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{
"count": 220725,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1563",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1561",
"results": [
{
"created": "2020-10-01T13:49:42.295553+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.533",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pax3 has been classified as Green List (High Evidence).",
"entity_name": "PAX3",
"entity_type": "gene"
},
{
"created": "2020-10-01T13:49:31.244921+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.533",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PAX3 were changed from to Waardenburg syndrome, type 1, MIM# 193500",
"entity_name": "PAX3",
"entity_type": "gene"
},
{
"created": "2020-10-01T13:49:04.521151+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.532",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PAX3 were set to ",
"entity_name": "PAX3",
"entity_type": "gene"
},
{
"created": "2020-10-01T13:48:29.446517+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PAX3 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "PAX3",
"entity_type": "gene"
},
{
"created": "2020-10-01T13:48:05.416577+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PAX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 27759048, 7897628, 28690861, 30314436, 25932447, 7726174, 12949970; Phenotypes: Waardenburg syndrome, type 1, MIM# 193500; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "PAX3",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:58:43.301390+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OTOGL as ready",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:58:43.252213+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: otogl has been classified as Green List (High Evidence).",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:58:36.596289+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OTOGL were changed from to Deafness, autosomal recessive 84B, MIM# 614944",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:57:26.965717+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4713",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OTOGL were set to ",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:57:07.852386+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OTOGL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:56:49.708377+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OTOGL: Rating: GREEN; Mode of pathogenicity: None; Publications: 23122586, 23850727, 25829320, 25719458, 28426234; Phenotypes: Deafness, autosomal recessive 84B, MIM# 614944; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:55:59.902269+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OTOGL as ready",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:55:59.887240+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: otogl has been classified as Green List (High Evidence).",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:55:56.881563+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OTOGL were changed from Deafness, autosomal recessive 84B, MIM# 614944 to Deafness, autosomal recessive 84B, MIM# 614944",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:55:42.855813+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OTOGL were changed from to Deafness, autosomal recessive 84B, MIM# 614944",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:55:21.796025+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.529",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OTOGL were set to ",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:54:56.720454+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OTOGL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:54:29.815833+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OTOGL: Rating: GREEN; Mode of pathogenicity: None; Publications: 23122586, 23850727, 25829320, 25719458, 28426234; Phenotypes: Deafness, autosomal recessive 84B, MIM# 614944; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OTOGL",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:51:55.146676+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RDX as ready",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:51:55.135411+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rdx has been classified as Green List (High Evidence).",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:51:51.842863+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RDX were changed from Deafness, autosomal recessive to Deafness, autosomal recessive 24, MIM# 611022",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:51:29.009904+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RDX were set to ",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:51:15.760388+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RDX as Green List (high evidence)",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:51:15.751974+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rdx has been classified as Green List (High Evidence).",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:51:03.508772+10:00",
"panel_name": "Newborn Screening_BabySeq",
"panel_id": 3302,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RDX: Rating: GREEN; Mode of pathogenicity: None; Publications: 17226784, 19215054, 22567349, 26226137, 15314067; Phenotypes: Deafness, autosomal recessive 24, MIM# 611022; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:49:30.858235+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RDX as ready",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:49:30.844687+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rdx has been classified as Green List (High Evidence).",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:49:24.364370+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RDX were changed from to Deafness, autosomal recessive 24, MIM# 611022",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:49:06.289381+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4710",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RDX were set to ",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:48:46.134563+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RDX was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:48:00.697891+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RDX: Rating: GREEN; Mode of pathogenicity: None; Publications: 17226784, 19215054, 22567349, 26226137, 15314067; Phenotypes: Deafness, autosomal recessive 24, MIM# 611022; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:47:17.511812+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RDX as ready",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:47:17.498168+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rdx has been classified as Green List (High Evidence).",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:46:46.665078+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RDX were changed from to Deafness, autosomal recessive 24, MIM# 611022",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:46:23.603058+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RDX were set to ",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:45:56.037243+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RDX was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:45:31.846193+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.524",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RDX: Rating: GREEN; Mode of pathogenicity: None; Publications: 17226784, 19215054, 22567349, 26226137, 15314067; Phenotypes: Deafness, autosomal recessive 24, MIM# 611022; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RDX",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:32:17.205602+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3038",
