{"count":220313,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=864","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=862","results":[{"created":"2022-05-03T16:27:37.116164+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13602","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HESX1 as ready","entity_name":"HESX1","entity_type":"gene"},{"created":"2022-05-03T16:27:37.096162+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13602","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hesx1 has been classified as Green List (High Evidence).","entity_name":"HESX1","entity_type":"gene"},{"created":"2022-05-03T16:27:28.052984+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13602","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HESX1 were changed from  to Growth hormone deficiency with pituitary anomalies, MIM#182230; Pituitary hormone deficiency, combined, 5, MIM#182230; Septooptic dysplasia, MIM#182230","entity_name":"HESX1","entity_type":"gene"},{"created":"2022-05-03T16:26:46.353510+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13601","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HESX1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"HESX1","entity_type":"gene"},{"created":"2022-05-03T16:26:23.247650+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13600","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HESX1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Growth hormone deficiency with pituitary anomalies, MIM#182230, Pituitary hormone deficiency, combined, 5, MIM#182230, Septooptic dysplasia, MIM#182230; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"HESX1","entity_type":"gene"},{"created":"2022-05-03T09:45:48.662775+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4721","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHD8 were changed from {Autism, susceptibility to, 18} 615032; CHD8-related neurodevelopmental syndrome to {Autism, susceptibility to, 18} 615032; Neurodevelopmental disorder, MONDO:0700092, CHD8-associated","entity_name":"CHD8","entity_type":"gene"},{"created":"2022-05-03T09:44:32.361157+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4720","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: CHD8: Changed phenotypes: {Autism, susceptibility to, 18} 615032, Neurodevelopmental disorder, MONDO:0700092, CHD8-associated","entity_name":"CHD8","entity_type":"gene"},{"created":"2022-05-03T09:43:51.435487+10:00","panel_name":"Overgrowth","panel_id":151,"panel_version":"1.8","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHD8 were changed from {Autism, susceptibility to, 18} 615032; CHD8-related neurodevelopmental syndrome to {Autism, susceptibility to, 18} 615032; Neurodevelopmental disorder, MONDO:0700092, CHD8-associated","entity_name":"CHD8","entity_type":"gene"},{"created":"2022-05-03T09:43:14.932365+10:00","panel_name":"Overgrowth","panel_id":151,"panel_version":"1.7","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: CHD8: Changed phenotypes: {Autism, susceptibility to, 18} 615032, Neurodevelopmental disorder, MONDO:0700092, CHD8-associated","entity_name":"CHD8","entity_type":"gene"},{"created":"2022-05-03T09:42:44.975326+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13600","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHD8 were changed from {Autism, susceptibility to, 18} 615032; CHD8-related neurodevelopmental syndrome to {Autism, susceptibility to, 18} 615032; Neurodevelopmental disorder, MONDO:0700092, CHD8-associated","entity_name":"CHD8","entity_type":"gene"},{"created":"2022-05-03T09:42:04.907210+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13599","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: CHD8: Changed phenotypes: {Autism, susceptibility to, 18} 615032, Neurodevelopmental disorder, MONDO:0700092, CHD8-associated","entity_name":"CHD8","entity_type":"gene"},{"created":"2022-05-03T09:05:42.335096+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13599","user_name":"Samantha Ayres","item_type":"entity","text":"reviewed gene: SLC11A1: Rating: RED; Mode of pathogenicity: None; Publications: 35140349; Phenotypes: {Buruli ulcer, susceptibility to}, MIM#610446, {Mycobacterium tuberculosis, susceptibility to infection by} , MIM#607948; Mode of inheritance: Unknown","entity_name":"SLC11A1","entity_type":"gene"},{"created":"2022-05-02T18:50:38.223886+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4720","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HERC1 as ready","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:50:38.213686+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4720","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: herc1 has been classified as Green List (High Evidence).","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:50:34.004980+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4720","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HERC1 were changed from  to Macrocephaly, dysmorphic facies, and psychomotor retardation, MIM# 617011","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:48:29.992218+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4719","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HERC1 were set to ","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:47:56.219146+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4718","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HERC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:47:21.463355+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4717","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HERC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28323226, 27108999, 26153217, 26138117, 20041218; Phenotypes: Macrocephaly, dysmorphic facies, and psychomotor retardation, MIM# 617011; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:46:32.287077+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13599","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HERC1 as ready","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:46:32.276924+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13599","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: herc1 has been classified as Green List (High Evidence).","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:46:23.145957+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13599","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HERC1 were changed from  to Macrocephaly, dysmorphic facies, and psychomotor retardation, MIM# 617011","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:46:04.111382+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13598","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HERC1 were set to ","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:45:43.833770+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13597","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HERC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:45:22.497056+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13596","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HERC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28323226, 27108999, 26153217, 26138117, 20041218; Phenotypes: Macrocephaly, dysmorphic facies, and psychomotor retardation, MIM# 617011; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-05-02T18:41:41.292396+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13596","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HEPACAM as ready","entity_name":"HEPACAM","entity_type":"gene"},{"created":"2022-05-02T18:41:41.279042+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13596","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hepacam has been classified as Green List (High Evidence).","entity_name":"HEPACAM","entity_type":"gene"},{"created":"2022-05-02T18:41:32.206299+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13596","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HEPACAM were changed from  to Megalencephalic leukoencephalopathy with subcortical cysts 2A, MIM# 613925; Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation, MIM# 613926","entity_name":"HEPACAM","entity_type":"gene"},{"created":"2022-05-02T18:41:11.626422+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13595","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HEPACAM were set to ","entity_name":"HEPACAM","entity_type":"gene"},{"created":"2022-05-02T18:40:49.640202+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13594","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HEPACAM was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"HEPACAM","entity_type":"gene"},{"created":"2022-05-02T18:40:25.311341+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13593","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HEPACAM: Rating: GREEN; Mode of pathogenicity: None; Publications: 21419380, 21419380; Phenotypes: Megalencephalic leukoencephalopathy with subcortical cysts 2A, MIM# 613925, Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation, MIM# 613926; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"HEPACAM","entity_type":"gene"},{"created":"2022-05-02T15:11:18.743033+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13593","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: LIPT2 as ready","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-05-02T15:11:18.729063+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13593","user_name":"Alison Yeung","item_type":"entity","text":"Gene: lipt2 has been classified as Green List (High Evidence).","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-05-02T15:11:09.668732+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13593","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LIPT2 were changed from  to Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, MIM#617668","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-05-02T14:51:36.517500+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13592","user_name":"Samantha Ayres","item_type":"entity","text":"reviewed gene: SIL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24176978, 16282977, 20301371; Phenotypes: Marinesco-Sjogren syndrome, MIM#248800, MONDO#0009567; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SIL1","entity_type":"gene"},{"created":"2022-05-02T14:09:08.158407+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNASE2 were changed from Auto-inflammatory disorder; splenomegaly; glomerulonephritis; liver fibrosis; arthritis; HLH to Autoinflammatory-pancytopaenia syndrome, MIM# 619858","entity_name":"DNASE2","entity_type":"gene"},{"created":"2022-05-02T14:08:31.900459+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DNASE2: Changed phenotypes: Autoinflammatory-pancytopaenia syndrome, MIM# 619858","entity_name":"DNASE2","entity_type":"gene"},{"created":"2022-05-02T14:08:07.316146+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13592","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNASE2 were changed from Auto-inflammatory disorder; splenomegaly; glomerulonephritis; liver fibrosis; arthritis; HLH to Autoinflammatory-pancytopaenia syndrome, MIM# 619858","entity_name":"DNASE2","entity_type":"gene"},{"created":"2022-05-02T14:07:40.247347+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13591","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DNASE2: Changed phenotypes: Autoinflammatory-pancytopenia syndrome, MIM# 619858","entity_name":"DNASE2","entity_type":"gene"},{"created":"2022-05-02T12:44:58.354860+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13591","user_name":"Alison Yeung","item_type":"entity","text":"Publications for gene: LIPT2 were set to ","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-05-02T12:44:37.150116+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13590","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: LIPT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LIPT2","entity_type":"gene"},{"created":"2022-05-02T12:40:43.534579+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13589","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: LIPH as ready","entity_name":"LIPH","entity_type":"gene"},{"created":"2022-05-02T12:40:43.507126+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13589","user_name":"Alison Yeung","item_type":"entity","text":"Gene: liph has been classified as Green List (High Evidence).","entity_name":"LIPH","entity_type":"gene"},{"created":"2022-05-02T12:40:40.675130+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13589","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LIPH were changed from  to Woolly hair, autosomal recessive 2 with or without hypotrichosis, MIM# 604379; Hypotrichosis 7, MIM# 604379","entity_name":"LIPH","entity_type":"gene"},{"created":"2022-05-02T12:39:58.923591+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13588","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: LIPH: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Woolly hair, autosomal recessive 2 with or without hypotrichosis, MIM# 604379, Hypotrichosis 7, MIM# 604379; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LIPH","entity_type":"gene"},{"created":"2022-05-02T12:38:02.672625+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13588","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: LIPH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LIPH","entity_type":"gene"},{"created":"2022-05-02T12:34:14.898881+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13587","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: LIPC as ready","entity_name":"LIPC","entity_type":"gene"},{"created":"2022-05-02T12:34:14.887345+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13587","user_name":"Alison Yeung","item_type":"entity","text":"Gene: lipc has been classified as Green List (High Evidence).","entity_name":"LIPC","entity_type":"gene"},{"created":"2022-05-02T12:33:55.844929+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13587","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LIPC were changed from  to Hepatic lipase deficiency MIM#614025; Hyperlipidemia due to hepatic triglyceride lipase deficiency, MONDO:0013533","entity_name":"LIPC","entity_type":"gene"},{"created":"2022-05-02T12:31:28.634554+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13586","user_name":"Alison Yeung","item_type":"entity","text":"Publications for gene: LIPC were set to ","entity_name":"LIPC","entity_type":"gene"},{"created":"2022-05-02T12:30:36.284496+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13585","user_name":"Alison Yeung","item_type":"entity","text":"Added comment: Comment on mode of inheritance: PMID: 1671786, 12777476, 1883393, 22798447 - 7 cases from 3 unrelated families with hepatic lipase deficiency and biallelic variants.