HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220489,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=972",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=970",
"results": [
{
"created": "2022-02-23T16:43:29.781291+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIP12 as ready",
"entity_name": "TRIP12",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:43:29.771743+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trip12 has been classified as Red List (Low Evidence).",
"entity_name": "TRIP12",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:43:25.414709+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIP12 were changed from TRIP12-related intellectual disability with/without autism spectrum disorder to Mental retardation autosomal dominant 49, Clark-Baraitser Syndrome, MIM#617752",
"entity_name": "TRIP12",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:43:12.054302+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIP12 were set to ",
"entity_name": "TRIP12",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:42:56.873173+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIP12 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRIP12",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:42:47.424164+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIP12 as Red List (low evidence)",
"entity_name": "TRIP12",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:42:47.410087+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trip12 has been classified as Red List (Low Evidence).",
"entity_name": "TRIP12",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:42:34.200852+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRIP12: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation autosomal dominant 49, Clark-Baraitser Syndrome, MIM#617752; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRIP12",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:41:19.936649+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIP4 as ready",
"entity_name": "TRIP4",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:41:19.927938+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trip4 has been classified as Green List (High Evidence).",
"entity_name": "TRIP4",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:41:15.336330+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIP4 were changed from Prenatal-onset spinal muscular atrophy with congenital bone fractures, MONDO:0000209; Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome, MONDO:0014896; ?Muscular dystrophy, congenital, Davignon-Chauveau type, OMIM:617066; Spinal muscular atrophy with congenital bone fractures 1, OMIM:616866; Spinal muscular atrophy with congenital bone fractures 1, MONDO:0014806 to Spinal muscular atrophy with congenital bone fractures 1, OMIM:616866; Spinal muscular atrophy with congenital bone fractures 1, MONDO:0014806",
"entity_name": "TRIP4",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:39:16.946875+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSEN54 as ready",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:39:16.935944+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen54 has been classified as Green List (High Evidence).",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:39:12.495435+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN54 were changed from ?Pontocerebellar hypoplasia type 5, OMIM:610204; Pontocerebellar hypoplasia type 4, OMIM:225753; Pontocerebellar hypoplasia type 2A, OMIM:277470 to Pontocerebellar hypoplasia type 5, OMIM:610204; Pontocerebellar hypoplasia type 4, OMIM:225753; Pontocerebellar hypoplasia type 2A, OMIM:277470",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:38:55.866440+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4030",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSEN54 were set to 16470708; 20952379; 20956791",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:37:27.237371+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC21B as ready",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:37:27.226237+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc21b has been classified as Green List (High Evidence).",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:37:23.169243+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC21B were changed from Short-rib thoracic dysplasia 4 with or without polydactyly 613819 to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:36:18.813953+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4028",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC21B were set to ",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:35:37.511792+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC8 as ready",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:35:37.499791+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc8 has been classified as Green List (High Evidence).",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:35:33.339719+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC8 were changed from RETINITIS PIGMENTOSA TYPE 51; BARDET-BIEDL SYNDROME TYPE 8 to Bardet-Biedl syndrome 8, MIM# 615985",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:35:17.701689+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4026",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC8 were set to ",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:34:43.813335+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTN as ready",
"entity_name": "TTN",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:34:43.798111+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttn has been classified as Green List (High Evidence).",
"entity_name": "TTN",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:34:38.873820+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTN were changed from congenital titinopathy with arthrogryposis to Salih myopathy; Muscular dystrophy, limb-girdle, autosomal recessive 10",
"entity_name": "TTN",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:34:24.130942+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4024",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTN were set to 29575618; 28040389; 29691892",
"entity_name": "TTN",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:33:35.246729+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBB as ready",
"entity_name": "TUBB",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:33:35.236962+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb has been classified as Green List (High Evidence).",
"entity_name": "TUBB",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:33:30.473414+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBB were changed from CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; Circumferential Skin Creases Kunze Type to Cortical dysplasia, complex, with other brain malformations 6, MIM#615771",
"entity_name": "TUBB",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:33:16.752654+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4022",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBB were set to ",
"entity_name": "TUBB",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:33:04.410463+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4021",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBB was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TUBB",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:32:22.289744+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4020",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBB2A as ready",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:32:22.276360+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4020",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb2a has been classified as Green List (High Evidence).",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:32:17.597950+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4020",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBB2A were set to 28840640; 30016746; 25326637; 27770045; 24702957",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:32:02.813371+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4019",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBB2A was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:31:25.648305+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4018",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBB2B as ready",
