HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220504,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2029",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2027",
"results": [
{
"created": "2019-12-24T10:34:07.710122+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CWC27 was added\ngene: CWC27 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CWC27 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CWC27 were set to Retinitis pigmentosa with or without skeletal anomalies, 250410",
"entity_name": "CWC27",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.642296+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CRB1 was added\ngene: CRB1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CRB1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CRB1 were set to Pigmented paravenous chorioretinal atrophy, 172870; Leber congenital amaurosis 8, 613835; Retinitis pigmentosa-12, autosomal recessive, 600105",
"entity_name": "CRB1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.576323+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CNGB1 was added\ngene: CNGB1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CNGB1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CNGB1 were set to Retinitis pigmentosa 45, 613767",
"entity_name": "CNGB1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.506481+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CNGA1 was added\ngene: CNGA1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CNGA1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: CNGA1 were set to Retinitis pigmentosa 49, 613756",
"entity_name": "CNGA1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.435392+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CLRN1 was added\ngene: CLRN1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CLRN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CLRN1 were set to Retinitis pigmentosa 61, 614180",
"entity_name": "CLRN1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.367982+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CLN3 was added\ngene: CLN3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CLN3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CLN3 were set to Retinitis pigmentosa; Juvenile neuronal ceroid lipofuscinosis",
"entity_name": "CLN3",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.300895+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CLCC1 was added\ngene: CLCC1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CLCC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CLCC1 were set to 30157172\nPhenotypes for gene: CLCC1 were set to Retinitis pigmentosa 32",
"entity_name": "CLCC1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.234626+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CHM was added\ngene: CHM was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CHM was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPhenotypes for gene: CHM were set to Retinitis pigmentosa; Choroideremia (degeneration of the choriocapillaris, the retinal pigment epithelium, and the photoreceptor of the eye)",
"entity_name": "CHM",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.164091+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CERKL was added\ngene: CERKL was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CERKL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CERKL were set to Retinitis pigmentosa 26, 608380",
"entity_name": "CERKL",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.097611+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CEP290 was added\ngene: CEP290 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CEP290 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CEP290 were set to Senior-Loken syndrome 6, 610189; Meckel syndrome 4, 611134; Leber congenital amaurosis 10, 611755; Joubert syndrome 5, 610188; Bardet-Biedl syndrome 14, 209900",
"entity_name": "CEP290",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:07.031754+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: CDHR1 was added\ngene: CDHR1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CDHR1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CDHR1 were set to Achromatopsia, Cone, and Cone-rod Dystrophy; Cone-Rod Dystrophy, Recessive; Retinitis pigmentosa 65; Cone-rod dystrophy 15, 613660",
"entity_name": "CDHR1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.966368+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: C8orf37 was added\ngene: C8orf37 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: C8orf37 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: C8orf37 were set to Achromatopsia, Cone, and Cone-rod Dystrophy; Retinitis pigmentosa 64, 614500",
"entity_name": "C8orf37",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.901037+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: BEST1 was added\ngene: BEST1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: BEST1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: BEST1 were set to Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma, 1; Maculopathy, bull's-eye; Best Vitelliform Macular Dystrophy; Best macular dystrophy, 153700; Vitreoretinochoroidopathy, 193220; Retinitis pigmentosa; Retinitis Pigmentosa, Recessive; Bestrophinopathy, 611809; Vitelliform macular dystrophy, adult-onset, 608161",
"entity_name": "BEST1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.837018+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: BBS2 was added\ngene: BBS2 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: BBS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: BBS2 were set to Bardet-Biedl syndrome 2; Retinitis pigmentosa 74",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.769521+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: BBS1 was added\ngene: BBS1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: BBS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: BBS1 were set to Retinitis pigmentosa",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.701843+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ARL6 was added\ngene: ARL6 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARL6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARL6 were set to Retinitis pigmentosa 55, 613575; Bardet-Biedl syndrome 3, 209900",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.636453+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ARL2BP was added\ngene: ARL2BP was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARL2BP was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARL2BP were set to Retinitis pigmentosa with or without situs inversus, 615434",
"entity_name": "ARL2BP",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.563817+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ARHGEF18 was added\ngene: ARHGEF18 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARHGEF18 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARHGEF18 were set to Retinitis pigmentosa 78 617433",
"entity_name": "ARHGEF18",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.494891+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: AIPL1 was added\ngene: AIPL1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AIPL1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AIPL1 were set to Retinitis pigmentosa, juvenile; Leber congenital amaurosis 4; Cone-rod dystrophy",
"entity_name": "AIPL1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.428062+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: AHR was added\ngene: AHR was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AHR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AHR were set to 29726989\nPhenotypes for gene: AHR were set to ?Retinitis pigmentosa 85",
