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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=246",
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"results": [
{
"created": "2025-04-30T14:15:04.676153+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLN8 as ready",
"entity_name": "CLN8",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:15:04.666758+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cln8 has been classified as Green List (High Evidence).",
"entity_name": "CLN8",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:15:02.245524+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLN8 were changed from Ceroid lipofuscinosis, neuronal, 8, 600143 (3) to Ceroid lipofuscinosis, neuronal, 8, MIM# 600143",
"entity_name": "CLN8",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:14:32.415448+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLN6 as ready",
"entity_name": "CLN6",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:14:32.405966+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cln6 has been classified as Green List (High Evidence).",
"entity_name": "CLN6",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:14:30.640194+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLN6 were changed from Ceroid lipofuscinosis, neuronal 6, 601780 (3) to Ceroid lipofuscinosis, neuronal 6, MIM#601780",
"entity_name": "CLN6",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:14:21.102843+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLN6 were set to ",
"entity_name": "CLN6",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:14:05.586479+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLN5 as ready",
"entity_name": "CLN5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:14:05.580373+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cln5 has been classified as Green List (High Evidence).",
"entity_name": "CLN5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:14:00.261345+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLN5 were changed from Ceroid lipofuscinosis, neuronal, 5, 256731 (3) to Ceroid lipofuscinosis, neuronal, 5, MIM# 256731; MONDO:0009745",
"entity_name": "CLN5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:13:42.388906+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLCN7 as ready",
"entity_name": "CLCN7",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:13:42.381186+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clcn7 has been classified as Green List (High Evidence).",
"entity_name": "CLCN7",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:13:39.125008+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLCN7 were changed from Osteopetrosis, autosomal recessive 4, 611490 (3) to Osteopetrosis, autosomal recessive 4, MIM#611490",
"entity_name": "CLCN7",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:13:28.931956+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLCN7 were set to ",
"entity_name": "CLCN7",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:13:12.798802+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLCN5 as ready",
"entity_name": "CLCN5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:13:12.789376+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clcn5 has been classified as Green List (High Evidence).",
"entity_name": "CLCN5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:13:10.337186+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLCN5 were changed from Dent disease, 300009 (3) to Dent disease, MIM#300009",
"entity_name": "CLCN5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:12:50.814363+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CKAP2L as ready",
"entity_name": "CKAP2L",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:12:50.807497+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ckap2l has been classified as Green List (High Evidence).",
"entity_name": "CKAP2L",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:12:48.025190+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CKAP2L were changed from Filippi syndrome, 272440 (3) to Filippi syndrome MIM#272440",
"entity_name": "CKAP2L",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:12:38.248185+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CKAP2L were set to ",
"entity_name": "CKAP2L",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:12:19.346323+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CIITA as ready",
"entity_name": "CIITA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:12:19.339970+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ciita has been classified as Green List (High Evidence).",
"entity_name": "CIITA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:12:16.858544+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CIITA were changed from Bare lymphocyte syndrome, type II, complementation group A, 209920 (3) to MHC class II deficiency 1 MIM#209920",
"entity_name": "CIITA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:11:54.444626+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CIITA were set to ",
"entity_name": "CIITA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:11:09.951367+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHRNG as ready",
"entity_name": "CHRNG",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:11:09.943922+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chrng has been classified as Green List (High Evidence).",
"entity_name": "CHRNG",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:11:08.047996+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CHRNG were changed from Escobar syndrome, 265000 (3) to Escobar syndrome (MIM# 265000); Multiple pterygium syndrome, lethal type, (MIM# 253290)",
"entity_name": "CHRNG",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:10:47.251698+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CHRNG were set to ",
"entity_name": "CHRNG",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:10:28.934491+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHRNE as ready",
"entity_name": "CHRNE",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:10:28.924138+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chrne has been classified as Green List (High Evidence).",
"entity_name": "CHRNE",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:10:26.578373+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CHRNE were changed from Myasthenic syndrome, congenital, 4A, slow-channel, 605809 (3) to Myasthenic syndrome, congenital, 4A, slow-channel MIM#605809; Myasthenic syndrome, congenital, 4B, fast-channel MIM#616324; Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency MIM#608931",
"entity_name": "CHRNE",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:10:16.131068+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CHRNE were set to ",
"entity_name": "CHRNE",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:09:43.942087+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHAT as ready",
