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{
"count": 220488,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=970",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=968",
"results": [
{
"created": "2022-02-24T10:00:33.966966+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SPEG: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Centronuclear myopathy 5, MIM# 615959; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:58:50.877841+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPG11 as ready",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:58:50.867894+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spg11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:58:46.541825+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SPG11 were changed from SPASTIC PARAPLEGIA-11 to Spastic paraplegia 11, autosomal recessive, MIM# 604360",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:58:29.452568+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPG11 were set to ",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:58:15.439968+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SPG11 as Amber List (moderate evidence)",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:58:15.429140+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spg11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:58:02.460530+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SPG11: Changed rating: AMBER",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:57:55.987158+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Bi-alllelic variants in this gene also cause spastic paraplegia-11 (OMIM# 604360) but also juvenile amyotrophic lateral sclerosis-5 (OMIM# 602099), and CMT2X. Same variants have been reported in association with different phenotypes, poor genotype-phenotype correlation.\r\n\r\nRecent review of >300 individuals with SPG11-related disease. Mean age at onset was 13.10 ± 3.65 years, with initial symptoms like gait disturbance (107/195, 54.87%) and intellectual disability (47/195, 24.10%). Cognitive decline (228/270, 84.44%) was the most common complex manifestation stepped by dysarthria (134/195, 68.72%), neuropathy (112/177, 63.28%), amyatrophy, sphincter disturbance (60/130, 46.15%) and ataxia (90/194, 46.39%).; to: Bi-alllelic variants in this gene also cause spastic paraplegia-11 (OMIM# 604360) but also juvenile amyotrophic lateral sclerosis-5 (OMIM# 602099), and CMT2X. Same variants have been reported in association with different phenotypes, poor genotype-phenotype correlation.\r\n\r\nRecent review of >300 individuals with SPG11-related disease. Mean age at onset was 13.10 ± 3.65 years, with initial symptoms like gait disturbance (107/195, 54.87%) and intellectual disability (47/195, 24.10%). Cognitive decline (228/270, 84.44%) was the most common complex manifestation stepped by dysarthria (134/195, 68.72%), neuropathy (112/177, 63.28%), amyatrophy, sphincter disturbance (60/130, 46.15%) and ataxia (90/194, 46.39%).\r\n\r\nAlthough onset of clinical features is typically in childhood or later, absent CC/CC abnormalities reported.",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:55:23.952414+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPRED1 as ready",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:55:23.940806+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spred1 has been classified as Red List (Low Evidence).",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:55:18.973179+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SPRED1 were changed from LEGIUS SYNDROME to Legius syndrome, MIM# 611431",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:55:05.817774+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPRED1 were set to ",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:54:46.205798+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SPRED1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:54:36.181851+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SPRED1 as Red List (low evidence)",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:54:36.170094+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spred1 has been classified as Red List (Low Evidence).",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:54:21.999858+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Multiple affected individuals reported, deletions account for ~10% of causative variants. Legius syndrome is characterised by multiple cafe-au-lait spots, sometimes associated with skin fold freckling, variable dysmorphic features such as hypertelorism or macrocephaly, lipomas, and mild learning disabilities or attention problems. It is not associated with neurofibromas, optic gliomas, Lisch nodules, or tumor predisposition. The SPRED1 gene encodes a negative regulator of the RAS-MAPK pathway, similar to neurofibromin.; to: Multiple affected individuals reported, deletions account for ~10% of causative variants. Legius syndrome is characterised by multiple cafe-au-lait spots, sometimes associated with skin fold freckling, variable dysmorphic features such as hypertelorism or macrocephaly, lipomas, and mild learning disabilities or attention problems. It is not associated with neurofibromas, optic gliomas, Lisch nodules, or tumor predisposition. The SPRED1 gene encodes a negative regulator of the RAS-MAPK pathway, similar to neurofibromin.\r\n\r\nClinical presentation is typically post-natal.",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:54:02.807019+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SPRED1: Changed rating: RED",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:46:02.607122+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SRCAP as ready",
"entity_name": "SRCAP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:46:02.553142+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: srcap has been classified as Green List (High Evidence).",
"entity_name": "SRCAP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:45:56.958567+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SRCAP were changed from FLOATING-HARBOR SYNDROME to Floating-Harbor syndrome, MIM# 136140",
"entity_name": "SRCAP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:45:42.877916+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SRCAP were set to ",
"entity_name": "SRCAP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:45:31.569517+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SRCAP was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SRCAP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:45:17.885471+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SRCAP: Added comment: IUGR and multiple congenital anomalies.; Changed phenotypes: Floating-Harbor syndrome, MIM# 136140",
"entity_name": "SRCAP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:28:09.455820+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SRD5A3 as ready",
"entity_name": "SRD5A3",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:28:09.445181+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: srd5a3 has been classified as Green List (High Evidence).",
"entity_name": "SRD5A3",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:28:05.523592+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SRD5A3 were changed from CONGENITAL DISORDERS OF GLYCOSYLATION to Congenital disorder of glycosylation, type Iq, MIM# 612379; Kahrizi syndrome, MIM# 612713",
"entity_name": "SRD5A3",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:27:52.565326+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SRD5A3 were set to ",
