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{
"count": 221415,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=525",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=523",
"results": [
{
"created": "2023-11-03T16:07:14.265011+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AUH was added\ngene: AUH was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AUH was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AUH were set to 3-methylglutaconic aciduria, type I, 250950 (3)",
"entity_name": "AUH",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:14.103868+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ATRX was added\ngene: ATRX was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ATRX was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: ATRX were set to Mental retardation-hypotonic facies syndrome, X-linked, 309580 (3)",
"entity_name": "ATRX",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:13.982411+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ATR was added\ngene: ATR was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ATR was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ATR were set to Seckel syndrome 1, 210600 (3)",
"entity_name": "ATR",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:13.863373+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ATP8B1 was added\ngene: ATP8B1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ATP8B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ATP8B1 were set to Cholestasis, progressive familial intrahepatic 1, 211600 (3)",
"entity_name": "ATP8B1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:13.694366+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ATP7B was added\ngene: ATP7B was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ATP7B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ATP7B were set to 28433102\nPhenotypes for gene: ATP7B were set to Wilson disease, 277900 (3)",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:13.580122+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ATP7A was added\ngene: ATP7A was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ATP7A was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: ATP7A were set to Menkes disease, 309400 (3)",
"entity_name": "ATP7A",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:13.467398+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ATP6V1B1 was added\ngene: ATP6V1B1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ATP6V1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ATP6V1B1 were set to Renal tubular acidosis with deafness, 267300 (3)",
"entity_name": "ATP6V1B1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:13.297889+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ATM was added\ngene: ATM was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ATM was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ATM were set to Ataxia-telangiectasia, 208900 (3)",
"entity_name": "ATM",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:13.185444+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ASS1 was added\ngene: ASS1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ASS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ASS1 were set to Citrullinemia, 215700 (3)",
"entity_name": "ASS1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:13.061664+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ASPM was added\ngene: ASPM was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ASPM was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ASPM were set to Microcephaly 5, primary, autosomal recessive, 608716 (3)",
"entity_name": "ASPM",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:12.894802+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ASPA was added\ngene: ASPA was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ASPA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ASPA were set to Canavan disease, 271900 (3)",
"entity_name": "ASPA",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:12.776976+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ASNS was added\ngene: ASNS was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ASNS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ASNS were set to Asparagine synthetase deficiency, 615574 (3)",
"entity_name": "ASNS",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:12.662061+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ASL was added\ngene: ASL was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ASL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ASL were set to Argininosuccinic aciduria, 207900 (3)",
"entity_name": "ASL",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:12.499043+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ARX was added\ngene: ARX was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ARX was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: ARX were set to Hydranencephaly with abnormal genitalia, 300215 (3)",
"entity_name": "ARX",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:12.388451+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ARSB was added\ngene: ARSB was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ARSB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARSB were set to Mucopolysaccharidosis type VI (Maroteaux-Lamy), 253200 (3)",
"entity_name": "ARSB",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:12.276729+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ARSA was added\ngene: ARSA was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ARSA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARSA were set to Metachromatic leukodystrophy, 250100 (3)",
"entity_name": "ARSA",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:12.159783+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ARL6 was added\ngene: ARL6 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ARL6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARL6 were set to Bardet-Biedl syndrome 3, 600151 (3)",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:11.994892+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ARL13B was added\ngene: ARL13B was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ARL13B was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARL13B were set to Joubert syndrome 8, 612291 (3)",
"entity_name": "ARL13B",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:11.885570+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ARG1 was added\ngene: ARG1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ARG1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARG1 were set to Argininemia, 207800 (3)",
"entity_name": "ARG1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:11.764222+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AQP2 was added\ngene: AQP2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AQP2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AQP2 were set to Diabetes insipidus, nephrogenic, 125800 (3)",
"entity_name": "AQP2",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:11.594711+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AP1S2 was added\ngene: AP1S2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AP1S2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: AP1S2 were set to Mental retardation, X-linked syndromic 5, 304340 (3)",