"user_name": "Ee Ming Wong",
"item_type": "entity",
"text": "reviewed gene: ARID2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 26238514; Phenotypes: neurodevelopmental delay, global developmental delay, gross motor delay; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "ARID2",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:20:47.447555+10:00",
"panel_name": "Progressive Neurological Conditions",
"panel_id": 3377,
"panel_version": "0.1",
"user_name": "Bryony Thompson",
"item_type": "panel",
"text": "Changed child panels to: Myopathy - paediatric onset; Ataxia - paediatric; Leukodystrophy - paediatric; Hereditary Spastic Paraplegia - paediatric; Dystonia - complex; Ataxia - adult onset; Early-onset Dementia; Motor Neuron Disease; Myopathy - adult onset; Early-onset Parkinson disease; Hereditary Neuropathy - complex; Leukodystrophy - adult onset; Limb Girdle Muscular Dystrophy; Hereditary Neuropathy_CMT - isolated; Brain Calcification; Hereditary Spastic Paraplegia - adult onset; Brain Channelopathies; Dystonia - isolated/combined",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-10-01T11:07:30.908445+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OTOA as ready",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:07:30.899314+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: otoa has been classified as Green List (High Evidence).",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:07:23.534015+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OTOA were changed from to Deafness, autosomal recessive 22, MIM# 607039",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:07:05.069214+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4707",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OTOA were set to ",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:06:27.125026+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OTOA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:06:11.133441+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OTOA: Rating: GREEN; Mode of pathogenicity: None; Publications: 11972037, 19888295, 23173898, 16460646, 26029705, 26969326, 23129639; Phenotypes: Deafness, autosomal recessive 22, MIM# 607039; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:05:17.967629+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.524",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OTOA as ready",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:05:17.959047+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.524",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: otoa has been classified as Green List (High Evidence).",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:05:15.775873+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.524",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OTOA were changed from to Deafness, autosomal recessive 22, MIM# 607039",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:04:47.812092+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OTOA were set to ",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:04:23.821517+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OTOA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T11:03:56.550102+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OTOA: Rating: GREEN; Mode of pathogenicity: None; Publications: 11972037, 19888295, 23173898, 16460646, 26029705, 26969326, 23129639; Phenotypes: Deafness, autosomal recessive 22, MIM# 607039; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OTOA",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:59:13.275551+10:00",
"panel_name": "Usher Syndrome",
"panel_id": 3086,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO7A as ready",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:59:13.267212+10:00",
"panel_name": "Usher Syndrome",
"panel_id": 3086,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo7a has been classified as Green List (High Evidence).",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:59:09.745764+10:00",
"panel_name": "Usher Syndrome",
"panel_id": 3086,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO7A were set to ",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:58:35.855981+10:00",
"panel_name": "Usher Syndrome",
"panel_id": 3086,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYO7A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23559863, 18181211, 25211151, 11391666; Phenotypes: Usher syndrome, type 1B, MIM# 276900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:56:26.150528+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO7A as ready",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:56:26.127354+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo7a has been classified as Green List (High Evidence).",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:56:08.822244+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO7A were changed from to Deafness, autosomal dominant 11, MIM# 601317; Deafness, autosomal recessive 2, 600060; Usher syndrome, type 1B, MIM# 276900",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:55:49.646562+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4704",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO7A were set to ",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:55:32.092780+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYO7A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:55:14.573121+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYO7A: Rating: GREEN; Mode of pathogenicity: None; Publications: 9354784, 15300860, 15121790, 15221449, 16449806, 21150918, 23451214, 23383098, 28802369, 29400105, 23559863, 18181211, 25211151; Phenotypes: Deafness, autosomal dominant 11, MIM# 601317, Deafness, autosomal recessive 2, 600060, Usher syndrome, type 1B, MIM# 276900; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:53:58.152687+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO7A as ready",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:53:58.142334+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo7a has been classified as Green List (High Evidence).",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:53:33.689897+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO7A were changed from to Deafness, autosomal dominant 11, MIM# 601317; Deafness, autosomal recessive 2, 600060; Usher syndrome, type 1B, MIM# 276900",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:52:59.019089+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO7A were set to ",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:52:31.704703+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.519",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYO7A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:51:59.843468+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYO7A: Rating: GREEN; Mode of pathogenicity: None; Publications: 9354784, 15300860, 15121790, 15221449, 16449806, 21150918, 23451214, 23383098, 28802369, 29400105, 23559863, 18181211, 25211151; Phenotypes: Deafness, autosomal dominant 11, MIM# 601317, Deafness, autosomal recessive 2, 600060, Usher syndrome, type 1B, MIM# 276900; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:33:27.126370+10:00",
"panel_name": "Progressive Neurological Conditions",