"entity_name": "SRD5A3",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:26:05.215698+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STAG2 as ready",
"entity_name": "STAG2",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:26:05.203804+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stag2 has been classified as Green List (High Evidence).",
"entity_name": "STAG2",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:25:59.779167+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STAG2 were changed from STAG2-related developmental delay with microcephaly and congenital anomalies to Mullegama-Klein-Martinez syndrome, MIM#\t301022; Holoprosencephaly 13, X-linked, MIM#\t301043",
"entity_name": "STAG2",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:23:03.265978+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STAG2 were set to 29263825; 28296084; 30158690",
"entity_name": "STAG2",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:22:08.786003+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STAMBP as ready",
"entity_name": "STAMBP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:22:08.773276+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stambp has been classified as Green List (High Evidence).",
"entity_name": "STAMBP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:22:03.106729+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STAMBP were changed from MICROCEPHALY CAPILLARY MALFORMATION (MIC-CAP) SYNDROME to Microcephaly-capillary malformation syndrome, MIM# 614261; MONDO:0013659",
"entity_name": "STAMBP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:21:48.835528+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STAMBP were set to ",
"entity_name": "STAMBP",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:21:11.671767+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STRA6 as ready",
"entity_name": "STRA6",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:21:11.658099+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stra6 has been classified as Green List (High Evidence).",
"entity_name": "STRA6",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:21:07.950067+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STRA6 were changed from MICROPHTHALMIA SYNDROMIC TYPE 9 to Microphthalmia, syndromic 9, MIM# 601186",
"entity_name": "STRA6",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:20:52.573466+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STRA6 were set to ",
"entity_name": "STRA6",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:20:13.220729+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SUMF1 as ready",
"entity_name": "SUMF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:20:13.208370+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sumf1 has been classified as Green List (High Evidence).",
"entity_name": "SUMF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:20:09.277633+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SUMF1 were changed from SULFATIDOSIS, JUVENILE, AUSTIN TYPE to Multiple sulfatase deficiency, MIM# 272200",
"entity_name": "SUMF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:19:55.580697+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SUMF1 were set to ",
"entity_name": "SUMF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:19:38.781363+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Single case report found of hydrops in this metabolic condition. \nSources: Expert list; to: Single case report found of hydrops in this metabolic condition. Hydrocephalus and structural brain abnormalities reported.\r\n\r\nSources: Expert list",
"entity_name": "SUMF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:19:21.631442+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SUMF1: Changed rating: GREEN; Changed phenotypes: Multiple sulfatase deficiency, MIM# 272200",
"entity_name": "SUMF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:18:12.398126+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SUZ12 as ready",
"entity_name": "SUZ12",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:18:12.387524+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: suz12 has been classified as Green List (High Evidence).",
"entity_name": "SUZ12",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:18:05.696348+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SUZ12 were changed from Weaver-like overgrowth syndrome; Imagawa-Matsumoto syndrome #618786 to Imagawa-Matsumoto syndrome #618786",
"entity_name": "SUZ12",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:17:54.752714+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SUZ12 were set to 30019515; 28229514",
"entity_name": "SUZ12",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:17:37.163259+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SUZ12 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SUZ12",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:17:24.327982+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Thirteen individuals from 12 families.; to: Thirteen individuals from 12 families. Overgrowth of prenatal onset, brain abnormalities reported in some.",
"entity_name": "SUZ12",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:14:40.107754+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAF1 as ready",
"entity_name": "TAF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:14:40.098205+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: taf1 has been classified as Green List (High Evidence).",
"entity_name": "TAF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:14:36.614418+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAF1 were changed from Dysmorphic Features, Intellectual Disability, and Neurological Manifestations to Mental retardation, X-linked, syndromic 33, MIM# 300966",
"entity_name": "TAF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:14:16.767349+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TAF1 were set to ",
"entity_name": "TAF1",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:13:20.430867+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAZ as ready",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:13:20.418583+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: taz has been classified as Green List (High Evidence).",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:13:15.988697+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAZ were changed from BARTH SYNDROME to Barth syndrome, MIM#302060",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:13:03.727679+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TAZ were set to ",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:12:22.333622+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D20 as ready",
"entity_name": "TBC1D20",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:12:22.322081+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d20 has been classified as Green List (High Evidence).",
"entity_name": "TBC1D20",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:12:18.423375+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D20 were changed from Warburg micro syndrome 4; Warburg micro syndrome 4 615663 to Warburg micro syndrome 4, MIM# 615663",
"entity_name": "TBC1D20",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:11:25.394207+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBCD as ready",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:11:25.384293+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbcd has been classified as Green List (High Evidence).",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:11:18.325900+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBCD were set to ",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:11:01.811723+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: CC abnormalities.; to: CC abnormalities, arthrogryposis are relevant to fetal panel.",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2022-02-24T09:10:05.609241+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: TBCD: CC abnormalities.",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:34:04.823056+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBX1 as ready",