"entity_name": "AP1S2",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:11.475269+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AMT was added\ngene: AMT was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AMT was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AMT were set to Glycine encephalopathy, 605899 (3)",
"entity_name": "AMT",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:11.328499+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AMPD2 was added\ngene: AMPD2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AMPD2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AMPD2 were set to Pontocerebellar hypoplasia, type 9, 615809 (3)",
"entity_name": "AMPD2",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:11.190899+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALPL was added\ngene: ALPL was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALPL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALPL were set to Hypophosphatasia, infantile, 241500 (3)",
"entity_name": "ALPL",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:11.070147+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALMS1 was added\ngene: ALMS1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALMS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALMS1 were set to Alstrom syndrome, 203800 (3)",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:10.898511+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALG6 was added\ngene: ALG6 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALG6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALG6 were set to Congenital disorder of glycosylation, type Ic, 603147 (3)",
"entity_name": "ALG6",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:10.780558+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALG3 was added\ngene: ALG3 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALG3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALG3 were set to Congenital disorder of glycosylation, type Id, 601110 (3)",
"entity_name": "ALG3",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:10.617122+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALG1 was added\ngene: ALG1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALG1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALG1 were set to Congenital disorder of glycosylation, type Ik, 608540 (3)",
"entity_name": "ALG1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:10.494689+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALDOB was added\ngene: ALDOB was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALDOB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALDOB were set to Fructose intolerance, 229600 (3)",
"entity_name": "ALDOB",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:10.314443+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALDH7A1 was added\ngene: ALDH7A1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALDH7A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALDH7A1 were set to Epilepsy, pyridoxine-dependent, 266100 (3)",
"entity_name": "ALDH7A1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:10.191122+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALDH5A1 was added\ngene: ALDH5A1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALDH5A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALDH5A1 were set to Succinic semialdehyde dehydrogenase deficiency, 271980 (3)",
"entity_name": "ALDH5A1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:10.063405+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALDH3A2 was added\ngene: ALDH3A2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALDH3A2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALDH3A2 were set to Sjogren-Larsson syndrome, 270200 (3)",
"entity_name": "ALDH3A2",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:09.915469+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ALDH18A1 was added\ngene: ALDH18A1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ALDH18A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALDH18A1 were set to Spastic paraplegia 9B, autosomal recessive, 616586 (3)",
"entity_name": "ALDH18A1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:09.797554+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AK2 was added\ngene: AK2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AK2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AK2 were set to Reticular dysgenesis, 267500 (3)",
"entity_name": "AK2",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:09.677950+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AIPL1 was added\ngene: AIPL1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AIPL1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AIPL1 were set to Cone-rod dystrophy, 604393 (3)",
"entity_name": "AIPL1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:09.565918+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AIFM1 was added\ngene: AIFM1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AIFM1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: AIFM1 were set to Cowchock syndrome, 310490 (3)",
"entity_name": "AIFM1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:09.441606+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AHI1 was added\ngene: AHI1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AHI1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AHI1 were set to Joubert syndrome-3, 608629 (3)",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:09.273905+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AGXT was added\ngene: AGXT was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AGXT was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AGXT were set to Hyperoxaluria, primary, type 1, 259900 (3)",
"entity_name": "AGXT",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:09.126158+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AGPS was added\ngene: AGPS was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AGPS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AGPS were set to Chondrodysplasia punctata, rhizomelic, type 3, 600121 (3)",
"entity_name": "AGPS",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:08.992782+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AGL was added\ngene: AGL was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AGL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AGL were set to Glycogen storage disease IIIa, 232400 (3)",
"entity_name": "AGL",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:08.876041+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AGK was added\ngene: AGK was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AGK was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AGK were set to Sengers syndrome, 212350 (3)",
"entity_name": "AGK",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:08.714181+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AGA was added\ngene: AGA was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AGA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AGA were set to Aspartylglucosaminuria, 208400 (3)",
"entity_name": "AGA",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:08.581134+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ADSL was added\ngene: ADSL was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ADSL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ADSL were set to Adenylosuccinase deficiency, 103050 (3)",
