{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1869","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1867","results":[{"created":"2020-04-12T08:52:56.303088+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2141","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAPBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T21:38:08.058520+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2140","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NXN were changed from  to Robinow syndrome, autosomal recessive 2 618529","entity_name":"NXN","entity_type":"gene"},{"created":"2020-04-11T21:37:53.680091+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2139","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NXN were set to ","entity_name":"NXN","entity_type":"gene"},{"created":"2020-04-11T21:37:39.434938+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2138","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NXN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NXN","entity_type":"gene"},{"created":"2020-04-11T21:37:19.809842+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2137","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NXN: Rating: GREEN; Mode of pathogenicity: None; Publications: 29276006; Phenotypes: Robinow syndrome, autosomal recessive 2 618529; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NXN","entity_type":"gene"},{"created":"2020-04-11T21:05:54.161750+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TERT as ready","entity_name":"TERT","entity_type":"gene"},{"created":"2020-04-11T21:05:54.148539+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tert has been classified as Amber List (Moderate Evidence).","entity_name":"TERT","entity_type":"gene"},{"created":"2020-04-11T21:05:52.399445+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2137","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAPBP were set to ","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T21:05:45.704044+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TERT were changed from  to {Dyskeratosis congenita, autosomal dominant 2}, MIM# 613989; {Dyskeratosis congenita, autosomal recessive 4}, MIM# 613989","entity_name":"TERT","entity_type":"gene"},{"created":"2020-04-11T21:05:20.827797+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TERT was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TERT","entity_type":"gene"},{"created":"2020-04-11T21:04:48.736295+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TERT as Amber List (moderate evidence)","entity_name":"TERT","entity_type":"gene"},{"created":"2020-04-11T21:04:48.723369+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tert has been classified as Amber List (Moderate Evidence).","entity_name":"TERT","entity_type":"gene"},{"created":"2020-04-11T21:04:17.704533+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TERT: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: {Dyskeratosis congenita, autosomal dominant 2}, MIM# 613989, {Dyskeratosis congenita, autosomal recessive 4}, MIM# 613989; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TERT","entity_type":"gene"},{"created":"2020-04-11T21:03:04.824500+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TERC as ready","entity_name":"TERC","entity_type":"gene"},{"created":"2020-04-11T21:03:04.811023+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: terc has been classified as Amber List (Moderate Evidence).","entity_name":"TERC","entity_type":"gene"},{"created":"2020-04-11T21:02:28.611102+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TERC were changed from  to Dyskeratosis congenita, autosomal dominant 1, MIM# 127550","entity_name":"TERC","entity_type":"gene"},{"created":"2020-04-11T21:02:00.589228+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TERC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TERC","entity_type":"gene"},{"created":"2020-04-11T21:01:36.879651+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TERC as Amber List (moderate evidence)","entity_name":"TERC","entity_type":"gene"},{"created":"2020-04-11T21:01:36.871160+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: terc has been classified as Amber List (Moderate Evidence).","entity_name":"TERC","entity_type":"gene"},{"created":"2020-04-11T21:01:05.892123+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TERC: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Dyskeratosis congenita, autosomal dominant 1, MIM# 127550; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TERC","entity_type":"gene"},{"created":"2020-04-11T21:00:15.470540+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2136","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAPBP as Red List (low evidence)","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T21:00:15.455284+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2136","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tapbp has been classified as Red List (Low Evidence).","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T21:00:06.102857+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2136","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAPBP as Red List (low evidence)","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T21:00:06.092524+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2136","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tapbp has been classified as Red List (Low Evidence).","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:58:23.316711+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2135","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAPBP: Rating: RED; Mode of pathogenicity: None; Publications: 12149238; Phenotypes: Bare lymphocyte syndrome, type I, MIM# 604571; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:58:06.283588+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: TAPBP.","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:57:31.421543+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAPBP as ready","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:57:31.412478+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tapbp has been classified as Red List (Low Evidence).","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:57:28.591986+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAPBP were changed from  to Bare lymphocyte syndrome, type I, MIM# 604571","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:57:05.384012+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAPBP were set to ","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:56:40.659932+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAPBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:56:17.066961+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAPBP as Red List (low evidence)","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:56:17.058167+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tapbp has been classified as Red List (Low Evidence).","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:55:47.583749+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAPBP: Rating: RED; Mode of pathogenicity: None; Publications: 12149238; Phenotypes: Bare lymphocyte syndrome, type I, MIM# 604571; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAPBP","entity_type":"gene"},{"created":"2020-04-11T20:21:22.808701+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SH3BP2 were changed from Cherubism, MIM# 118400 to Cherubism, MIM# 118400","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:21:14.791345+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SH3BP2 as ready","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:21:14.781468+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sh3bp2 has been classified as Red List (Low Evidence).","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:21:00.222115+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SH3BP2 were changed from Cherubism, MIM# 118400 to Cherubism, MIM# 118400","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:20:39.565873+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SH3BP2 were changed from  to Cherubism, MIM# 118400","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:19:52.549732+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SH3BP2 were set to ","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:19:28.341069+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SH3BP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:18:52.250698+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SH3BP2 as Red List (low evidence)","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:18:52.237298+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sh3bp2 has been classified as Red List (Low Evidence).","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:18:22.005813+10:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SH3BP2: Rating: RED; Mode of pathogenicity: None; Publications: 26152156, 25705883, 25470448, 25220465; Phenotypes: Cherubism, MIM# 118400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SH3BP2","entity_type":"gene"},{"created":"2020-04-11T20:08:25.736618+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2135","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SEMA3E as ready","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T20:08:25.727957+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2135","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3e has been classified as Amber List (Moderate Evidence).","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:42:59.760950+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2135","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SEMA3E were changed from  to CHARGE syndrome, MIM#214800","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:42:40.612696+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2134","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SEMA3E were set to ","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:42:17.193785+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2133","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SEMA3E was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:42:11.067892+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2133","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SEMA3E