"entity_name": "TBX1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:34:04.813188+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbx1 has been classified as Green List (High Evidence).",
"entity_name": "TBX1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:34:01.097398+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBX1 were changed from 22Q11.2 DELETION SYNDROME to DiGeorge syndrome, MIM# 188400",
"entity_name": "TBX1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:33:47.822681+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4099",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBX1 were set to ",
"entity_name": "TBX1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:33:36.303845+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4098",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: TBX1 was changed from to None",
"entity_name": "TBX1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:33:26.172820+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4097",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBX1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:32:52.685626+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4096",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBX3 as ready",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:32:52.673013+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4096",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbx3 has been classified as Green List (High Evidence).",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:32:48.990009+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4096",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBX3 were changed from ULNAR-MAMMARY SYNDROME to Ulnar-mammary syndrome, MIM# 181450; MONDO:0008411",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:32:36.886719+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4095",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBX3 were set to ",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:32:25.166488+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4094",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBX3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:31:55.130089+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4093",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBX5 as ready",
"entity_name": "TBX5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:31:55.119854+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4093",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbx5 has been classified as Green List (High Evidence).",
"entity_name": "TBX5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:31:51.530299+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4093",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBX5 were changed from HOLT-ORAM SYNDROME to Holt-Oram syndrome, MIM# 142900",
"entity_name": "TBX5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:31:39.938531+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4092",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBX5 were set to ",
"entity_name": "TBX5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:31:29.517148+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4091",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBX5 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:30:59.734727+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4090",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCF4 as ready",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:30:59.721848+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4090",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcf4 has been classified as Green List (High Evidence).",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:30:55.888608+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4090",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCF4 were changed from PITT-HOPKINS SYNDROME to Pitt-Hopkins syndrome, MIM# 610954",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:30:36.588500+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4089",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCF4 were set to ",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:30:24.088760+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4088",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TCF4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TCF4",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:29:56.853631+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4087",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCIRG1 as ready",
"entity_name": "TCIRG1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:29:56.843744+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4087",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcirg1 has been classified as Green List (High Evidence).",
"entity_name": "TCIRG1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:29:22.599262+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4087",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCTN1 as ready",
"entity_name": "TCTN1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:29:22.587956+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4087",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tctn1 has been classified as Green List (High Evidence).",
"entity_name": "TCTN1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:29:19.325821+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4087",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCTN1 were changed from Joubert syndrome 13 614173; JOUBERT SYNDROME AND RELATED DISORDERS to Joubert syndrome 13, MIM# 614173",
"entity_name": "TCTN1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:29:07.555395+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4086",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCTN1 were set to ",
"entity_name": "TCTN1",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:28:27.719936+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4085",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCTN2 as ready",
"entity_name": "TCTN2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:28:27.696996+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4085",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tctn2 has been classified as Green List (High Evidence).",
"entity_name": "TCTN2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:28:23.995872+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4085",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCTN2 were changed from JOUBERT SYNDROME AND RELATED DISORDERS to Joubert syndrome 24, MIM# 616654; MONDO:0014724; Meckel syndrome 8, MIM# 613885; MONDO:0013482",
"entity_name": "TCTN2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:28:14.987009+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4084",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCTN2 were set to 30712880",
"entity_name": "TCTN2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:27:24.040295+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4083",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCTN3 as ready",
"entity_name": "TCTN3",
"entity_type": "gene"
}
]
}