"entity_name": "ADSL",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:08.458151+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ADGRV1 was added\ngene: ADGRV1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ADGRV1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ADGRV1 were set to Usher syndrome, type 2C, 605472 (3)",
"entity_name": "ADGRV1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:08.304499+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ADGRG1 was added\ngene: ADGRG1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ADGRG1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ADGRG1 were set to Polymicrogyria, bilateral frontoparietal, 606854 (3)",
"entity_name": "ADGRG1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:08.198514+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ADAR was added\ngene: ADAR was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ADAR was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ADAR were set to Aicardi-Goutieres syndrome 6, 615010 (3)",
"entity_name": "ADAR",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:08.080505+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ADAMTS2 was added\ngene: ADAMTS2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ADAMTS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ADAMTS2 were set to Ehlers-Danlos syndrome, type VIIC, 225410 (3)",
"entity_name": "ADAMTS2",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:07.962321+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ADA was added\ngene: ADA was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ADA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ADA were set to Adenosine deaminase deficiency, partial, 102700 (3)",
"entity_name": "ADA",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:07.803271+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ACOX1 was added\ngene: ACOX1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ACOX1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ACOX1 were set to Peroxisomal acyl-CoA oxidase deficiency, 264470 (3)",
"entity_name": "ACOX1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:07.684198+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ACAT1 was added\ngene: ACAT1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ACAT1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ACAT1 were set to Alpha-methylacetoacetic aciduria, 203750 (3)",
"entity_name": "ACAT1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:07.596631+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ACADVL was added\ngene: ACADVL was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ACADVL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ACADVL were set to VLCAD deficiency, 201475 (3)",
"entity_name": "ACADVL",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:07.462441+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ACADM was added\ngene: ACADM was added to Prepair 500+. Sources: Expert Review,Expert Review Green\nMode of inheritance for gene: ACADM was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ACADM were set to Acyl-CoA dehydrogenase, medium chain, deficiency of, MIM #201450",
"entity_name": "ACADM",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:07.334541+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ACAD9 was added\ngene: ACAD9 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ACAD9 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ACAD9 were set to Mitochondrial complex I deficiency due to ACAD9 deficiency, 611126 (3)",
"entity_name": "ACAD9",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:07.209203+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ABCD1 was added\ngene: ABCD1 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ABCD1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: ABCD1 were set to Adrenoleukodystrophy, 300100 (3)",
"entity_name": "ABCD1",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:07.084665+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ABCC8 was added\ngene: ABCC8 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ABCC8 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABCC8 were set to Hyperinsulinemic hypoglycemia, familial, 1, 256450 (3)",
"entity_name": "ABCC8",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:06.963655+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ABCB4 was added\ngene: ABCB4 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ABCB4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABCB4 were set to Cholestasis, progressive familial intrahepatic 3, 602347 (3)",
"entity_name": "ABCB4",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:06.802237+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ABCB11 was added\ngene: ABCB11 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ABCB11 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABCB11 were set to Cholestasis, progressive familial intrahepatic 2, 601847 (3)",
"entity_name": "ABCB11",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:06.694933+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ABCA3 was added\ngene: ABCA3 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ABCA3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABCA3 were set to Surfactant metabolism dysfunction, pulmonary, 3, 610921 (3)",
"entity_name": "ABCA3",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:06.567912+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: ABCA12 was added\ngene: ABCA12 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: ABCA12 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABCA12 were set to Ichthyosis, congenital, autosomal recessive 4A, 601277 (3)",
"entity_name": "ABCA12",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:06.434210+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AARS2 was added\ngene: AARS2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AARS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AARS2 were set to Combined oxidative phosphorylation deficiency 8, 614096 (3)",
"entity_name": "AARS2",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:06.293641+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "gene: AAAS was added\ngene: AAAS was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green\nMode of inheritance for gene: AAAS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AAAS were set to Achalasia-addisonianism-alacrimia syndrome, 231550 (3)",
"entity_name": "AAAS",
"entity_type": "gene"
},
{
"created": "2023-11-03T16:07:06.208825+11:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "0.0",
"user_name": "Seb Lunke",
"item_type": "panel",
"text": "Added panel Prepair 500+",
"entity_name": null,
"entity_type": null
},
{