\r\nPMID: 26423094 - null mouse had dyslipidemia on a high cholesterol and fat diet\r\nPMID: 23219720, 22464213 - 2 cases with hyperalphalipoproteinemia and heterozygous variants, with supporting in vitro funcitonal assays","entity_name":"LIPC","entity_type":"gene"},{"created":"2022-05-02T12:30:36.248636+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13585","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: LIPC was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LIPC","entity_type":"gene"},{"created":"2022-05-02T12:25:18.798275+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13584","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: LINS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:24:55.357358+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13583","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: LINS1 as ready","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:24:55.340439+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13583","user_name":"Alison Yeung","item_type":"entity","text":"Gene: lins1 has been classified as Green List (High Evidence).","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:24:47.006888+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13583","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LINS1 were changed from  to Intellectual developmental disorder, autosomal recessive 27, MIM# 614340","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:24:07.479260+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13582","user_name":"Alison Yeung","item_type":"entity","text":"Publications for gene: LINS1 were set to ","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:08:45.546386+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4717","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LINS1 were changed from Intellectual developmental disorder, autosomal recessive 27, MIM# 614340 to Intellectual developmental disorder, autosomal recessive 27, MIM# 614340","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:07:56.550575+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4716","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LINS1 were changed from  to Intellectual developmental disorder, autosomal recessive 27, MIM# 614340","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:07:56.179263+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4715","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: LINS1 as ready","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:07:56.169395+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4715","user_name":"Alison Yeung","item_type":"entity","text":"Gene: lins1 has been classified as Green List (High Evidence).","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:07:16.560269+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4715","user_name":"Alison Yeung","item_type":"entity","text":"Publications for gene: LINS1 were set to ","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:06:23.646121+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4714","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: LINS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T12:05:44.520398+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4713","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: LINS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 32802957, 34450347, 32499722, 31922598; Phenotypes: ntellectual developmental disorder, autosomal recessive 27, MIM# 614340; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LINS1","entity_type":"gene"},{"created":"2022-05-02T11:44:40.232573+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13581","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCRT as ready","entity_name":"HCRT","entity_type":"gene"},{"created":"2022-05-02T11:44:40.217359+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13581","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcrt has been classified as Red List (Low Evidence).","entity_name":"HCRT","entity_type":"gene"},{"created":"2022-05-02T11:44:31.003798+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13581","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HCRT were changed from  to Narcolepsy 1 , MIM# 161400","entity_name":"HCRT","entity_type":"gene"},{"created":"2022-05-02T11:44:10.627480+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13580","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HCRT were set to ","entity_name":"HCRT","entity_type":"gene"},{"created":"2022-05-02T11:43:50.200461+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13579","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HCRT was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HCRT","entity_type":"gene"},{"created":"2022-05-02T11:43:31.605540+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13578","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HCRT as Red List (low evidence)","entity_name":"HCRT","entity_type":"gene"},{"created":"2022-05-02T11:43:31.592508+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13578","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcrt has been classified as Red List (Low Evidence).","entity_name":"HCRT","entity_type":"gene"},{"created":"2022-05-02T11:43:20.922660+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13577","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: LIM2 as ready","entity_name":"LIM2","entity_type":"gene"},{"created":"2022-05-02T11:43:20.909607+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13577","user_name":"Alison Yeung","item_type":"entity","text":"Gene: lim2 has been classified as Green List (High Evidence).","entity_name":"LIM2","entity_type":"gene"},{"created":"2022-05-02T11:43:06.723396+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13577","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HCRT: Rating: RED; Mode of pathogenicity: None; Publications: 10973318, 