"panel_id": 3377,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "panel",
"text": "Added Panel Progressive Neurological Conditions\nSet child panels to: Myopathy - paediatric onset; Ataxia - paediatric; Leukodystrophy - paediatric; Hereditary Spastic Paraplegia - paediatric; Dystonia - complex; Ataxia - adult onset; Early-onset Dementia; Motor Neuron Disease; Myopathy - adult onset; Early-onset Parkinson disease; Hereditary Neuropathy - complex; Leukodystrophy - adult onset; Limb Girdle Muscular Dystrophy; Hereditary Neuropathy_CMT - isolated; Hereditary Spastic Paraplegia - adult onset; Dystonia - isolated/combined\nSet panel types to: Royal Melbourne Hospital; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-10-01T10:27:54.389850+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SMPX as ready",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:27:54.379050+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: smpx has been classified as Green List (High Evidence).",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:27:36.970866+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SMPX as ready",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:27:36.956658+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: smpx has been classified as Green List (High Evidence).",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:23:50.126698+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SMPX were changed from to Deafness, X-linked 4, MIM# 300066",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:23:31.384551+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4701",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SMPX were set to ",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:23:12.915701+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4700",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SMPX was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:22:57.411330+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4699",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SMPX: Rating: GREEN; Mode of pathogenicity: None; Publications: 21549342, 21549336, 21893181, 22911656, 28542515; Phenotypes: Deafness, X-linked 4, MIM# 300066; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:07:07.936995+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SMPX were changed from Deafness, X-linked 4, MIM# 300066 to Deafness, X-linked 4, MIM# 300066",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:06:31.110794+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.517",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SMPX were changed from to Deafness, X-linked 4, MIM# 300066",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:05:53.187692+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SMPX were set to ",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:05:25.497415+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SMPX was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:04:58.223920+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SMPX: Rating: GREEN; Mode of pathogenicity: None; Publications: 21549342, 21549336, 21893181, 22911656, 28542515; Phenotypes: Deafness, X-linked 4, MIM# 300066; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "SMPX",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:01:30.800525+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4699",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO6 as ready",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:01:30.790297+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4699",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo6 has been classified as Green List (High Evidence).",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:01:23.660185+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4699",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO6 were changed from to Deafness, autosomal dominant 22, MIM# 606346; Deafness, autosomal recessive 37, MIM# 607821",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:01:05.621751+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4698",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO6 were set to ",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:00:47.309163+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4697",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYO6 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T10:00:29.216693+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYO6: Rating: GREEN; Mode of pathogenicity: None; Publications: 24105371, 11468689, 25999546, 25227905, 18348273, 27171474; Phenotypes: Deafness, autosomal dominant 22, MIM# 606346, Deafness, autosomal recessive 37, MIM# 607821; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:59:41.645743+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO6 as ready",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:59:41.636733+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo6 has been classified as Green List (High Evidence).",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:59:03.420809+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO6 were changed from to Deafness, autosomal dominant 22, MIM# 606346; Deafness, autosomal recessive 37, MIM# 607821",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:58:23.541666+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.513",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO6 were set to ",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:57:47.865355+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYO6 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:57:24.199334+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYO6: Rating: GREEN; Mode of pathogenicity: None; Publications: 24105371, 11468689, 25999546, 25227905, 18348273, 27171474; Phenotypes: Deafness, autosomal dominant 22, MIM# 606346, Deafness, autosomal recessive 37, MIM# 607821; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "MYO6",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:51:25.768882+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO15A as ready",
"entity_name": "MYO15A",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:51:25.756187+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo15a has been classified as Green List (High Evidence).",
"entity_name": "MYO15A",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:51:17.355031+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO15A were changed from to Deafness, autosomal recessive 3, MIM# 600316",
"entity_name": "MYO15A",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:50:54.342185+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4695",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO15A were set to ",
"entity_name": "MYO15A",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:50:36.026216+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYO15A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYO15A",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:50:11.376050+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4693",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYO15A: Rating: GREEN; Mode of pathogenicity: None; Publications: 27375115, 26226137, 23208854, 19309289, 9603735, 10915760; Phenotypes: Deafness, autosomal recessive 3, MIM# 600316; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYO15A",
"entity_type": "gene"
},
{
"created": "2020-10-01T09:49:15.771810+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO15A as ready",
"entity_name": "MYO15A",
"entity_type": "gene"
}
]
}