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{
"count": 220212,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=886",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=884",
"results": [
{
"created": "2022-04-11T16:22:15.797255+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12848",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CD40 as ready",
"entity_name": "CD40",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:22:15.784030+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12848",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cd40 has been classified as Green List (High Evidence).",
"entity_name": "CD40",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:22:00.713958+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12848",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CD40 were changed from to Immunodeficiency with hyper-IgM, type 3, MIM# 606843",
"entity_name": "CD40",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:21:54.996905+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12847",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CD40 were set to ",
"entity_name": "CD40",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:21:50.479480+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12847",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CD40 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CD40",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:21:31.225028+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12846",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CD40: Rating: GREEN; Mode of pathogenicity: None; Publications: 11675497, 12915844; Phenotypes: Immunodeficiency with hyper-IgM, type 3, MIM# 606843; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "CD40",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:21:11.945739+10:00",
"panel_name": "Oligodontia",
"panel_id": 148,
"panel_version": "0.13",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: PAX9: Rating: GREEN; Mode of pathogenicity: None; Publications: 10615120, 16479262; Phenotypes: Tooth agenesis, selective, 3 - MIM#604625; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PAX9",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:20:36.060258+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12846",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CD36 as ready",
"entity_name": "CD36",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:20:36.048527+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12846",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cd36 has been classified as Green List (High Evidence).",
"entity_name": "CD36",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:20:29.661725+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12846",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CD36 were changed from to Platelet glycoprotein IV deficiency MIM#608404; {Malaria, cerebral, reduced risk of} MIM#611162; {Malaria, cerebral, susceptibility to} MIM#611162",
"entity_name": "CD36",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:20:11.282850+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12845",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CD36 were set to ",
"entity_name": "CD36",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:20:06.819901+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12845",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CD36 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CD36",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:19:49.758089+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12844",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CD36: Rating: GREEN; Mode of pathogenicity: None; Publications: 7686693, 11950861, 10890433, 24960640, 10890433; Phenotypes: Platelet glycoprotein IV deficiency MIM#608404, {Malaria, cerebral, reduced risk of} MIM#611162, {Malaria, cerebral, susceptibility to} MIM#611162; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "CD36",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:16:11.297557+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12844",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Deleted their review",
"entity_name": "CD36",
"entity_type": "gene"
},
{
"created": "2022-04-11T16:16:03.912119+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12844",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CD36: Rating: GREEN; Mode of pathogenicity: None; Publications: 7533783, 11950861, 10890433, 12506336; Phenotypes: {Malaria, cerebral, reduced risk of} MIM#611162, {Malaria, cerebral, susceptibility to} MIM#611162, Platelet glycoprotein IV deficiency MIM#608404; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "CD36",
"entity_type": "gene"
},
{
"created": "2022-04-11T15:56:37.444704+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12844",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CD209 as ready",
"entity_name": "CD209",
"entity_type": "gene"
},
{
"created": "2022-04-11T15:56:37.434205+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12844",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cd209 has been classified as Red List (Low Evidence).",
"entity_name": "CD209",
"entity_type": "gene"
},
{
"created": "2022-04-11T15:56:31.355222+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12844",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CD209 were changed from to {Dengue fever, protection against} MIM#614371; {HIV type 1, susceptibility to} MIM#609423; {Mycobacterium tuberculosis, susceptibility to} MIM#607948",
"entity_name": "CD209",
"entity_type": "gene"
},
{
"created": "2022-04-11T15:56:19.539802+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12844",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Classified gene: CD209 as Red List (low evidence)",
"entity_name": "CD209",
"entity_type": "gene"
},
{
"created": "2022-04-11T15:56:19.527546+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12844",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cd209 has been classified as Red List (Low Evidence).",
"entity_name": "CD209",
"entity_type": "gene"
},
{
"created": "2022-04-11T15:56:02.080345+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12843",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CD209: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Dengue fever, protection against} MIM#614371, {HIV type 1, susceptibility to} MIM#609423, {Mycobacterium tuberculosis, susceptibility to} MIM#607948; Mode of inheritance: None; Current diagnostic: yes",
"entity_name": "CD209",
"entity_type": "gene"
},
{
"created": "2022-04-11T14:14:23.318265+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12843",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CD151 as ready",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2022-04-11T14:14:23.298760+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12843",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: cd151 has been classified as Green List (High Evidence).",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2022-04-11T14:14:07.272106+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12843",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CD151 were changed from to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2022-04-11T14:14:00.655741+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12842",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CD151 were set to ",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2022-04-11T14:13:56.184085+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12842",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CD151 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2022-04-11T14:13:39.809755+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12841",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CD151: Rating: GREEN; Mode of pathogenicity: None; Publications: 15265795, 29138120; Phenotypes: Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:32:33.787857+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12841",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CCR5 as ready",
"entity_name": "CCR5",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:32:33.778086+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12841",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: ccr5 has been classified as Green List (High Evidence).",