11148249, 11723284; Phenotypes: Narcolepsy 1 , MIM# 161400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HCRT","entity_type":"gene"},{"created":"2022-05-02T11:42:54.603445+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13577","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: LIM2 were changed from  to Cataract 19, multiple types, MIM# 615277","entity_name":"LIM2","entity_type":"gene"},{"created":"2022-05-02T11:42:43.509331+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13576","user_name":"Alison Yeung","item_type":"entity","text":"Publications for gene: LIM2 were set to ","entity_name":"LIM2","entity_type":"gene"},{"created":"2022-05-02T11:42:34.405859+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13575","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: LIM2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LIM2","entity_type":"gene"},{"created":"2022-05-02T11:38:18.934879+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4713","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCN1 as ready","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:38:18.923303+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4713","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcn1 has been classified as Green List (High Evidence).","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:38:10.981356+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4713","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HCN1 were changed from  to Developmental and epileptic encephalopathy 24, MIM# 615871; Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:37:48.629737+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13574","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: LIM2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27814360, 11917274, 18596884, 33708862, 32202185, 21617753; Phenotypes: Cataract 19, multiple types, MIM# 615277; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LIM2","entity_type":"gene"},{"created":"2022-05-02T11:37:29.936124+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4712","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HCN1 were set to ","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:36:53.702278+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4711","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HCN1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:36:15.619553+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4710","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HCN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24747641, 30351409, 30351409; Phenotypes: Developmental and epileptic encephalopathy 24, MIM# 615871, Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:35:27.685524+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1579","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCN1 as ready","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:35:27.675074+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1579","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcn1 has been classified as Green List (High Evidence).","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:35:24.514280+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1579","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HCN1 were changed from  to Developmental and epileptic encephalopathy 24, MIM# 615871; Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:34:47.593346+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1578","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HCN1 were set to ","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:34:12.077374+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1577","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HCN1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:33:33.384621+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1576","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HCN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24747641, 30351409, 30351409; Phenotypes: Developmental and epileptic encephalopathy 24, MIM# 615871, Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:32:53.457065+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13574","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCN1 as ready","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:32:53.417065+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13574","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hcn1 has been classified as Green List (High Evidence).","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:32:42.617225+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13574","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HCN1 were changed from  to Developmental and epileptic encephalopathy 24, MIM# 615871; Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:32:22.580482+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13573","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HCN1 were set to ","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:31:58.963811+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13572","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HCN1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:31:25.706059+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13571","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HCN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24747641, 30351409, 30351409; Phenotypes: Developmental and epileptic encephalopathy 24, MIM# 615871, Generalized epilepsy with febrile seizures plus, type 10, MIM# 618482; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HCN1","entity_type":"gene"},{"created":"2022-05-02T11:26:56.296707+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13571","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCCS as ready","entity_name":"HCCS","entity_type":"gene"},{"created":"2022-05-02T11:26:56.286158+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13571","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hccs has been classified as Green List (High Evidence).","entity_name":"HCCS","entity_type":"gene"},{"created":"2022-05-02T11:26:47.177326+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13571","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HCCS were changed from  to Linear skin defects with multiple congenital anomalies 1, MIM# 309801","entity_name":"HCCS","entity_type":"gene"},{"created":"2022-05-02T11:26:25.010504+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13570","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HCCS were set to ","entity_name":"HCCS","entity_type":"gene"},{"created":"2022-05-02T11:26:03.511391+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13569","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HCCS was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HCCS","entity_type":"gene"}]}