"entity_name": "TUBB2B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:31:25.634125+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4018",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb2b has been classified as Green List (High Evidence).",
"entity_name": "TUBB2B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:31:20.811821+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4018",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBB2B were changed from POLYMICROGYRIA ASYMMETRIC to Cortical dysplasia, complex, with other brain malformations 7 MIM#610031",
"entity_name": "TUBB2B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:31:07.329661+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4017",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBB2B were set to ",
"entity_name": "TUBB2B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:30:21.331891+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBGCP6 as ready",
"entity_name": "TUBGCP6",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:30:21.321003+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubgcp6 has been classified as Green List (High Evidence).",
"entity_name": "TUBGCP6",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:30:17.379471+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBGCP6 were changed from MICROCEPHALY AND CHORIORETINOPATHY WITH OR WITHOUT MENTAL RETARDATION to Microcephaly and chorioretinopathy, autosomal recessive, 1, MIM#251270",
"entity_name": "TUBGCP6",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:30:02.698317+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4015",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBGCP6 were set to ",
"entity_name": "TUBGCP6",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:29:14.153419+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4014",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBA1 as ready",
"entity_name": "UBA1",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:29:14.143347+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4014",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uba1 has been classified as Green List (High Evidence).",
"entity_name": "UBA1",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:29:09.599765+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4014",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBA1 were changed from Spinal muscular atrophy, X-linked 2, infantile 301830 to Spinal muscular atrophy, X-linked 2, infantile, MIM# 301830",
"entity_name": "UBA1",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:28:56.079389+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4013",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBA1 were set to ",
"entity_name": "UBA1",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:28:00.663992+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4012",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBE3B as ready",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:28:00.624474+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4012",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ube3b has been classified as Green List (High Evidence).",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:27:53.901009+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4012",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBE3B were changed from BLEPHAROPHIMOSIS-MENTAL RETARDATION to Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:27:35.702033+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4011",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBE3B were set to ",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:27:18.112958+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4010",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Intellectual disability, microcephaly, dysmorphic features, including blepharophimosis and ptosis. Over 20 families reported.; to: Intellectual disability, microcephaly, dysmorphic features, including blepharophimosis and ptosis. Congenital heart disease. Over 20 families reported.",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:26:23.209880+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4010",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBR1 as ready",
"entity_name": "UBR1",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:26:23.199146+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4010",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ubr1 has been classified as Green List (High Evidence).",
"entity_name": "UBR1",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:26:19.076641+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4010",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBR1 were changed from JOHANSON-BLIZZARD SYNDROME to Johanson-Blizzard syndrome (MIM#243800)",
"entity_name": "UBR1",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:26:06.268477+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4009",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBR1 were set to ",
"entity_name": "UBR1",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:25:26.637883+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4008",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UMPS as ready",
"entity_name": "UMPS",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:25:26.614103+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4008",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: umps has been classified as Green List (High Evidence).",
"entity_name": "UMPS",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:25:12.046921+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4008",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UMPS were changed from OROTIC ACIDURIA TYPE 1 to Orotic aciduria MIM# 258900",
"entity_name": "UMPS",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:24:57.513682+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4007",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UMPS were set to ",
"entity_name": "UMPS",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:24:08.145011+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4006",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VIPAS39 as ready",
"entity_name": "VIPAS39",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:24:08.134619+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4006",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vipas39 has been classified as Green List (High Evidence).",
"entity_name": "VIPAS39",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:24:04.284235+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4006",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VIPAS39 were changed from ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 to Arthrogryposis, renal dysfunction, and cholestasis 2, OMIM #613404",
"entity_name": "VIPAS39",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:23:46.869441+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4005",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VIPAS39 were set to ",
