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{
"count": 220377,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2061",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2059",
"results": [
{
"created": "2019-12-08T07:04:25.192695+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EXT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EXT2",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:01:48.543533+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NECAP1 as ready",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:01:48.536040+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: necap1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:01:44.368861+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NECAP1 as Amber List (moderate evidence)",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:01:44.358129+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: necap1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T07:01:13.813358+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NECAP1 was added\ngene: NECAP1 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: NECAP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NECAP1 were set to 24399846; 30626896; 30525121\nPhenotypes for gene: NECAP1 were set to Epileptic encephalopathy, early infantile, 21, MIM#615833\nReview for gene: NECAP1 was set to AMBER\nAdded comment: Three families, but two of these have the same founder variant; no functional data. \nSources: Literature",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:58:46.057689+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.862",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NECAP1 as ready",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:58:46.050377+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.862",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: necap1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:58:41.090996+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.862",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NECAP1 were changed from to Epileptic encephalopathy, early infantile, 21, MIM#615833",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:58:29.412838+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.861",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NECAP1 were set to ",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:58:20.297114+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.860",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NECAP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:58:13.102059+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.859",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NECAP1 as Amber List (moderate evidence)",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:58:13.098788+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.859",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Three families, but two of these have the same founder variant; no functional data.",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:58:13.080561+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.859",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: necap1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-08T06:56:44.943922+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.858",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NECAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24399846, 30626896, 30525121; Phenotypes: Epileptic encephalopathy, early infantile, 21, MIM#615833; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NECAP1",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:35:28.443835+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.858",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFV2 as ready",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:35:28.436951+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.858",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufv2 has been classified as Green List (High Evidence).",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:35:23.982306+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.858",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFV2 were changed from to Mitochondrial complex I deficiency, nuclear type 7, MIM#618229",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:35:12.632068+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.857",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFV2 were set to ",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:35:04.814667+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.856",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFV2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:34:50.710290+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.855",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFV2: Rating: GREEN; Mode of pathogenicity: None; Publications: 12754703, 26008862, 29554876; Phenotypes: Mitochondrial complex I deficiency, nuclear type 7, MIM#618229; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFV2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:30:21.781416+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.855",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS6 as ready",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:30:21.774486+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.855",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs6 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:30:16.743628+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.855",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS6 were changed from to Mitochondrial complex I deficiency, nuclear type 9, MIM#618232",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:30:05.196940+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.854",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS6 were set to ",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:29:52.335052+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.853",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFS6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:29:38.756253+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.852",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFS6: Rating: GREEN; Mode of pathogenicity: None; Publications: 15372108, 19259137, 30948790, 22474353; Phenotypes: Mitochondrial complex I deficiency, nuclear type 9, MIM#618232; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:23:45.626218+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.852",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS3 as ready",
"entity_name": "NDUFS3",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:23:45.617968+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.852",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs3 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS3",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:23:40.590801+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.852",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS3 were changed from to Mitochondrial complex I deficiency, nuclear type 8, MIM#618230",
"entity_name": "NDUFS3",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:23:27.923188+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.851",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS3 were set to ",
"entity_name": "NDUFS3",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:23:15.708804+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.850",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFS3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS3",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:22:49.324987+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFS3: Rating: GREEN; Mode of pathogenicity: None; Publications: 14729820, 22499348, 30140060; Phenotypes: Mitochondrial complex I deficiency, nuclear type 8, MIM#618230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS3",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:19:01.850049+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS2 as ready",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:19:01.842347+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs2 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:18:39.154547+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.849",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS2 were changed from to Mitochondrial complex I deficiency, nuclear type 6, MIM#618228",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:18:26.683491+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.848",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS2 were set to ",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:18:16.545719+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.847",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2019-12-07T20:18:03.214015+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.846",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFS2: Rating: GREEN; Mode of pathogenicity: None; Publications: 11220739, 31411514, 29272804; Phenotypes: Mitochondrial complex I deficiency, nuclear type 6, MIM#618228; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:43:34.702287+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFB9 as ready",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:43:34.695345+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufb9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:43:25.945237+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFB9 were changed from to Mitochondrial complex I deficiency, nuclear type 24, MIM#618245",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:43:02.812472+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFB9 were set to ",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:42:54.560629+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFB9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:42:40.864304+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFB9 as Amber List (moderate evidence)",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:42:40.855493+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufb9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:42:21.621549+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFB9: Rating: AMBER; Mode of pathogenicity: None; Publications: 22200994; Phenotypes: Mitochondrial complex I deficiency, nuclear type 