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{
"count": 220751,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1589",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1587",
"results": [
{
"created": "2020-09-15T16:25:13.645348+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xrcc2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:24:56.665584+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: XRCC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 27208205, 22232082, 11118202; Phenotypes: Fanconi anemia, complementation group U, MIM# 617247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:24:09.939714+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XRCC2 as ready",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:24:09.930602+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xrcc2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:24:04.067518+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XRCC2 were changed from to Fanconi anemia, complementation group U, MIM# 617247",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:23:36.392165+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XRCC2 were set to ",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:23:09.199756+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: XRCC2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:22:45.550250+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XRCC2 as Amber List (moderate evidence)",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:22:45.541582+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xrcc2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:22:22.493511+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: XRCC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 27208205, 22232082, 11118202; Phenotypes: Fanconi anemia, complementation group U, MIM# 617247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XRCC2",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:14:18.769771+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WIPF1 as ready",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:14:18.755575+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wipf1 has been classified as Green List (High Evidence).",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:14:14.532368+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WIPF1 as Green List (high evidence)",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:14:14.522354+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wipf1 has been classified as Green List (High Evidence).",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:13:45.952657+10:00",
"panel_name": "Bleeding Disorders",
"panel_id": 54,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WIPF1 was added\ngene: WIPF1 was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: WIPF1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WIPF1 were set to 27742395; 11869681; 22231303; 14757742; 9405671\nPhenotypes for gene: WIPF1 were set to Wiskott-Aldrich syndrome 2, MIM#\t614493\nReview for gene: WIPF1 was set to GREEN\nAdded comment: Two unrelated families reported, one with 4 affected individuals. Extensive functional data. \nSources: Expert list",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:12:24.712513+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WIPF1 as ready",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:12:24.701654+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wipf1 has been classified as Green List (High Evidence).",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:12:19.684149+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WIPF1 as Green List (high evidence)",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:12:19.675133+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wipf1 has been classified as Green List (High Evidence).",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T16:11:56.953151+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WIPF1 was added\ngene: WIPF1 was added to Bone Marrow Failure. Sources: Expert list\nMode of inheritance for gene: WIPF1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WIPF1 were set to 27742395; 11869681; 22231303; 14757742; 9405671\nPhenotypes for gene: WIPF1 were set to Wiskott-Aldrich syndrome 2, MIM#\t614493\nReview for gene: WIPF1 was set to GREEN\nAdded comment: Two unrelated families reported, one with 4 affected individuals. Extensive functional data. \nSources: Expert list",
"entity_name": "WIPF1",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:54:13.487901+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSR2 as ready",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:54:13.471443+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:54:10.194842+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSR2 were changed from to Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:53:40.296147+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSR2 were set to ",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:53:10.994506+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSR2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:52:44.764050+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSR2 as Red List (low evidence)",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:52:44.753657+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:52:17.269988+10:00",
"panel_name": "Pierre Robin Sequence",
"panel_id": 160,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSR2: Rating: RED; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:51:29.583117+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSR2 as ready",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:51:29.574072+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:51:16.094306+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSR2 were changed from to Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:50:52.946934+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSR2 were set to ",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:50:34.186618+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSR2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:50:19.314533+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSR2 as Red List (low evidence)",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:50:19.300196+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:50:00.877371+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSR2: Rating: RED; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:49:17.674152+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSR2 as ready",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:49:17.662937+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:49:15.268369+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSR2 were changed from to Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:48:48.160862+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSR2 were set to ",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:48:26.001505+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSR2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:48:00.912164+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSR2 as Red List (low evidence)",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:48:00.901642+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:47:34.421540+10:00",
"panel_name": "Mandibulofacial Acrofacial dysostosis",