"entity_name": "CCR5",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:32:07.176239+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12841",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CCR5 were changed from to {Hepatitis C virus, resistance to} 609532; {HIV infection, susceptibility/resistance to}; {West nile virus, susceptibility to}MIM# 610379",
"entity_name": "CCR5",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:31:53.887867+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12840",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Mode of inheritance for gene: CCR5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CCR5",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:31:34.436445+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12839",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CCR5: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: {Hepatitis C virus, resistance to} 609532, {HIV infection, susceptibility/resistance to}, {West nile virus, susceptibility to}MIM# 610379; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "CCR5",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:30:53.420292+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12839",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Phenotypes for gene: CCR2 were changed from to {HIV infection, susceptibility/resistance to}",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:30:42.978884+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12839",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Publications for gene: CCR2 were set to ",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:30:21.330072+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12838",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "edited their review of gene: CCR2: Changed publications: 34516427, 17504215, 15167933, 17604544",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T12:25:02.468749+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12838",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "changed review comment from: Currently no mendelian gene-disease association; to: Vall64Ile has been associated with reduction in the progression to AIDS. Mutant results in normal expression levels of the CCR2 receptor and has no effect on the incidence of HIV infection. However, in contrast to normal CCR2 peptides, the mutant protein preferentially dimerizes with the CXCR4 polypeptide, isolating it in the endoplasmic reticulum. It is also thought that the inhibitory effect is dependent on the stages of HIV-1 infection and interactions with other genetic variants.",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:47:52.164851+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12838",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "edited their review of gene: CCR2: Changed phenotypes: {HIV infection, susceptibility/resistance to}",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:39:48.851813+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12838",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Classified gene: CCR2 as Red List (low evidence)",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:39:48.840616+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12838",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: ccr2 has been classified as Red List (Low Evidence).",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:39:25.545404+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12837",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Classified gene: CCR2 as Red List (low evidence)",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:39:25.533373+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12837",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: ccr2 has been classified as Red List (Low Evidence).",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:39:23.397091+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12836",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Marked gene: CCR2 as ready",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:39:23.386074+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12836",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "Gene: ccr2 has been classified as Green List (High Evidence).",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:35:51.504586+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12836",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: CCR2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None; Current diagnostic: yes",
"entity_name": "CCR2",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:08:13.685501+10:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.245",
"user_name": "Abhijit Kulkarni",
"item_type": "entity",
"text": "reviewed gene: GBA: Rating: GREEN; Mode of pathogenicity: None; Publications: 33897756, 33082562, 29854527; Phenotypes: GAUCHER DISEASE, MIM: 608013; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-04-11T11:01:29.867266+10:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.245",
"user_name": "Abhijit Kulkarni",
"item_type": "entity",
"text": "reviewed gene: GALNS: Rating: GREEN; Mode of pathogenicity: None; Publications: 33082562, 23137060; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GALNS",
"entity_type": "gene"
},
{
"created": "2022-04-11T10:13:12.663303+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1553",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A12",
"entity_type": "gene"
},
{
"created": "2022-04-11T10:12:34.059813+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1552",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A12: Rating: GREEN; Mode of pathogenicity: None; Publications: 19641205, 24515575, 35008954, 32700846, 31766059, 31514314; Phenotypes: Developmental and epileptic encephalopathy 39, MIM# 612949; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A12",
"entity_type": "gene"
},
{
"created": "2022-04-11T10:11:17.960178+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12836",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A12 as ready",
"entity_name": "SLC25A12",
"entity_type": "gene"
},
{
"created": "2022-04-11T10:11:17.948050+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12836",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a12 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A12",
"entity_type": "gene"
},
{
"created": "2022-04-11T10:11:08.859406+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12836",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A12 were changed from to Developmental and epileptic encephalopathy 39, MIM# 612949",
"entity_name": "SLC25A12",
"entity_type": "gene"
},
{
"created": "2022-04-11T10:10:48.061812+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A12 were set to ",
"entity_name": "SLC25A12",
"entity_type": "gene"
},
{
"created": "2022-04-11T10:10:26.171945+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A12",
"entity_type": "gene"
},
{
"created": "2022-04-11T10:10:06.146730+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A12: Rating: GREEN; Mode of pathogenicity: None; Publications: 19641205, 24515575, 35008954, 32700846, 31766059, 31514314; Phenotypes: Developmental and epileptic encephalopathy 39, MIM# 612949; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A12",
"entity_type": "gene"
},
{
"created": "2022-04-11T09:59:01.259071+10:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.245",
"user_name": "Abhijit Kulkarni",
"item_type": "entity",
"text": "reviewed gene: FOXC2: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301630, 2525212, 21918810, 25712632; Phenotypes: Lymphedema-distichiasis syndrome, MIM:153400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FOXC2",
"entity_type": "gene"
},
{