as Amber List (moderate evidence)","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:42:11.059109+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2133","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3e has been classified as Amber List (Moderate Evidence).","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:41:50.803055+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2132","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SEMA3E: Rating: AMBER; Mode of pathogenicity: None; Publications: 15235037, 31691538, 31464029; Phenotypes: CHARGE syndrome, MIM#214800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:40:21.504905+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SEMA3E as ready","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:40:21.491597+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3e has been classified as Red List (Low Evidence).","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:40:18.591589+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SEMA3E were changed from  to CHARGE syndrome, MIM# 214800","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:39:54.824645+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SEMA3E were set to ","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:39:10.601799+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SEMA3E was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:38:41.219556+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SEMA3E as Red List (low evidence)","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:38:41.210668+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sema3e has been classified as Red List (Low Evidence).","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:38:08.676746+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SEMA3E: Rating: RED; Mode of pathogenicity: None; Publications: 15235037, 28634005; Phenotypes: CHARGE syndrome, MIM# 214800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2020-04-11T19:32:03.519010+10:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SAMD9 as ready","entity_name":"SAMD9","entity_type":"gene"},{"created":"2020-04-11T19:32:03.505479+10:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: samd9 has been classified as Green List (High Evidence).","entity_name":"SAMD9","entity_type":"gene"},{"created":"2020-04-11T19:31:59.672501+10:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SAMD9 were changed from  to MIRAGE syndrome, MIM# 617053","entity_name":"SAMD9","entity_type":"gene"},{"created":"2020-04-11T19:31:30.178903+10:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SAMD9 were set to ","entity_name":"SAMD9","entity_type":"gene"},{"created":"2020-04-11T19:30:59.841607+10:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SAMD9 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SAMD9","entity_type":"gene"},{"created":"2020-04-11T19:30:28.316112+10:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SAMD9: Rating: GREEN; Mode of pathogenicity: None; Publications: 31620126; Phenotypes: MIRAGE syndrome, MIM# 617053; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SAMD9","entity_type":"gene"},{"created":"2020-04-11T18:46:29.547367+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2132","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNF31 as ready","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:46:29.534496+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2132","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf31 has been classified as Amber List (Moderate Evidence).","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:46:20.363350+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2132","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RNF31 were changed from  to Immune deficiency; Autoinflammation","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:46:00.480845+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2131","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RNF31 were set to ","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:45:45.591283+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2130","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RNF31 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:45:32.048098+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2129","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RNF31 as Amber List (moderate evidence)","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:45:32.034968+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2129","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf31 has been classified as Amber List (Moderate Evidence).","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:45:13.359150+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2128","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RNF31: Rating: AMBER; Mode of pathogenicity: None; Publications: 26008899, 30936877; Phenotypes: Immune deficiency, Autoinflammation; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:44:25.354346+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNF31 as ready","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:44:25.344861+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf31 has been classified as Amber List (Moderate Evidence).","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:44:22.625032+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RNF31 were changed from  to Immune deficiency; Autoinflammation","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:43:59.111242+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RNF31 were set to ","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:43:35.354676+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RNF31 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:43:11.591691+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RNF31 as Amber List (moderate evidence)","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:43:11.581582+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnf31 has been classified as Amber List (Moderate Evidence).","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:42:40.791548+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RNF31: Rating: AMBER; Mode of pathogenicity: None; Publications: 26008899, 30936877; Phenotypes: Immune deficiency, Autoinflammation; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RNF31","entity_type":"gene"},{"created":"2020-04-11T18:39:28.790653+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2128","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RHOH as ready","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:39:28.775884+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2128","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rhoh has been classified as Red List (Low Evidence).","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:39:06.909838+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2128","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RHOH were changed from  to {?Epidermodysplasia verruciformis, susceptibility to, 4}, MIM# 618307","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:38:45.152892+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2127","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RHOH were set to ","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:38:31.448321+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2126","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RHOH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:38:17.128680+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2125","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RHOH as Red List (low evidence)","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:38:17.120060+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2125","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rhoh has been classified as Red List (Low Evidence).","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:37:49.699222+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2124","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RHOH: Rating: RED; Mode of pathogenicity: None; Publications: 22850876, 27574848; Phenotypes: {?Epidermodysplasia verruciformis, susceptibility to, 4}, MIM# 618307; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:37:40.689285+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RHOH as ready","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:37:40.675898+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rhoh has been classified as Red List (Low Evidence).","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:36:53.055241+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2124","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PSMB9 as ready","entity_name":"PSMB9","entity_type":"gene"},{"created":"2020-04-11T18:36:53.046627+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2124","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: psmb9 has been classified as Amber List (Moderate Evidence).","entity_name":"PSMB9","entity_type":"gene"},{"created":"2020-04-11T18:36:45.334011+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RHOH were changed from  to {?Epidermodysplasia verruciformis, susceptibility to, 4}, MIM# 618307","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:36:17.487715+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RHOH were set to ","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:35:43.614762+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RHOH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:35:15.687345+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RHOH as Red List (low evidence)","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:35:15.678430+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rhoh has been classified as Red List (Low Evidence).","entity_name":"RHOH","entity_type":"gene"},{"created":"2020-04-11T18:34:45.414989+10:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RHOH: Rating: RED; Mode of pathogenicity: None; Publications: 22850876, 27574848; Phenotypes: {?Epidermodysplasia verruciformis, susceptibility to, 4}, MIM# 618307; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RHOH","entity_type":"gene"}]}