{"count":220828,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1003","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1001","results":[{"created":"2022-02-08T20:56:01.911132+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3200","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FRMPD4 as ready","entity_name":"FRMPD4","entity_type":"gene"},{"created":"2022-02-08T20:56:01.899217+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3200","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: frmpd4 has been classified as Green List (High Evidence).","entity_name":"FRMPD4","entity_type":"gene"},{"created":"2022-02-08T20:55:57.356120+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3200","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FRMPD4 were changed from Intellectual Disability to Intellectual Disability, X-linked 104, MIM#300983","entity_name":"FRMPD4","entity_type":"gene"},{"created":"2022-02-08T20:55:37.664451+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3199","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FRMPD4 were set to ","entity_name":"FRMPD4","entity_type":"gene"},{"created":"2022-02-08T20:55:25.507852+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3198","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FRMPD4 as Green List (high evidence)","entity_name":"FRMPD4","entity_type":"gene"},{"created":"2022-02-08T20:55:25.496091+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3198","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: frmpd4 has been classified as Green List (High Evidence).","entity_name":"FRMPD4","entity_type":"gene"},{"created":"2022-02-08T20:55:12.751685+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3197","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Multiple affected individuals from unrelated families.; to: Multiple affected individuals from unrelated families. Corpus callosum abnormalities, retrognathia reported.","entity_name":"FRMPD4","entity_type":"gene"},{"created":"2022-02-08T20:53:57.766525+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3197","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXP4 as ready","entity_name":"FOXP4","entity_type":"gene"},{"created":"2022-02-08T20:53:57.747467+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3197","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxp4 has been classified as Amber List (Moderate Evidence).","entity_name":"FOXP4","entity_type":"gene"},{"created":"2022-02-08T20:53:36.198384+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3197","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FOXP4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FOXP4","entity_type":"gene"},{"created":"2022-02-08T20:52:35.618229+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3196","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXP2 as ready","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:52:35.606300+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3196","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxp2 has been classified as Red List (Low Evidence).","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:52:14.328935+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3196","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXP2 were changed from SPEECH-LANGUAGE DISORDER 1 to Speech-language disorder-1, MIM# 602081","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:52:00.448887+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3195","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXP2 were set to ","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:51:45.580458+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3194","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FOXP2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:51:35.411671+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3193","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FOXP2 as Red List (low evidence)","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:51:35.401151+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3193","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxp2 has been classified as Red List (Low Evidence).","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:51:23.144560+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3192","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association but typically presents post-natally.","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:51:10.753825+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3192","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FOXP2: Changed rating: RED","entity_name":"FOXP2","entity_type":"gene"},{"created":"2022-02-08T20:50:00.737948+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3192","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FIG4 as ready","entity_name":"FIG4","entity_type":"gene"},{"created":"2022-02-08T20:50:00.726708+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3192","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fig4 has been classified as Green List (High Evidence).","entity_name":"FIG4","entity_type":"gene"},{"created":"2022-02-08T20:49:52.567161+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3192","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FIG4 were changed from Charcot-Marie-Tooth disease, type 4J, OMIM:611228; Charcot-Marie-Tooth disease type 4J, MONDO:0012640; Yunis-Varon syndrome, OMIM:216340; Yunis-Varon syndrome, MONDO:0008995; ?Polymicrogyria, bilateral temporooccipital, OMIM:612691; Bilateral parasagittal parieto-occipital polymicrogyria, MONDO:0012986 to Yunis-Varon syndrome, OMIM:216340; Yunis-Varon syndrome, MONDO:0008995; ?Polymicrogyria, bilateral temporooccipital, OMIM:612691; Bilateral parasagittal parieto-occipital polymicrogyria, MONDO:0012986","entity_name":"FIG4","entity_type":"gene"},{"created":"2022-02-08T20:49:23.849556+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3191","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FIG4 were set to ","entity_name":"FIG4","entity_type":"gene"},{"created":"2022-02-08T20:49:05.418905+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3190","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FIG4 as Green List (high evidence)","entity_name":"FIG4","entity_type":"gene"},{"created":"2022-02-08T20:49:05.406708+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3190","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fig4 has been classified as Green List (High Evidence).","entity_name":"FIG4","entity_type":"gene"},{"created":"2022-02-08T20:48:30.526379+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3189","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCM as ready","entity_name":"FANCM","entity_type":"gene"},{"created":"2022-02-08T20:48:30.513091+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3189","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancm has been classified as Red List (Low Evidence).","entity_name":"FANCM","entity_type":"gene"},{"created":"2022-02-08T20:48:26.619572+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3189","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCM were changed from FANCONI ANEMIA; FANCM-RELATED FANCONI ANEMIA to Fanconi anaemia","entity_name":"FANCM","entity_type":"gene"},{"created":"2022-02-08T20:48:06.921347+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3188","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FANCM as Red List (low evidence)","entity_name":"FANCM","entity_type":"gene"},{"created":"2022-02-08T20:48:06.910152+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3188","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancm has been classified as Red List (Low