"entity_name": "VIPAS39",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:23:30.468656+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4004",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: VIPAS39: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Arthrogryposis, renal dysfunction, and cholestasis 2, OMIM #613404; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "VIPAS39",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:22:40.253615+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4004",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VPS13B as ready",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:22:40.243669+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4004",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vps13b has been classified as Amber List (Moderate Evidence).",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:22:36.050026+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4004",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VPS13B were changed from COHEN SYNDROME to Cohen syndrome (MIM# 216550)",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:22:19.767424+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4003",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: VPS13B as Amber List (moderate evidence)",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:22:19.756067+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4003",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vps13b has been classified as Amber List (Moderate Evidence).",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:22:06.599635+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: VPS13B: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Cohen syndrome (MIM# 216550); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:20:25.694258+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VPS33B as ready",
"entity_name": "VPS33B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:20:25.683030+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vps33b has been classified as Green List (High Evidence).",
"entity_name": "VPS33B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:20:20.132445+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VPS33B were changed from ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 to Arthrogryposis, renal dysfunction, and cholestasis 1 (MIM#208085)",
"entity_name": "VPS33B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:20:06.499803+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4001",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VPS33B were set to ",
"entity_name": "VPS33B",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:19:28.926264+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VSX2 as ready",
"entity_name": "VSX2",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:19:28.914725+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vsx2 has been classified as Green List (High Evidence).",
"entity_name": "VSX2",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:18:21.480095+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VSX2 were changed from MICROPHTHALMIA ISOLATED TYPE 2; MICROPHTHALMIA WITH CATARACTS AND IRIS ABNORMALITIES; MICROPHTHALMIA ISOLATED WITH COLOBOMA TYPE 3 to Microphthalmia with coloboma 3, MIM# 610092; Microphthalmia, isolated 2, MIM# 610093",
"entity_name": "VSX2",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:18:02.131574+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VSX2 were set to ",
"entity_name": "VSX2",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:17:21.290518+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3998",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDPCP as ready",
"entity_name": "WDPCP",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:17:21.280961+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3998",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdpcp has been classified as Green List (High Evidence).",
"entity_name": "WDPCP",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:17:13.502367+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3998",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDPCP were changed from BARDET-BIEDL SYNDROME TYPE 15 to Bardet-Biedl syndrome 15, MIM# 615992; OFD; Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085",
"entity_name": "WDPCP",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:16:59.913387+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3997",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDPCP were set to ",
"entity_name": "WDPCP",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:16:07.947480+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR19 as ready",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:16:07.930024+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr19 has been classified as Green List (High Evidence).",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:15:49.110847+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR19 were changed from CRANIOECTODERMAL DYSPLASIA 4; ASPHYXIATING THORACIC DYSTROPHY 5 to Nephronophthisis 13, MIM# 614377; Senior-Loken syndrome 8, MIM# 616307; Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376; Cranioectodermal dysplasia 4, MIM# 614378",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:15:14.633951+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3995",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR19 were set to ",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:14:55.676978+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3994",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Variants in this gene are associated with a range of ciliopathies. Two families reported with a predominantly skeletal phenotype.; to: Variants in this gene are associated with a range of ciliopathies. ",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:14:45.867351+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3994",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: WDR19: Changed rating: GREEN; Changed publications: 33946315, 33875766, 33606107, 22019273, 23559409, 23683095, 32055034; Changed phenotypes: Nephronophthisis 13, MIM# 614377, Senior-Loken syndrome 8, MIM# 616307, Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376, Cranioectodermal dysplasia 4, MIM# 614378",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:51:03.440889+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3994",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D1 as ready",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:51:03.431789+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3994",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d1 has been classified as Green List (High Evidence).",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:50:57.095295+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3994",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TBC1D1 as Green List (high evidence)",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:50:57.085233+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3994",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d1 has been classified as Green List (High Evidence).",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:50:20.923122+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SRGAP1 as ready",
"entity_name": "SRGAP1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:50:20.901183+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: srgap1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SRGAP1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:50:13.426904+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SRGAP1 as Amber List (moderate evidence)",
"entity_name": "SRGAP1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:50:13.417424+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3993",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: srgap1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SRGAP1",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:49:44.492298+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3992",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLIT2 as ready",
"entity_name": "SLIT2",
"entity_type": "gene"
},
{
"created": "2022-02-23T15:49:44.479840+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3992",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slit2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLIT2",
"entity_type": "gene"
}
]
}