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{
"count": 220732,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=974",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=972",
"results": [
{
"created": "2022-02-23T18:08:03.110980+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4056",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM237 were set to ",
"entity_name": "TMEM237",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:07:31.975587+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4055",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM5 as ready",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:07:31.963768+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4055",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem5 has been classified as Green List (High Evidence).",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:07:24.751501+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4055",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM5 were changed from SEVERE COBBLESTONE LISSENCEPHALY to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, MIM# 615041, MONDO:0014022",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:07:12.884075+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4054",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM5 were set to ",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:06:41.080576+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4053",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM67 as ready",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:06:41.069368+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4053",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem67 has been classified as Green List (High Evidence).",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:06:37.317436+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4053",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM67 were changed from COACH SYNDROM; JOUBERT SYNDROME TYPE 6; MECKEL SYNDROME TYPE 3; NEPHRONOPHTHISIS TYPE 11 to Joubert syndrome 6, MIM# 610688; Meckel syndrome 3, MIM# 607361",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:06:24.920035+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM67 were set to ",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:05:50.899385+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM94 as ready",
"entity_name": "TMEM94",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:05:50.889570+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem94 has been classified as Green List (High Evidence).",
"entity_name": "TMEM94",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:05:13.314926+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TOP3A as ready",
"entity_name": "TOP3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:05:13.297722+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: top3a has been classified as Green List (High Evidence).",
"entity_name": "TOP3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:05:09.656064+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TOP3A were changed from Bloom Syndrome like Disorder to Microcephaly, growth restriction, and increased sister chromatid exchange 2, MIM# 618097",
"entity_name": "TOP3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:04:59.246133+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4050",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TOP3A were set to 30193137",
"entity_name": "TOP3A",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:04:25.506615+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TP63 as ready",
"entity_name": "TP63",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:04:25.492872+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tp63 has been classified as Green List (High Evidence).",
"entity_name": "TP63",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:04:22.211210+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TP63 were changed from ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE; ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME; ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFT LIP/PALATE SYNDROME TYPE 3; SPLIT-HAND/FOOT MALFORMATION TYPE 4; ECTODERMAL DYSPLASIA RAPP-HODGKIN TYPE; NON-SYNDROMIC OROFACIAL CLEFT TYPE 8; LIMB-MAMMARY SYNDROME to ADULT syndrome, OMIM #103285; Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3, OMIM #604292; Hay-Wells syndrome, OMIM #106260; Limb-mammary syndrome, OMIM #603543; Orofacial cleft 8, OMIM #618149; Rapp-Hodgkin syndrome, OMIM #129400; Split-hand/foot malformation 4, OMIM #605289",
"entity_name": "TP63",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:04:04.556081+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TP63 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TP63",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:03:45.161863+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TP63: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ADULT syndrome, OMIM #103285, Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3, OMIM #604292, Hay-Wells syndrome, OMIM #106260, Limb-mammary syndrome, OMIM #603543, Orofacial cleft 8, OMIM #618149, Rapp-Hodgkin syndrome, OMIM #129400, Split-hand/foot malformation 4, OMIM #605289; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TP63",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:03:05.711491+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TPM2 as ready",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:03:05.701955+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpm2 has been classified as Green List (High Evidence).",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:03:01.788674+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TPM2 were changed from Arthrogryposis multiplex congenita, distal, type 1, 108120; Arthrogryposis, distal, type 2B, 601680; ARTHROGRYPOSIS, DISTAL, TYPE 1 to Arthrogryposis multiplex congenita, distal, type 1, 108120; Arthrogryposis, distal, type 2B, 601680; Multiple pterygium syndrome",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:02:43.104587+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4046",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TPM2 were set to 12592607; 17339586",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:02:26.370472+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TPM2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:01:56.515195+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAF7 as ready",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:01:56.503637+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: traf7 has been classified as Green List (High Evidence).",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:01:52.764510+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAF7 were changed from Developmental Delay, Congenital Anomalies, and Dysmorphic Features; Cardiac, facial, and digital anomalies with developmental delay, 618164 to Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:01:39.710320+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4043",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAF7 were set to 29961569",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:01:29.037105+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRAF7 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:00:28.538072+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4041",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAPPC9 as ready",
"entity_name": "TRAPPC9",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:00:28.524920+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4041",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc9 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC9",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:00:19.891772+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4041",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAPPC9 were changed from MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 13 to Intellectual disability, autosomal recessive 13 (MIM# 613192)",
"entity_name": "TRAPPC9",
"entity_type": "gene"
},
{
"created": "2022-02-23T18:00:07.273160+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAPPC9 were set to ",
"entity_name": "TRAPPC9",
"entity_type": "gene"
},
{
"created": "2022-02-23T17:59:06.871044+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Note multiple intragenic CNVs reported for this gene.; to: Note multiple intragenic CNVs reported for this gene. Cleft lip and brain abnormalities reported.",
"entity_name": "TRAPPC9",
"entity_type": "gene"
},
{
"created": "2022-02-23T17:58:08.676122+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIM37 as ready",
"entity_name": "TRIM37",
"entity_type": "gene"
},
{
"created": "2022-02-23T17:58:08.657001+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim37 has been classified as Green List (High Evidence).",
"entity_name": "TRIM37",
"entity_type": "gene"
},
{
"created": "2022-02-23T17:58:04.122284+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM37 were changed from MULIBREY NANISM to Mulibrey nanism, OMIM #253250",
"entity_name": "TRIM37",
"entity_type": "gene"
},
{
"created": "2022-02-23T17:57:43.478511+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRIM37: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mulibrey nanism, OMIM #253250; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM37",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:44:32.571913+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIP11 as ready",
"entity_name": "TRIP11",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:44:32.560960+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trip11 has been classified as Green List (High Evidence).",
"entity_name": "TRIP11",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:44:28.445742+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIP11 were changed from ACHONDROGENESIS TYPE 1A to Achondrogenesis, type IA, MIM# 200600",
"entity_name": "TRIP11",
"entity_type": "gene"
},
{
"created": "2022-02-23T16:44:15.844397+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.4037",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIP11 were set to ",
"entity_name": "TRIP11",
"entity_type": "gene"
},
{
"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"
}
]
}