"entity_name": "AHR",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.362949+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: AHI1 was added\ngene: AHI1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AHI1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AHI1 were set to Joubert syndrome 17",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.295028+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: AGBL5 was added\ngene: AGBL5 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AGBL5 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AGBL5 were set to Retinitis pigmentosa 75 617023",
"entity_name": "AGBL5",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.231216+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ADGRA3 was added\ngene: ADGRA3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Red\nMode of inheritance for gene: ADGRA3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ADGRA3 were set to 23105016\nPhenotypes for gene: ADGRA3 were set to retinal dystrophy",
"entity_name": "ADGRA3",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.164647+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ABHD12 was added\ngene: ABHD12 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ABHD12 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABHD12 were set to Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa andCataract (PHARC); Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract, 614857",
"entity_name": "ABHD12",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:06.101366+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ABCA4 was added\ngene: ABCA4 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ABCA4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABCA4 were set to Macular Degeneration (Dominant); Stargardt disease 1, 248200; Macular degeneration, age-related, 2, 153800; Achromatopsia, Cone, and Cone-rod Dystrophy; Retinal dystrophy, early-onset severe, 248200; Stargardt Disease, Recessive; Retinitis pigmentosa 19, 601718; Cone-rod dystrophy 3, 604116; Macular Dystrophy/Degeneration/Stargardt Disease; Fundus flavimaculatus, 248200",
"entity_name": "ABCA4",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:05.960581+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ARL3 was added\ngene: ARL3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARL3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: ARL3 were set to 26936825; 16565502; 26964041; 26814127; 30932721; 30269812\nPhenotypes for gene: ARL3 were set to Retinitis pigmentosa 83; Joubert syndrome 35",
"entity_name": "ARL3",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:05.892856+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: ADIPOR1 was added\ngene: ADIPOR1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: ADIPOR1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: ADIPOR1 were set to 26662040; 25736573; 30254279; 27655171\nPhenotypes for gene: ADIPOR1 were set to syndromic retinitis pigmentosa; non-syndromic autosomal dominant retinitis pigmentosa",
"entity_name": "ADIPOR1",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:34:05.849428+11:00",
"panel_name": "Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"panel_id": 277,
"panel_version": "0.0",
"user_name": "Bryony Thompson",
"item_type": "panel",
"text": "Added panel Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-12-24T10:27:01.167488+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: INSRR as ready",
"entity_name": "INSRR",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:27:01.156202+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: insrr has been classified as Red List (Low Evidence).",
"entity_name": "INSRR",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:26:51.914075+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: INSRR as Red List (low evidence)",
"entity_name": "INSRR",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:26:51.909185+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Agreed, cannot find evidence for Mendelian gene-disease association.",
"entity_name": "INSRR",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:26:51.867063+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: insrr has been classified as Red List (Low Evidence).",
"entity_name": "INSRR",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:17:46.291675+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.413",
"user_name": "Lauren Akesson",
"item_type": "entity",
"text": "reviewed gene: INSRR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "INSRR",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:09:57.324110+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GRIK5 as ready",
"entity_name": "GRIK5",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:09:57.313044+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: grik5 has been classified as Red List (Low Evidence).",
"entity_name": "GRIK5",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:09:45.231475+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GRIK5 as Red List (low evidence)",
"entity_name": "GRIK5",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:09:45.220445+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Agreed, cannot find evidence for Mendelian gene-disease association.",
"entity_name": "GRIK5",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:09:44.976009+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: grik5 has been classified as Red List (Low Evidence).",
"entity_name": "GRIK5",
"entity_type": "gene"
},
{
"created": "2019-12-24T10:03:18.767355+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.412",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: GRIK5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "GRIK5",
"entity_type": "gene"
},
{
"created": "2019-12-24T09:20:57.186949+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MAGI2 as ready",
"entity_name": "MAGI2",
"entity_type": "gene"
},
{
"created": "2019-12-24T09:20:57.176145+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: magi2 has been classified as Green List (High Evidence).",
"entity_name": "MAGI2",
"entity_type": "gene"
},
{
"created": "2019-12-24T09:20:53.590026+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MAGI2 were changed from to Nephrotic syndrome, type 15, MIM# 617609",
"entity_name": "MAGI2",
"entity_type": "gene"
},
{
"created": "2019-12-24T09:20:28.021531+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MAGI2 were set to ",
"entity_name": "MAGI2",
"entity_type": "gene"
},
{
"created": "2019-12-24T09:19:58.070214+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MAGI2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MAGI2",
"entity_type": "gene"
},
{
"created": "2019-12-24T09:19:25.372357+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MAGI2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27932480, 25271328, 25108225; Phenotypes: Nephrotic syndrome, type 15, MIM# 617609; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MAGI2",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:30:07.543461+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CD151 as ready",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:30:07.532570+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd151 has been classified as Green List (High Evidence).",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:30:01.421379+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CD151 as Green List (high evidence)",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:30:01.402584+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd151 has been classified as Green List (High Evidence).",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:29:27.812142+11:00",
