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{
"count": 220790,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1985",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1983",
"results": [
{
"created": "2020-01-15T07:54:52.315394+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR34 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:53:42.944062+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XPNPEP3 were changed from Nephronophthisis-like nephropathy 1, OMIM #613159 to Nephronophthisis-like nephropathy 1, OMIM #613159",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:53:42.367212+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XPNPEP3 as ready",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:53:42.355370+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:52:52.166816+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XPNPEP3 were changed from to Nephronophthisis-like nephropathy 1, OMIM #613159",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:52:16.985617+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XPNPEP3 were set to ",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:51:18.171063+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:50:17.405853+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: C2CD3 as ready",
"entity_name": "C2CD3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:50:17.393795+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: c2cd3 has been classified as Red List (Low Evidence).",
"entity_name": "C2CD3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:50:10.704406+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: C2CD3 were changed from Orofaciodigital syndrome XIV, MIM# 615948 to Orofaciodigital syndrome XIV, MIM# 615948",
"entity_name": "C2CD3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:49:26.833657+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: C2CD3 were changed from to Orofaciodigital syndrome XIV, MIM# 615948",
"entity_name": "C2CD3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:48:46.612775+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: C2CD3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "C2CD3",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:44:40.708061+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL4A1 as ready",
"entity_name": "COL4A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:44:40.696809+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col4a1 has been classified as Green List (High Evidence).",
"entity_name": "COL4A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:44:34.096707+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL4A1 were changed from to Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps, MIM#611773",
"entity_name": "COL4A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:43:39.729991+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: COL4A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "COL4A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:42:41.034070+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CUBN as ready",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:42:41.021223+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cubn has been classified as Red List (Low Evidence).",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:42:24.872254+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FN1 as ready",
"entity_name": "FN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:42:24.860908+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fn1 has been classified as Red List (Low Evidence).",
"entity_name": "FN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:42:03.254579+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LMX1B as ready",
"entity_name": "LMX1B",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:42:03.242876+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lmx1b has been classified as Red List (Low Evidence).",
"entity_name": "LMX1B",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:41:45.686425+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPHS2 as ready",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:41:45.674977+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nphs2 has been classified as Red List (Low Evidence).",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:41:25.616074+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OCRL as ready",
"entity_name": "OCRL",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:41:25.600014+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ocrl has been classified as Red List (Low Evidence).",
"entity_name": "OCRL",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:40:47.677791+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CFHR5 as ready",
"entity_name": "CFHR5",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:40:47.666281+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfhr5 has been classified as Red List (Low Evidence).",
"entity_name": "CFHR5",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:40:21.784274+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CFHR5 were changed from Nephropathy due to CFHR5 deficiency, MIM#614809 to Nephropathy due to CFHR5 deficiency, MIM#614809",
"entity_name": "CFHR5",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:39:39.206206+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CFHR5 were changed from to Nephropathy due to CFHR5 deficiency, MIM#614809",
"entity_name": "CFHR5",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:37:23.888437+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADAMTS13 as ready",
"entity_name": "ADAMTS13",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:37:23.877129+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adamts13 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ADAMTS13",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:37:16.471854+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADAMTS13 were changed from Thrombotic thrombocytopenic purpura, familial, OMIM #274150 to Thrombotic thrombocytopenic purpura, familial, OMIM #274150",
"entity_name": "ADAMTS13",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:36:33.664876+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADAMTS13 were changed from to Thrombotic thrombocytopenic purpura, familial, OMIM #274150",
"entity_name": "ADAMTS13",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:35:55.255050+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADAMTS13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADAMTS13",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:34:41.428029+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: THBD as ready",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:34:41.416361+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: thbd has been classified as Amber List (Moderate Evidence).",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:34:38.157185+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: THBD were changed from {Hemolytic uremic syndrome, atypical, susceptibility to, 6}; OMIM #612926 to {Hemolytic uremic syndrome, atypical, susceptibility to, 6}; OMIM #612926",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:34:03.046393+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: THBD were changed from to {Hemolytic uremic syndrome, atypical, susceptibility to, 6}; OMIM #612926",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:33:26.652647+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: THBD were set to ",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:32:52.481276+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: THBD was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:31:23.496092+11:00",
"panel_name": "Atypical Haemolytic Uraemic Syndrome_MPGN_KidGen_VCGS_RMH",
"panel_id": 211,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: THBD was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "THBD",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:26:31.789733+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JAM2 as ready",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:26:31.778401+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam2 has been classified as Green List (High Evidence).",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:26:23.261991+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: JAM2 as Green List (high evidence)",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:26:23.250543+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam2 has been classified as Green List (High Evidence).",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:26:02.121091+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.790",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: JAM2 was added\ngene: JAM2 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: JAM2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: JAM2 were set to 31851307\nPhenotypes for gene: JAM2 were set to Primary brain calcification\nReview for gene: JAM2 was set to GREEN\nAdded comment: Three unrelated families with bi-allelic variants reported. The clinical phenotypes of the four patients included parkinsonism (3/4), dysarthria (3/4), seizures (1/4), and probable asymptomatic (1/4), with diverse onset ages. \nSources: Literature",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:23:41.311064+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JAM2 as ready",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:23:41.299830+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam2 has been classified as Green List (High Evidence).",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:23:36.628384+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: JAM2 as Green List (high evidence)",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:23:36.617009+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam2 has been classified as Green List (High Evidence).",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:23:00.784833+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: JAM2 was added\ngene: JAM2 was added to Brain calcification_VCGS. Sources: Literature\nMode of inheritance for gene: JAM2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: JAM2 were set to 31851307\nPhenotypes for gene: JAM2 were set to Primary brain calcification\nAdded comment: Three unrelated families with bi-allelic variants reported. The clinical phenotypes of the four patients included parkinsonism (3/4), dysarthria (3/4), seizures (1/4), and probable asymptomatic (1/4), with diverse onset ages. \nSources: Literature",