"panel_id": 136,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSR2: Rating: RED; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:46:46.424076+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSR2 as ready",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:46:46.411569+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:46:43.552671+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSR2 were changed from to Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:46:20.469094+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSR2 were set to ",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:45:51.661335+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSR2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:45:26.637036+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSR2 as Red List (low evidence)",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:45:26.626931+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:44:58.614388+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSR2: Rating: RED; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:38:55.990640+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.155",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSR2 as ready",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:38:55.981516+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.155",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T15:38:51.884254+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.155",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSR2 were changed from to Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:15:23.889429+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSR2 were set to ",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:15:09.224756+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSR2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:13:41.389709+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TSR2 as Red List (low evidence)",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:13:41.379896+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsr2 has been classified as Red List (Low Evidence).",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:13:12.826437+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSR2: Rating: RED; Mode of pathogenicity: None; Publications: 24942156; Phenotypes: Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TSR2",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:06:18.045189+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: SRP72.",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:06:05.543216+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SRP72 as ready",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:06:05.531732+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: srp72 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:05:57.779487+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SRP72 were changed from to Bone marrow failure syndrome 1, MIM# 614675",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:05:39.002137+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SRP72 were set to ",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:05:21.568061+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SRP72 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:05:05.950894+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SRP72 as Amber List (moderate evidence)",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:05:05.939692+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: srp72 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:04:49.441389+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SRP72: Rating: AMBER; Mode of pathogenicity: None; Publications: 22541560, 31254415; Phenotypes: Bone marrow failure syndrome 1, MIM# 614675; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:04:15.166100+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SRP72 as ready",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:04:15.154398+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: srp72 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:04:12.004671+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SRP72 were changed from to Bone marrow failure syndrome 1, MIM# 614675",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:03:39.675725+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.151",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SRP72 were set to ",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:03:13.362931+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SRP72 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:02:37.030686+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SRP72 as Amber List (moderate evidence)",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:02:37.022002+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: srp72 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:02:14.781116+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag disputed tag was added to gene: SRP72.",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T14:02:05.775422+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SRP72: Rating: AMBER; Mode of pathogenicity: None; Publications: 22541560, 31254415; Phenotypes: Bone marrow failure syndrome 1, MIM# 614675; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SRP72",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:54:23.862370+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SMARCAL1 as ready",
"entity_name": "SMARCAL1",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:54:23.850758+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: smarcal1 has been classified as Green List (High Evidence).",
"entity_name": "SMARCAL1",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:54:20.923730+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SMARCAL1 were changed from to Schimke immunoosseous dysplasia, MIM# 242900",
"entity_name": "SMARCAL1",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:53:52.766718+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SMARCAL1 were set to ",
"entity_name": "SMARCAL1",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:53:30.941787+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SMARCAL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SMARCAL1",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:53:03.200940+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SMARCAL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11799392, 17089404; Phenotypes: Schimke immunoosseous dysplasia, MIM# 242900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SMARCAL1",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:49:31.475982+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLX4 as ready",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:49:31.463180+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slx4 has been classified as Green List (High Evidence).",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:49:28.775923+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLX4 were changed from to Fanconi anemia, complementation group P, MIM# 613951",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:49:05.233928+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLX4 were set to ",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:47:44.809190+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLX4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:47:12.942306+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLX4: Rating: GREEN; Mode of pathogenicity: None; Publications: 21240275, 21240277; Phenotypes: Fanconi anemia, complementation group P, MIM# 613951; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:45:29.475695+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC37A4 as ready",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:45:29.464955+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc37a4 has been classified as Green List (High Evidence).",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:45:26.970375+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC37A4 were changed from to Glycogen storage disease Ib, MIM# 232220",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:44:59.279327+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC37A4 were set to ",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:44:35.214199+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC37A4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:44:11.319633+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC37A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 31788408, 31536830; Phenotypes: Glycogen storage disease Ib, MIM# 232220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:56.942120+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A38 as ready",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:56.930960+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a38 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:44.860008+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A38 were changed from to Anemia, sideroblastic, 2, pyridoxine-refractory, MIM# 205950",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:23.951305+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A38 were set to ",
"entity_name": "SLC25A38",
"entity_type": "gene"
}
]
}