Evidence).","entity_name":"FANCM","entity_type":"gene"},{"created":"2022-02-08T20:47:41.668044+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3187","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCL as ready","entity_name":"FANCL","entity_type":"gene"},{"created":"2022-02-08T20:47:41.656868+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3187","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancl has been classified as Green List (High Evidence).","entity_name":"FANCL","entity_type":"gene"},{"created":"2022-02-08T20:47:37.100507+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3187","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCL were set to ","entity_name":"FANCL","entity_type":"gene"},{"created":"2022-02-08T20:47:24.503420+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3186","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FANCL as Green List (high evidence)","entity_name":"FANCL","entity_type":"gene"},{"created":"2022-02-08T20:47:24.492530+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3186","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancl has been classified as Green List (High Evidence).","entity_name":"FANCL","entity_type":"gene"},{"created":"2022-02-08T20:45:30.872717+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.36","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: THUMPD1 as ready","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:45:30.862935+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.36","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:45:24.975445+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.36","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: THUMPD1 were changed from Syndromic form of intellectual disability associated with developmental delay, behavioral abnormalities, hearing loss and facial dysmorphism, AR to Syndromic disease, MONDO:0002254, THUMPD1-related","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:44:59.992058+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.35","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: THUMPD1 as Green List (high evidence)","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:44:59.981449+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:44:45.525131+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4497","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: THUMPD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:44:36.380527+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4497","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: THUMPD1 as ready","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:44:36.370761+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4497","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:44:32.167119+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4497","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: THUMPD1 were changed from Syndromic form of intellectual disability associated with developmental delay, behavioral abnormalities, hearing loss and facial dysmorphism, AR to Syndromic disease, MONDO:0002254, THUMPD1-related","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:44:00.682868+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4496","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: THUMPD1 as Green List (high evidence)","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:44:00.671584+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4496","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:43:20.700904+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.116","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: THUMPD1 as ready","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:43:20.691391+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.116","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:43:18.580885+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.116","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: THUMPD1 were changed from Syndromic form of intellectual disability associated with developmental delay, behavioral abnormalities, hearing loss and facial dysmorphism, AR to Syndromic disease, MONDO:0002254, THUMPD1-related","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:42:50.507421+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.115","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: THUMPD1 as Green List (high evidence)","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:42:50.495052+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.115","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:42:15.538330+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.104","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: THUMPD1 as ready","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:42:15.522522+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.104","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:42:12.995308+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.104","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: THUMPD1 were changed from Syndromic form of intellectual disability associated with developmental delay, behavioral abnormalities, hearing loss and facial dysmorphism, AR to Syndromic disease, MONDO:0002254, THUMPD1-related","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:41:43.822084+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.103","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: THUMPD1 as Green List (high evidence)","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:41:43.813063+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.103","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:39:13.954037+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10940","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: THUMPD1 as ready","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:39:13.938771+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10940","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:35:39.967116+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10940","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: THUMPD1 were changed from Syndromic form of intellectual disability associated with developmental delay, behavioral abnormalities, hearing loss and facial dysmorphism, AR to Syndromic disease, MONDO:0002254, THUMPD1-related","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:35:16.004886+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10939","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: THUMPD1 as Green List (high evidence)","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:35:15.993577+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10939","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thumpd1 has been classified as Green List (High Evidence).","entity_name":"THUMPD1","entity_type":"gene"},{"created":"2022-02-08T20:33:32.153585+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3185","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SF3B2 as ready","entity_name":"SF3B2","entity_type":"gene"},{"created":"2022-02-08T20:33:32.144514+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3185","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sf3b2 has been classified as Green List (High Evidence).","entity_name":"SF3B2","entity_type":"gene"},{"created":"2022-02-08T20:33:25.726896+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3185","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SF3B2 as Green List (high evidence)","entity_name":"SF3B2","entity_type":"gene"},{"created":"2022-02-08T20:33:25.715543+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3185","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sf3b2 has been classified as Green List (High Evidence).","entity_name":"SF3B2","entity_type":"gene"},{"created":"2022-02-08T20:32:57.263031+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTEN as ready","entity_name":"PTEN","entity_type":"gene"},{"created":"2022-02-08T20:32:57.252463+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pten has been classified as Red List (Low Evidence).","entity_name":"PTEN","entity_type":"gene"},{"created":"2022-02-08T20:32:53.730109+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PTEN were changed from  to Colitis","entity_name":"PTEN","entity_type":"gene"},{"created":"2022-02-08T20:32:04.808833+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PTEN were set to ","entity_name":"PTEN","entity_type":"gene"},{"created":"2022-02-08T20:31:35.730914+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PTEN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PTEN","entity_type":"gene"},{"created":"2022-02-08T20:31:03.733055+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PTEN as Red List (low evidence)","entity_name":"PTEN","entity_type":"gene"},{"created":"2022-02-08T20:31:03.723569+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pten has been classified as Red List (Low Evidence).","entity_name":"PTEN","entity_type":"gene"},{"created":"2022-02-08T20:29:55.718496+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3184","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SEPT9 as ready","entity_name":"SEPT9","entity_type":"gene"},{"created":"2022-02-08T20:29:55.708910+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3184","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sept9 has been classified as Red List (Low Evidence).","entity_name":"SEPT9","entity_type":"gene"},{"created":"2022-02-08T20:29:44.545795+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3184","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SEPT9 as Red List (low evidence)","entity_name":"SEPT9","entity_type":"gene"},{"created":"2022-02-08T20:29:44.528229+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3184","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sept9 has been classified as Red List (Low Evidence).","entity_name":"SEPT9","entity_type":"gene"},{"created":"2022-02-08T20:29:29.635059+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3183","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SEPT9: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SEPT9","entity_type":"gene"},{"created":"2022-02-08T20:28:50.257748+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3183","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLCH1 as ready","entity_name":"PLCH1","entity_type":"gene"},{"created":"2022-02-08T20:28:50.245431+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3183","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plch1 has been classified as Amber List (Moderate Evidence).","entity_name":"PLCH1","entity_type":"gene"},{"created":"2022-02-08T20:28:44.079847+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3183","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PLCH1 as Amber List (moderate evidence)","entity_name":"PLCH1","entity_type":"gene"},{"created":"2022-02-08T20:28:44.062958+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3183","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plch1 has been classified as Amber List (Moderate Evidence).","entity_name":"PLCH1","entity_type":"gene"},{"created":"2022-02-08T20:27:55.300401+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3182","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLEKHA5 as ready","entity_name":"PLEKHA5","entity_type":"gene"},{"created":"2022-02-08T20:27:55.291188+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3182","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plekha5 has been classified as Amber List (Moderate Evidence).","entity_name":"PLEKHA5","entity_type":"gene"},{"created":"2022-02-08T20:27:46.382709+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3182","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PLEKHA5 as Amber List (moderate evidence)","entity_name":"PLEKHA5","entity_type":"gene"},{"created":"2022-02-08T20:27:46.367992+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3182","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plekha5 has been classified as Amber List (Moderate Evidence).","entity_name":"PLEKHA5","entity_type":"gene"},{"created":"2022-02-08T20:27:18.976636+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3181","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLEKHA7 as ready","entity_name":"PLEKHA7","entity_type":"gene"},{"created":"2022-02-08T20:27:18.964712+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plekha7 has been classified as Amber List (Moderate Evidence).","entity_name":"PLEKHA7","entity_type":"gene"},{"created":"2022-02-08T20:27:09.606694+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3181","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PLEKHA7 as Amber List (moderate evidence)","entity_name":"PLEKHA7","entity_type":"gene"},{"created":"2022-02-08T20:27:09.593772+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3181","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plekha7 has been classified as Amber List (Moderate Evidence).","entity_name":"PLEKHA7","entity_type":"gene"},{"created":"2022-02-08T20:26:26.268430+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3180","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PPP1R13L as ready","entity_name":"PPP1R13L","entity_type":"gene"},{"created":"2022-02-08T20:26:26.256906+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3180","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1r13l has been classified as Green List (High Evidence).","entity_name":"PPP1R13L","entity_type":"gene"},{"created":"2022-02-08T20:26:14.779798+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3180","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PPP1R13L as Green List (high evidence)","entity_name":"PPP1R13L","entity_type":"gene"},{"created":"2022-02-08T20:26:14.767621+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3180","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1r13l has been classified as Green List (High Evidence).","entity_name":"PPP1R13L","entity_type":"gene"},{"created":"2022-02-08T20:25:37.083638+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3179","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: METTL23 as ready","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-02-08T20:25:37.073819+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3179","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mettl23 has been classified as Red List (Low Evidence).","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-02-08T20:25:31.261582+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3179","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: METTL23 as Red List (low evidence)","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-02-08T20:25:31.250260+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3179","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mettl23 has been classified as Red List (Low Evidence).","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-02-08T20:24:32.655831+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3178","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRRC32 as ready","entity_name":"LRRC32","entity_type":"gene"},{"created":"2022-02-08T20:24:32.644281+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3178","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrrc32 has been classified as Amber List (Moderate Evidence).","entity_name":"LRRC32","entity_type":"gene"},{"created":"2022-02-08T20:24:24.981195+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3178","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LRRC32 as Amber List (moderate evidence)","entity_name":"LRRC32","entity_type":"gene"}]}