"entity_name": "CHAT",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:09:43.935285+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chat has been classified as Green List (High Evidence).",
"entity_name": "CHAT",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:09:31.907140+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CHAT were changed from Myasthenic syndrome, congenital, 6, presynaptic, 254210 (3) to Myasthenic syndrome, congenital, 6, presynaptic MIM#254210",
"entity_name": "CHAT",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:08:38.933770+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CHAT were set to ",
"entity_name": "CHAT",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:08:11.481795+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CFTR as ready",
"entity_name": "CFTR",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:08:11.470781+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cftr has been classified as Green List (High Evidence).",
"entity_name": "CFTR",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:08:09.337035+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CFTR were changed from Cystic fibrosis, 219700 (3) to Cystic fibrosis, MIM#219700; MONDO:0009061",
"entity_name": "CFTR",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:08:00.573790+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CFTR were set to ",
"entity_name": "CFTR",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:07:41.696139+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CEP41 as ready",
"entity_name": "CEP41",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:07:41.689637+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep41 has been classified as Green List (High Evidence).",
"entity_name": "CEP41",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:07:39.462963+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CEP41 were changed from Joubert syndrome 15, 614464 (3) to Joubert syndrome 15, MIM# 614464",
"entity_name": "CEP41",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:07:29.413813+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CEP41 were set to ",
"entity_name": "CEP41",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:07:13.091064+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CEP290 as ready",
"entity_name": "CEP290",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:07:13.083204+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep290 has been classified as Green List (High Evidence).",
"entity_name": "CEP290",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:07:10.496166+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CEP290 were changed from Joubert syndrome 5, 610188 (3) to CEP290-related ciliopathy MONDO:0100451; Bardet-Biedl syndrome 14, MIM# 615991; Joubert syndrome 5 610188; Leber congenital amaurosis 10, MIM# 611755; Meckel syndrome 4, MIM# 611134; Senior-Loken syndrome 6, MIM# 610189",
"entity_name": "CEP290",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:07:00.852754+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CEP290 were set to ",
"entity_name": "CEP290",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:06:33.811777+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CEP152 as ready",
"entity_name": "CEP152",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:06:33.805526+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep152 has been classified as Green List (High Evidence).",
"entity_name": "CEP152",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:06:31.185498+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CEP152 were changed from Seckel syndrome 5, 613823 (3) to Microcephaly 9, primary, autosomal recessive, MIM# 614852; MONDO:0013923; Seckel syndrome 5, MIM# 613823; MONDO:0013443",
"entity_name": "CEP152",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:06:22.459285+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CEP152 were set to ",
"entity_name": "CEP152",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:06:03.210942+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CENPJ as ready",
"entity_name": "CENPJ",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:06:03.200480+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cenpj has been classified as Green List (High Evidence).",
"entity_name": "CENPJ",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:06:00.602512+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CENPJ were changed from Microcephaly 6, primary, autosomal recessive, 608393 (3) to Microcephaly 6, primary MIM#608393; Seckel syndrome 4 MIM#613676",
"entity_name": "CENPJ",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:05:51.144644+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CENPJ were set to ",
"entity_name": "CENPJ",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:05:26.636918+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDH23 as ready",
"entity_name": "CDH23",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:05:26.630807+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdh23 has been classified as Green List (High Evidence).",
"entity_name": "CDH23",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:05:22.035455+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CDH23 were changed from Usher syndrome, type 1D, 601067 (3) to Usher syndrome, type 1D (MIM#601067)",
"entity_name": "CDH23",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:05:11.419752+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CDH23 were set to ",
"entity_name": "CDH23",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:04:55.469722+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CD40LG as ready",
"entity_name": "CD40LG",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:04:55.462498+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd40lg has been classified as Green List (High Evidence).",
"entity_name": "CD40LG",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:04:53.255260+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CD40LG were changed from Immunodeficiency, X-linked, with hyper-IgM, 308230 (3) to Immunodeficiency, X-linked, with hyper-IgM MIM# 308230",
"entity_name": "CD40LG",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:04:44.021343+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.166",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CD40LG were set to ",
"entity_name": "CD40LG",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:56:31.525249+10:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.56",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Marked gene: IFT57 as ready",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:56:31.518836+10:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.56",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:56:05.969038+10:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.56",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: IFT57 as Amber List (moderate evidence)",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:56:05.958517+10:00",