"entity_name": "JAM2",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:16:49.673194+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAM160B1 as ready",
"entity_name": "FAM160B1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:16:49.661430+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam160b1 has been classified as Red List (Low Evidence).",
"entity_name": "FAM160B1",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:40:35.578205+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLCNKB as ready",
"entity_name": "CLCNKB",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:40:35.566478+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clcnkb has been classified as Green List (High Evidence).",
"entity_name": "CLCNKB",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:38:45.772712+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLCNKB were changed from Bartter syndrome, type 3, MIM#607364; Bartter syndrome, type 4b, digenic, MIM#613090 to Bartter syndrome, type 3, MIM#607364; Bartter syndrome, type 4b, digenic, MIM#613090",
"entity_name": "CLCNKB",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:38:16.399897+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1585",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLCNKB were changed from to Bartter syndrome, type 3, MIM#607364; Bartter syndrome, type 4b, digenic, MIM#613090",
"entity_name": "CLCNKB",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:37:32.212052+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AP1B1 as ready",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:37:32.200402+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1b1 has been classified as Green List (High Evidence).",
"entity_name": "AP1B1",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:37:04.119253+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLCNKA as ready",
"entity_name": "CLCNKA",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:37:04.106581+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clcnka has been classified as Green List (High Evidence).",
"entity_name": "CLCNKA",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:36:50.707717+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLCNKB were set to ",
"entity_name": "CLCNKB",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:36:20.718742+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1583",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CLCNKB was changed from Unknown to Other",
"entity_name": "CLCNKB",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:35:29.273681+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLCNKA were changed from to Bartter syndrome, type 4b, digenic, MIM#613090",
"entity_name": "CLCNKA",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:35:17.993225+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COASY as ready",
"entity_name": "COASY",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:35:17.979899+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: coasy has been classified as Green List (High Evidence).",
"entity_name": "COASY",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:35:07.169478+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLCNKA were set to ",
"entity_name": "CLCNKA",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:34:45.268398+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CLCNKA was changed from Other to Other",
"entity_name": "CLCNKA",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:34:21.974578+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CLCNKA was changed from Unknown to Other",
"entity_name": "CLCNKA",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:32:59.848153+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1580",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COASY were changed from Neurodegeneration with brain iron accumulation 6 615643; Pontocerebellar hypoplasia, type 12 618266 to Neurodegeneration with brain iron accumulation 6 615643; Pontocerebellar hypoplasia, type 12 618266",
"entity_name": "COASY",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:32:33.303048+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1580",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COG6 were changed from Congenital disorder of glycosylation, type Iil, MIM#614576 to Congenital disorder of glycosylation, type Iil, MIM#614576",
"entity_name": "COG6",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:32:10.299042+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COG6 as ready",
"entity_name": "COG6",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:32:09.584884+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cog6 has been classified as Green List (High Evidence).",
"entity_name": "COG6",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:32:04.854739+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COASY were changed from to Neurodegeneration with brain iron accumulation 6 615643; Pontocerebellar hypoplasia, type 12 618266",
"entity_name": "COASY",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:31:37.609036+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COASY were set to 24360804; 30089828",
"entity_name": "COASY",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:31:11.547597+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COG6 were changed from to Congenital disorder of glycosylation, type Iil, MIM#614576",
"entity_name": "COG6",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:30:48.738050+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1578",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COASY were set to ",
"entity_name": "COASY",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:30:20.933492+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1578",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: COASY was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COASY",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:29:25.163941+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1577",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: COG6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COG6",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:29:18.236871+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COQ9 as ready",
"entity_name": "COQ9",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:29:18.223863+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: coq9 has been classified as Green List (High Evidence).",
"entity_name": "COQ9",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:28:26.270038+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COQ9 were changed from to Coenzyme Q10 deficiency, primary, 5, MIM#614654",
"entity_name": "COQ9",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:27:55.678868+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: COQ9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COQ9",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:26:33.662603+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ETFA as ready",
"entity_name": "ETFA",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:26:33.650990+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: etfa has been classified as Green List (High Evidence).",
"entity_name": "ETFA",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:25:55.803885+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ETFDH as ready",
"entity_name": "ETFDH",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:25:55.788672+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: etfdh has been classified as Green List (High Evidence).",
"entity_name": "ETFDH",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:25:15.054431+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FARS2 as ready",
"entity_name": "FARS2",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:25:15.036561+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fars2 has been classified as Green List (High Evidence).",
"entity_name": "FARS2",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:24:45.505768+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MAP1B as ready",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:24:45.494627+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: map1b has been classified as Green List (High Evidence).",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:24:17.196715+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KLF7 as ready",
"entity_name": "KLF7",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:24:17.184956+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: klf7 has been classified as Green List (High Evidence).",
"entity_name": "KLF7",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:23:54.659748+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MAP1B were changed from to Intellectual disability; seizures; PVNH; dysmorphic features",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:23:26.665334+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MAP1B were set to ",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:22:53.749122+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MAP1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:21:56.691656+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1571",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED17 as ready",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:21:56.680364+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1571",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med17 has been classified as Green List (High Evidence).",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2020-01-14T21:21:42.689240+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1571",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MED17 were changed from to Microcephaly, postnatal progressive, with seizures and brain atrophy, MIM#613668",
"entity_name": "MED17",
"entity_type": "gene"
}
]
}