"created": "2023-11-03T11:58:07.584589+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FMNL2 as ready",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-03T11:58:07.570356+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fmnl2 has been classified as Red List (Low Evidence).",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-03T11:57:59.284350+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FMNL2 was added\ngene: FMNL2 was added to Inflammatory bowel disease. Sources: Literature\nMode of inheritance for gene: FMNL2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: FMNL2 were set to 34043722\nPhenotypes for gene: FMNL2 were set to inflammatory bowel disease, MONDO:0005265, FMNL2-related\nReview for gene: FMNL2 was set to RED\nAdded comment: A patient was reported with a de novo heterozygous FMNL2 variant (p.Leu136Pro) and with severe very early onset inflammatory bowel disease (IBD). The functional characterisation of this variant showed that FMNL2 L136P protein displayed subcellular mislocalisation and deregulated protein autoinhibition indicating gain-of-function mechanism (PMID:34043722). \nSources: Literature",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-03T11:56:22.331539+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FMNL2 as ready",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-03T11:56:22.320129+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fmnl2 has been classified as Red List (Low Evidence).",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-03T11:56:14.516743+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FMNL2 were changed from inflammatory bowel disease, MONDO:0005265 to inflammatory bowel disease, MONDO:0005265, FMNL2-related",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-03T11:54:43.591209+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1352",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FMNL2 as Red List (low evidence)",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-03T11:54:43.569054+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1352",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fmnl2 has been classified as Red List (Low Evidence).",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-03T02:14:48.195537+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1351",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "gene: FMNL2 was added\ngene: FMNL2 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: FMNL2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: FMNL2 were set to 34043722\nPhenotypes for gene: FMNL2 were set to inflammatory bowel disease, MONDO:0005265\nMode of pathogenicity for gene: FMNL2 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments\nReview for gene: FMNL2 was set to AMBER\nAdded comment: A patient was reported with a de novo heterozygous FMNL2 variant (p.Leu136Pro) and with severe very early onset inflammatory bowel disease (IBD). The functional characterisation of this variant showed that FMNL2 L136P protein displayed subcellular mislocalisation and deregulated protein autoinhibition indicating gain-of-function mechanism (PMID:34043722). \nSources: Literature",
"entity_name": "FMNL2",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:03:28.123419+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5607",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HIST1H4J were set to 31804630",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:02:34.087158+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H4J as ready",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:02:34.083131+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: New gene name: H4C11",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:02:34.064528+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h4j has been classified as Amber List (Moderate Evidence).",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:02:19.806512+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: HIST1H4J.",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:01:50.381714+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1351",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: HIST1H4J were set to 31804630",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:01:27.480331+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H4J as ready",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:01:27.476488+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: New gene name: H4C11",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:01:27.456263+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h4j has been classified as Amber List (Moderate Evidence).",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:00:54.237224+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: HIST1H4J.",
"entity_name": "HIST1H4J",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:00:15.541822+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H4I as ready",
"entity_name": "HIST1H4I",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:00:15.532866+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: New gene name: H4C9",
"entity_name": "HIST1H4I",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:00:15.472923+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h4i has been classified as Green List (High Evidence).",
"entity_name": "HIST1H4I",
"entity_type": "gene"
},
{
"created": "2023-11-02T20:00:00.623536+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: HIST1H4I.",
"entity_name": "HIST1H4I",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:59:34.172434+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H4I as ready",
"entity_name": "HIST1H4I",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:59:34.167352+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: New gene name: H4C9",
"entity_name": "HIST1H4I",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:59:34.111530+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h4i has been classified as Green List (High Evidence).",
"entity_name": "HIST1H4I",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:58:57.450598+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: HIST1H4I.",
"entity_name": "HIST1H4I",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:58:18.250570+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H4F as ready",
"entity_name": "HIST1H4F",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:58:18.238639+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: New gene name H4C6",
"entity_name": "HIST1H4F",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:58:18.133876+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h4f has been classified as Amber List (Moderate Evidence).",
"entity_name": "HIST1H4F",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:57:56.110194+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: HIST1H4F.",
"entity_name": "HIST1H4F",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:57:02.129855+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H4F as ready",
"entity_name": "HIST1H4F",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:57:02.120221+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: New gene name H4C6",
"entity_name": "HIST1H4F",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:57:02.069150+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hist1h4f has been classified as Amber List (Moderate Evidence).",
"entity_name": "HIST1H4F",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:56:29.672113+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: HIST1H4F.",
"entity_name": "HIST1H4F",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:55:27.980156+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: HIST1H4E.",
"entity_name": "HIST1H4E",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:54:48.066493+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: HIST1H4D.",
"entity_name": "HIST1H4D",
"entity_type": "gene"
},
{
"created": "2023-11-02T19:54:22.381087+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HIST1H4D as ready",
"entity_name": "HIST1H4D",
"entity_type": "gene"
}
]
}