"panel_name": "Cone-rod Dystrophy",
"panel_id": 3147,
"panel_version": "0.56",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:54:49.492422+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.283",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: IFT57 as Amber List (moderate evidence)",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:54:49.483046+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.283",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:54:15.936594+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "1.68",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: IFT57 as Amber List (moderate evidence)",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:54:15.930340+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "1.68",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:54:08.398124+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "1.67",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Marked gene: IFT57 as ready",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:54:08.386172+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "1.67",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Red List (Low Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:53:46.411325+10:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "1.12",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Marked gene: IFT57 as ready",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:53:46.404872+10:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "1.12",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:53:42.790077+10:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "1.12",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: IFT57 as Amber List (moderate evidence)",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:53:42.784093+10:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "1.12",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:53:10.709453+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2519",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Phenotypes for gene: IFT57 were changed from Orofaciodigital syndrome XVIII, MIM# 617927; Bardet-Bield syndrome; ciliopathy - MONDO:0005308 to Orofaciodigital syndrome XVIII, MIM# 617927; Bardet-Bield syndrome; ciliopathy - MONDO:0005308",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:53:06.857643+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2518",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Phenotypes for gene: IFT57 were changed from Orofaciodigital syndrome XVIII, MIM# 617927 to Orofaciodigital syndrome XVIII, MIM# 617927; Bardet-Bield syndrome; ciliopathy - MONDO:0005308",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:52:50.109385+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2517",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: IFT57 as Amber List (moderate evidence)",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:52:50.102451+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2517",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:51:36.992496+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.120",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: UGGT1 as Green List (high evidence)",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:51:36.980212+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.120",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: uggt1 has been classified as Green List (High Evidence).",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:51:28.716151+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.119",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Marked gene: UGGT1 as ready",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:51:28.708655+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.119",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: uggt1 has been classified as Red List (Low Evidence).",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:50:50.478749+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.146",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: UGGT1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID:40267907; Phenotypes: Congenital disorder of glycosylation - MONDO:0015286, UGGT1-CDG; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:50:13.596350+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.146",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: UGGT1 as Green List (high evidence)",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:50:13.585677+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.146",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: uggt1 has been classified as Green List (High Evidence).",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:49:24.860870+10:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.85",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: UGGT1 as Amber List (moderate evidence)",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:49:24.855040+10:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.85",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: uggt1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:49:12.123166+10:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.85",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Marked gene: UGGT1 as ready",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:49:12.115103+10:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.85",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: uggt1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:49:11.213881+10:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.85",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: UGGT1 as Amber List (moderate evidence)",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:49:11.202645+10:00",
"panel_name": "Renal Macrocystic Disease",
"panel_id": 194,
"panel_version": "0.85",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: uggt1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:48:18.921206+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.305",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Classified gene: UGGT1 as Green List (high evidence)",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:48:18.911826+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.305",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: uggt1 has been classified as Green List (High Evidence).",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:48:12.133750+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.304",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Marked gene: UGGT1 as ready",
"entity_name": "UGGT1",
"entity_type": "gene"
},
{
"created": "2025-04-30T11:48:12.121823+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "1.304",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "Gene: uggt1 has been classified as Red List (Low Evidence).",
"entity_name": "UGGT1",
"entity_type": "gene"
}
]
}