{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1340","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1338","results":[{"created":"2021-04-24T18:53:52.961557+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7335","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGIF1 as ready","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:53:52.948314+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7335","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgif1 has been classified as Green List (High Evidence).","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:53:44.783319+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7335","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGIF1 were changed from  to Holoprosencephaly 4, MIM# 142946; MONDO:0007734","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:53:16.357652+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7334","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGIF1 were set to ","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:52:42.267908+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7333","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGIF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:52:22.761039+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7332","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGIF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10835638, 16323008; Phenotypes: Holoprosencephaly 4, MIM# 142946, MONDO:0007734; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:51:22.183457+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGIF1 as ready","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:51:22.171796+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgif1 has been classified as Green List (High Evidence).","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:51:19.059057+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGIF1 were changed from  to Holoprosencephaly 4, MIM# 142946; MONDO:0007734","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:50:50.649997+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGIF1 were set to ","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:50:27.521969+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGIF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:49:55.566102+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGIF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10835638, 16323008; Phenotypes: Holoprosencephaly 4, MIM# 142946, MONDO:0007734; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-04-24T18:23:46.040264+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7332","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SIX3 as ready","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:23:46.030103+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7332","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: six3 has been classified as Green List (High Evidence).","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:23:39.053744+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7332","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SIX3 were changed from  to Holoprosencephaly 2, MIM# 157170; MONDO:0007999","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:23:20.005170+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7331","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SIX3 were set to ","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:23:04.456392+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7330","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SIX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:22:46.335365+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7329","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SIX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 10369266, 16323008, 19346217; Phenotypes: Holoprosencephaly 2, MIM# 157170, MONDO:0007999; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:22:19.518555+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SIX3 as ready","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:22:19.507508+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: six3 has been classified as Green List (High Evidence).","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:22:12.384502+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SIX3 were changed from  to Holoprosencephaly 2, MIM# 157170; MONDO:0007999","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:21:40.863599+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SIX3 were set to ","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:21:13.490247+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SIX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:20:23.758537+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SIX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 10369266, 16323008, 19346217; Phenotypes: Holoprosencephaly 2, MIM# 157170, MONDO:0007999; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SIX3","entity_type":"gene"},{"created":"2021-04-24T18:16:17.892128+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTCH1 as ready","entity_name":"PTCH1","entity_type":"gene"},{"created":"2021-04-24T18:16:17.880261+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ptch1 has been classified as Green List (High Evidence).","entity_name":"PTCH1","entity_type":"gene"},{"created":"2021-04-24T18:16:14.621786+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PTCH1 were changed from  to Holoprosencephaly 7, MIM# 610828","entity_name":"PTCH1","entity_type":"gene"},{"created":"2021-04-24T18:15:47.137189+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PTCH1 were set to ","entity_name":"PTCH1","entity_type":"gene"},{"created":"2021-04-24T18:15:18.589306+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PTCH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PTCH1","entity_type":"gene"},{"created":"2021-04-24T18:14:45.759082+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PTCH1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11941477, 17001668, 29575684; Phenotypes: Holoprosencephaly 7, MIM# 610828; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PTCH1","entity_type":"gene"},{"created":"2021-04-24T18:11:50.216632+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLI2 as ready","entity_name":"GLI2","entity_type":"gene"},{"created":"2021-04-24T18:11:50.207180+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gli2 has been classified as Green List (High Evidence).","entity_name":"GLI2","entity_type":"gene"},{"created":"2021-04-24T18:11:46.778977+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GLI2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GLI2","entity_type":"gene"},{"created":"2021-04-24T18:11:29.380657+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLI2 were set to ","entity_name":"GLI2","entity_type":"gene"},{"created":"2021-04-24T18:10:57.132758+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GLI2 were changed from  to Holoprosencephaly 9, MIM# 610829; MONDO:0012563","entity_name":"GLI2","entity_type":"gene"},{"created":"2021-04-24T18:10:09.102992+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GLI2: Rating: GREEN; Mode of pathogenicity: None; Publications: 14581620, 17096318, 33235745, 27585885; Phenotypes: Holoprosencephaly 9, MIM# 610829; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GLI2","entity_type":"gene"},{"created":"2021-04-24T18:07:09.640466+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR1 as ready","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-04-24T18:07:09.631529+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr1 has been classified as Green List (High Evidence).","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-04-24T18:07:06.263374+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGFR1 were changed from  to Hartsfield syndrome, MIM# 615465","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-04-24T18:06:38.259805+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGFR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-04-24T18:06:14.425546+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FGFR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hartsfield syndrome, MIM# 615465; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-04-24T18:05:11.673084+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGF8 as ready","entity_name":"FGF8","entity_type":"gene"},{"created":"2021-04-24T18:05:11.661493+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf8 has been classified as Green List (High Evidence).","entity_name":"FGF8","entity_type":"gene"},{"created":"2021-04-24T18:05:09.058187+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGF8 were changed from  to Holoprosencephaly; MONDO:0016296","entity_name":"FGF8","entity_type":"gene"},{"created":"2021-04-24T18:04:46.334795+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FGF8 were set to ","entity_name":"FGF8","entity_type":"gene"},{"created":"2021-04-24T18:04:08.931770+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGF8 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGF8","entity_type":"gene"},{"created":"2021-04-24T18:03:39.188998+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FGF8: Changed phenotypes: Holoprosencephaly, MONDO:0016296","entity_name":"FGF8","entity_type":"gene"},{"created":"2021-04-24T18:02:40.739168+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FGF8: Rating: GREEN; Mode of pathogenicity: None; Publications: 27363716, 29584859; Phenotypes: Holoprosencephaly; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGF8","entity_type":"gene"},{"created":"2021-04-24T17:59:51.788024+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DISP1 as ready","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:59:51.770439+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: disp1 has been classified as Amber List (Moderate