24, MIM#618245; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:40:50.230338+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFB9 were changed from to Mitochondrial complex I deficiency, nuclear type 24, MIM#618245",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:40:47.695129+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFB9 as ready",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:40:47.686772+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufb9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:40:33.420275+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFB9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:40:17.064685+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFB9 as Amber List (moderate evidence)",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:40:16.758849+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufb9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:39:49.836884+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFB9: Rating: AMBER; Mode of pathogenicity: None; Publications: 22200994; Phenotypes: Mitochondrial complex I deficiency, nuclear type 24, MIM#618245; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:38:52.647926+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.846",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFB9 were changed from to Mitochondrial complex I deficiency, nuclear type 24, MIM#618245",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:38:40.662277+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.845",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFB9 were set to ",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:38:30.310785+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.844",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFB9 as Amber List (moderate evidence)",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:38:30.303854+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.844",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufb9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:38:16.587086+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.843",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFB9: Rating: AMBER; Mode of pathogenicity: None; Publications: 22200994; Phenotypes: Mitochondrial complex I deficiency, nuclear type 24, MIM#618245; Mode of inheritance: None",
"entity_name": "NDUFB9",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:35:24.661442+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.843",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFB3 as ready",
"entity_name": "NDUFB3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:35:24.654373+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.843",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufb3 has been classified as Green List (High Evidence).",
"entity_name": "NDUFB3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:35:12.939726+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.843",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFB3 were changed from to Mitochondrial complex I deficiency, nuclear type 25, MIM#618246",
"entity_name": "NDUFB3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:35:04.219840+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.842",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFB3 were set to ",
"entity_name": "NDUFB3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:34:52.622217+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.841",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFB3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFB3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:34:38.827164+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 22277967, 22499348, 27091925; Phenotypes: Mitochondrial complex I deficiency, nuclear type 25, MIM#618246; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFB3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:30:51.893943+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF6 as ready",
"entity_name": "NDUFAF6",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:30:51.886638+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf6 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF6",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:30:46.764047+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF6 were changed from to Mitochondrial complex I deficiency, nuclear type 17, MIM#618239",
"entity_name": "NDUFAF6",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:30:31.656426+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.839",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF6 were set to ",
"entity_name": "NDUFAF6",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:30:16.725173+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.838",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFAF6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF6",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:30:02.980969+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF6: Rating: GREEN; Mode of pathogenicity: None; Publications: 26741492, 18614015; Phenotypes: Mitochondrial complex I deficiency, nuclear type 17, MIM#618239; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF6",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:13:27.099321+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF4 as ready",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:13:27.092742+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf4 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:13:22.212847+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF4 were changed from to Mitochondrial complex I deficiency, nuclear type 15, MIM#618237",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:13:08.433446+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.836",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF4 were set to ",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:12:53.912724+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFAF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:12:39.745740+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: 18179882, 28853723; Phenotypes: Mitochondrial complex I deficiency, nuclear type 15, MIM#618237; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF4",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:10:31.585799+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF3 as ready",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:10:31.578125+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf3 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:10:26.806463+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF3 were changed from to Mitochondrial complex I deficiency, nuclear type 18, MIM#618240",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:10:12.477078+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF3 were set to ",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:09:59.953381+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.832",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFAF3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:09:46.353766+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF3: Rating: GREEN; Mode of pathogenicity: None; Publications: 19463981; Phenotypes: Mitochondrial complex I deficiency, nuclear type 18, MIM#618240; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF3",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:06:58.752541+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF2 as ready",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:06:58.745192+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf2 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:06:54.555780+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF2 were changed from to Mitochondrial complex I deficiency, nuclear type 10, MIM#618233",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:06:37.302921+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF2 were set to ",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:05:16.591660+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:05:01.201784+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mitochondrial complex I deficiency, nuclear type 10, MIM#618233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2019-12-07T19:02:39.688756+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17557076, 21931170, 24963768; Phenotypes: Mitochondrial complex I deficiency, nuclear type 11, MIM#618234; Mode of inheritance: None",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:58:29.276231+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFA9 as ready",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:58:29.269506+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa9 has been classified as Green List (High Evidence).",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:58:17.047969+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFA9 were changed from to Mitochondrial complex I deficiency, nuclear type 26, MIM#618247",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:58:04.262509+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFA9 were set to ",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:57:52.642035+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.826",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:57:36.928517+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFA9: Rating: GREEN; Mode of pathogenicity: None; Publications: 28671271, 22114105; Phenotypes: Mitochondrial complex I deficiency, nuclear type 26, MIM#618247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:23:02.149149+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFA2: Rating: GREEN; Mode of pathogenicity: None; Publications: 18513682, 28857146; Phenotypes: Mitochondrial complex I deficiency, nuclear type 13, MIM#618235; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA2",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:19:08.619577+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFA11 as ready",
"entity_name": "NDUFA11",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:19:08.612391+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFA11",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:19:03.926454+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFA11 were changed from to Mitochondrial complex I deficiency, nuclear type 14, MIM#618236",
"entity_name": "NDUFA11",
"entity_type": "gene"
}
]
}