"created": "2022-04-11T09:00:15.836595+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A13 as ready",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2022-04-11T09:00:15.825198+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a13 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2022-04-11T09:00:00.221570+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A13 were changed from to Citrullinemia, type II, neonatal-onset, MIM# 605814; Citrullinemia, adult-onset type II, MIM# 603471",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:59:38.771684+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12832",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A13 were set to ",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:59:14.972183+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:58:52.221936+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A13: Rating: GREEN; Mode of pathogenicity: None; Publications: 21424115, 11343052; Phenotypes: Citrullinemia, type II, neonatal-onset, MIM# 605814, Citrullinemia, adult-onset type II, MIM# 603471; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:56:16.464670+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A15 as ready",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:56:16.453144+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a15 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:56:06.486188+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A15 were changed from to Hyperornithinaemia-hyperammonaemia-homocitrullinaemia syndrome , MIM#238970",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:55:38.523122+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A15 were set to ",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:55:14.039658+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2022-04-11T08:54:15.599006+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A15: Rating: GREEN; Mode of pathogenicity: None; Publications: 10369256, 19242930]; Phenotypes: Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome , MIM#238970; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:48:47.493399+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A19 as ready",
"entity_name": "SLC25A19",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:48:47.483021+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a19 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A19",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:47:20.383646+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A19 were changed from to Microcephaly, Amish type, MIM#607196; Thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type), MIM#613710",
"entity_name": "SLC25A19",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:46:59.308461+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12826",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A19 were set to ",
"entity_name": "SLC25A19",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:46:20.305208+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A19",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:45:59.382529+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A19: Rating: GREEN; Mode of pathogenicity: None; Publications: 31506564, 31295743, 12185364, 19798730; Phenotypes: Microcephaly, Amish type, MIM#607196, Thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type), MIM#613710; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A19",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:44:55.648133+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1552",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A22 as ready",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:44:55.634833+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1552",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a22 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:44:32.656805+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1552",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A22 were changed from to Developmental and epileptic encephalopathy 3, MIM# 609304",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:44:00.333483+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1551",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A22 were set to ",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:43:57.641069+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A22 as ready",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:43:57.625954+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a22 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:43:49.009143+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A22 were changed from to Developmental and epileptic encephalopathy 3, MIM# 609304",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:43:29.440493+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12823",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A22 were set to ",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:43:29.084451+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1550",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A22 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:42:50.909916+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1549",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A22: Rating: GREEN; Mode of pathogenicity: None; Publications: 15592994, 19780765, 24596948, 33821742, 33342683, 31285529; Phenotypes: Developmental and epileptic encephalopathy 3, MIM# 609304; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:42:40.207061+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12822",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A22 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:41:53.457529+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A22: Rating: GREEN; Mode of pathogenicity: None; Publications: 15592994, 19780765, 24596948, 33821742, 33342683, 31285529; Phenotypes: Developmental and epileptic encephalopathy 3, MIM# 609304; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A22",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:35:24.344312+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRPM1 as ready",
"entity_name": "TRPM1",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:35:24.309763+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpm1 has been classified as Green List (High Evidence).",
"entity_name": "TRPM1",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:35:15.753512+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRPM1 were changed from to Night blindness, congenital stationary (complete), 1C, autosomal recessive, MIM# 613216",
"entity_name": "TRPM1",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:34:54.739110+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12820",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRPM1 were set to ",
"entity_name": "TRPM1",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:34:35.837108+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRPM1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRPM1",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:34:17.111627+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRPM1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19878917, 19896113, 19896109; Phenotypes: Night blindness, congenital stationary (complete), 1C, autosomal recessive, MIM# 613216; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRPM1",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:32:49.565437+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRPC6 as ready",
"entity_name": "TRPC6",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:32:49.553738+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpc6 has been classified as Green List (High Evidence).",
"entity_name": "TRPC6",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:32:47.347495+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRPC6 were changed from to Glomerulosclerosis, focal segmental, 2, MIM# 603965",
"entity_name": "TRPC6",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:32:25.333226+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRPC6 were set to 15879175; 15924139; 34387384; 33918778; 32509715",
"entity_name": "TRPC6",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:32:04.070790+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRPC6 were set to ",
"entity_name": "TRPC6",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:31:49.882051+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRPC6 as ready",
"entity_name": "TRPC6",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:31:49.869401+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpc6 has been classified as Green List (High Evidence).",
"entity_name": "TRPC6",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:31:26.464271+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRPC6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRPC6",
"entity_type": "gene"
},
{
"created": "2022-04-09T17:30:54.406677+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRPC6: Rating: GREEN; Mode of pathogenicity: None; Publications: 15879175, 15924139, 34387384, 33918778, 32509715; Phenotypes: Glomerulosclerosis, focal segmental, 2, MIM# 603965; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRPC6",
"entity_type": "gene"
}
]
}