1R15B were set to Autosomal recessive juvenile-onset diabetes with microcephaly, epilepsy and intellectual disability,616817","entity_name":"PPP1R15B","entity_type":"gene"},{"created":"2020-01-17T14:20:17.301130+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PPARG was added\ngene: PPARG was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: PPARG was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: PPARG were set to Insulin resistance, severe, digenic; FPLD3; Obesity, severe, 601665; {Diabetes, type 2}, 125853; Lipodystrophy, familial partial, type 3; Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension; Insulin resistance, severe, digenic 604367; [Obesity, resistance to]; Lipodystrophy, familial partial, type 3, 604367; Insulin resistance, severe, digenic, 604367; Lipodystrophy, familial partial, type 3 604367; LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; Carotid intimal medial thickness 1, 609338","entity_name":"PPARG","entity_type":"gene"},{"created":"2020-01-17T14:20:17.220497+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: POLD1 was added\ngene: POLD1 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: POLD1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: POLD1 were set to 23770608\nPhenotypes for gene: POLD1 were set to Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome; Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, 615381; multisystem disorder that includes subcutaneous lipodystrophy, deafness, mandibular hypoplasia and hypogonadism in males\nMode of pathogenicity for gene: POLD1 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"POLD1","entity_type":"gene"},{"created":"2020-01-17T14:20:17.135495+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PLIN1 was added\ngene: PLIN1 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: PLIN1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PLIN1 were set to 11371650; 21345103; 25695774; 30020498\nPhenotypes for gene: PLIN1 were set to Lipodystrophy, familial partial, type 4, 613877; partial lipodystrophy, severe dyslipidemia, and insulin-resistant diabetes; Severe insulin resistance, partial lipodystrophy and diabetes","entity_name":"PLIN1","entity_type":"gene"},{"created":"2020-01-17T14:20:17.050073+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PIK3R1 was added\ngene: PIK3R1 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: PIK3R1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PIK3R1 were set to 23810378\nPhenotypes for gene: PIK3R1 were set to Short stature, hyperextensibility of joints and/or inguinal hernia, ocular depression, Rieger anomaly, and teething delay (SHORT) syndrome, 269880; SHORT syndrome\nMode of pathogenicity for gene: PIK3R1 was set to Other - please provide details in the comments","entity_name":"PIK3R1","entity_type":"gene"},{"created":"2020-01-17T14:20:16.970537+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PDX1 was added\ngene: PDX1 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: PDX1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PDX1 were set to Permanent neonatal diabetes; Maturity-Onset Diabetes Of The Young; Maturity-onset diabetes of the young (MODY); MODY type IV; Recessive neonatal diabetes, pancreatic agenesis and dominant MODY, 606392; MODY4; Pancreatic agenesis 1; MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 4","entity_name":"PDX1","entity_type":"gene"},{"created":"2020-01-17T14:20:16.888965+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PCBD1 was added\ngene: PCBD1 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: PCBD1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PCBD1 were set to 24204001; 24848070\nPhenotypes for gene: PCBD1 were set to Hyperphenylalaninemia, BH4-deficient, D, 264070; Recessive neonatal hyperphenylalaninemia and later onset diabetes (puberty)","entity_name":"PCBD1","entity_type":"gene"},{"created":"2020-01-17T14:20:16.808949+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PAX6 was added\ngene: PAX6 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: PAX6 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: PAX6 were set to Aniridia 106210; diabetes","entity_name":"PAX6","entity_type":"gene"},{"created":"2020-01-17T14:20:16.730318+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PAX4 was added\ngene: PAX4 was added to Monogenic diabetes. Sources: Expert Review Red,Radboud University Medical Center, Nijmegen\nMode of inheritance for gene: PAX4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: PAX4 were set to Maturity-onset diabetes of the young, type IX, 612225; Maturity Onset Diabetes of the Young","entity_name":"PAX4","entity_type":"gene"},{"created":"2020-01-17T14:20:16.651271+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NKX2-2 was added\ngene: NKX2-2 was added to Monogenic diabetes. Sources: UKGTN,Expert Review Green\nMode of inheritance for gene: NKX2-2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NKX2-2 were set to 24411943","entity_name":"NKX2-2","entity_type":"gene"},{"created":"2020-01-17T14:20:16.576303+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NEUROG3 was added\ngene: NEUROG3 was added to Monogenic diabetes. Sources: UKGTN,Expert Review Green\nMode of inheritance for gene: NEUROG3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NEUROG3 were set to 25650326; 26288179","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2020-01-17T14:20:16.499642+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NEUROD1 was added\ngene: NEUROD1 was added to Monogenic diabetes. Sources: Expert Review Green,NHS GMS\nMode of inheritance for gene: NEUROD1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: NEUROD1 were set to 20573748; 10545951; 26773576; 26669242\nPhenotypes for gene: NEUROD1 were set to MODY6; Maturity-Onset Diabetes Of The Young; MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6; {Diabetes mellitus, noninsulin-dependent}, 125853; Maturity Onset Diabetes of the Young; Maturity-onset diabetes of the young 6, 606394; Permanent neonatal diabetes and cerebellar agenesis","entity_name":"NEUROD1","entity_type":"gene"},{"created":"2020-01-17T14:20:16.422820+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MNX1 was added\ngene: MNX1 was added to Monogenic diabetes. Sources: UKGTN,Expert Review Green\nMode of inheritance for gene: MNX1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MNX1 were set to 24411943; 23562494; 26534984","entity_name":"MNX1","entity_type":"gene"},{"created":"2020-01-17T14:20:16.341404+11:00","panel_name":"Monogenic diabetes","panel_id":3093,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LRBA was added\ngene: LRBA was added to Monogenic diabetes. Sources: Expert Review,Expert Review Green\nMode of inheritance for gene: LRBA was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: LRBA were set to 25468195; 25479458; 26206937; 26745254; 27057999\nPhenotypes for gene: LRBA were set to Immunodeficiency, common variable, 8, with autoimmunity","entity_name":"LRBA","entity_type":"gene"}]}