Evidence).","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:59:46.408236+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7329","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DISP1 as ready","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:59:46.399264+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7329","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: disp1 has been classified as Amber List (Moderate Evidence).","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:59:38.663159+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7329","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DISP1 were changed from  to Holoprosencephaly","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:59:20.319183+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7328","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DISP1 were set to ","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:59:01.852171+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7327","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DISP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:58:45.363648+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7326","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DISP1 as Amber List (moderate evidence)","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:58:45.352909+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7326","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: disp1 has been classified as Amber List (Moderate Evidence).","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:58:28.142614+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7325","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DISP1: Rating: AMBER; Mode of pathogenicity: None; Publications: 19184110, 26748417, 23542665; Phenotypes: Holoprosencephaly; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:58:27.041298+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DISP1 were changed from  to Holoprosencephaly","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:57:58.153707+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DISP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:57:24.188755+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: DISP1 was changed from  to Other","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:56:34.833865+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DISP1 were set to ","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:56:08.736713+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DISP1 as Amber List (moderate evidence)","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:56:08.726178+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: disp1 has been classified as Amber List (Moderate Evidence).","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T17:55:35.375834+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DISP1: Rating: AMBER; Mode of pathogenicity: Other; Publications: 19184110, 26748417, 23542665; Phenotypes: Holoprosencephaly; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DISP1","entity_type":"gene"},{"created":"2021-04-24T15:03:10.202514+10:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"1.5","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CDON were changed from Holoprosencephaly 11\tMIM#614226 to Coloboma","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T15:01:44.539477+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDON as ready","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T15:01:44.528020+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdon has been classified as Green List (High Evidence).","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T15:01:41.845812+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CDON were changed from  to Holoprosencephaly 11, MIM# 614226; MONDO:0013642","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T15:01:19.186769+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CDON were set to ","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T15:00:49.268492+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CDON was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T15:00:22.672937+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: CDON: Changed phenotypes: Holoprosencephaly 11, MIM# 614226, MONDO:0013642","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T15:00:02.660604+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: >5 unrelated families reported, however note some of the variants are present at a very low frequenting in gnomad (1-4) and some are inherited. Mouse model.; to: >5 unrelated families reported, however note some of the variants are present at a very low frequentcy in gnomad (1-4) and some are inherited. Mouse model.","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T14:59:52.554330+10:00","panel_name":"Holoprosencephaly and septo-optic dysplasia","panel_id":112,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CDON: Rating: GREEN; Mode of pathogenicity: None; Publications: 21802063, 26529631, 26728615, 23071453; Phenotypes: Holoprosencephaly 11, MIM# 614226; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CDON","entity_type":"gene"},{"created":"2021-04-24T14:48:52.787534+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"1.0","user_name":"Zornitza Stark","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2021-04-24T14:48:23.923427+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR2 as ready","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-04-24T14:48:23.913098+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr2 has been classified as Green List (High Evidence).","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-04-24T14:48:20.404133+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGFR2 as Green List (high evidence)","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-04-24T14:48:20.394252+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr2 has been classified as Green List (High Evidence).","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-04-24T14:46:31.793859+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBX3 as ready","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:46:31.783467+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx3 has been classified as Green List (High Evidence).","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:46:24.325643+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBX3 were changed from  to Ulnar-mammary syndrome, MIM# 181450; MONDO:0008411","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:46:00.760336+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBX3 were set to ","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:45:31.430229+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:44:56.588486+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7325","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBX3 as ready","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:44:56.578605+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7325","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx3 has been classified as Green List (High Evidence).","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:44:48.027708+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7325","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBX3 were changed from  to Ulnar-mammary syndrome, MIM# 181450; MONDO:0008411","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:44:28.987698+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7324","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBX3 were set to ","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:44:10.586132+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7323","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:43:53.225230+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7322","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 9207801, 19938096, 28145909; Phenotypes: Ulnar-mammary syndrome, MIM# 181450, MONDO:0008411; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:43:05.400685+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 9207801, 19938096, 28145909; Phenotypes: Ulnar-mammary syndrome, MIM# 181450, MONDO:0008411; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-04-24T14:40:13.820770+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLX4 as ready","entity_name":"SLX4","entity_type":"gene"},{"created":"2021-04-24T14:40:13.810218+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slx4 has been classified as Green List (High Evidence).","entity_name":"SLX4","entity_type":"gene"},{"created":"2021-04-24T14:40:10.564191+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLX4 were changed from  to Fanconi anaemia, complementation group P, MIM# 613951; MONDO:0013499","entity_name":"SLX4","entity_type":"gene"},{"created":"2021-04-24T14:39:46.488900+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLX4 were set to ","entity_name":"SLX4","entity_type":"gene"},{"created":"2021-04-24T14:39:17.507288+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLX4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLX4","entity_type":"gene"},{"created":"2021-04-24T14:38:46.406803+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SLX4: Changed phenotypes: Fanconi anaemia, complementation group P, MIM# 613951, MONDO:0013499","entity_name":"SLX4","entity_type":"gene"},{"created":"2021-04-24T14:38:26.895574+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SLX4: Changed phenotypes: Fanconi anaemia, complementation group P, MIM# 613951","entity_name":"SLX4","entity_type":"gene"},{"created":"2021-04-24T14:37:55.713415+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SALL4 as ready","entity_name":"SALL4","entity_type":"gene"},{"created":"2021-04-24T14:37:55.703470+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sall4 has been classified as Green List (High Evidence).","entity_name":"SALL4","entity_type":"gene"}]}