"panel_name": "Deafness_MelbourneGenomics_VCGS",
"panel_id": 209,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CD151 was added\ngene: CD151 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: CD151 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CD151 were set to 15265795; 29138120\nPhenotypes for gene: CD151 were set to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057\nReview for gene: CD151 was set to GREEN\nAdded comment: Three families described in the literature. \nSources: Literature",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:27:27.214532+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CD151 as ready",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:27:27.203698+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd151 has been classified as Green List (High Evidence).",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:27:22.053159+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CD151 as Green List (high evidence)",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:27:22.042396+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd151 has been classified as Green List (High Evidence).",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:26:40.571617+11:00",
"panel_name": "Epidermolysis bullosa_VCGS",
"panel_id": 101,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CD151 was added\ngene: CD151 was added to Epidermolysis bullosa_VCGS. Sources: Literature\nMode of inheritance for gene: CD151 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CD151 were set to 15265795; 29138120\nPhenotypes for gene: CD151 were set to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057\nAdded comment: Three families described in the literature \nSources: Literature",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:25:00.582101+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CD151 as ready",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:25:00.570648+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd151 has been classified as Green List (High Evidence).",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:24:56.131430+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CD151 as Green List (high evidence)",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:24:56.117697+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd151 has been classified as Green List (High Evidence).",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:24:27.408347+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CD151 was added\ngene: CD151 was added to Proteinuria_VCGS_KidGen. Sources: Expert list\nMode of inheritance for gene: CD151 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CD151 were set to 15265795; 29138120\nPhenotypes for gene: CD151 were set to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057\nReview for gene: CD151 was set to GREEN\nAdded comment: Three families described in the literature. \nSources: Expert list",
"entity_name": "CD151",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:00:59.945337+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAN1 as ready",
"entity_name": "FAN1",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:00:59.934877+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fan1 has been classified as Green List (High Evidence).",
"entity_name": "FAN1",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:00:51.863147+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FAN1 as Green List (high evidence)",
"entity_name": "FAN1",
"entity_type": "gene"
},
{
"created": "2019-12-23T18:00:51.850152+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fan1 has been classified as Green List (High Evidence).",
"entity_name": "FAN1",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:04:42.735280+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D8B as ready",
"entity_name": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:04:42.727584+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d8b has been classified as Green List (High Evidence).",
"entity_name": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:04:21.763008+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D8B were changed from to Nephrotic syndrome, type 20, MIM# 301028",
"entity_name": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:04:08.496383+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.411",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D8B were set to ",
"entity_name": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:03:50.057407+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.410",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPST as ready",
"entity_name": "MPST",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:03:50.050826+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.410",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpst has been classified as Red List (Low Evidence).",
"entity_name": "MPST",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:03:39.540758+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.410",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MPST as Red List (low evidence)",
"entity_name": "MPST",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:03:39.533667+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.410",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpst has been classified as Red List (Low Evidence).",
"entity_name": "MPST",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:02:42.183221+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.409",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: MPST: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "MPST",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:02:33.595937+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.409",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBC1D8B 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": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:02:14.732025+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBC1D8B: Rating: GREEN; Mode of pathogenicity: None; Publications: 30661770; Phenotypes: Nephrotic syndrome, type 20, MIM# 301028; 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": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:00:48.230621+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D8B were changed from to Nephrotic syndrome, type 20, MIM# 301028",
"entity_name": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T16:00:23.583917+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D8B were set to ",
"entity_name": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:59:57.908917+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBC1D8B 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": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:59:11.908183+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.54",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: TBC1D8B: Rating: GREEN; Mode of pathogenicity: None; Publications: 30661770; Phenotypes: Nephrotic syndrome, type 20, MIM# 301028; 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": "TBC1D8B",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:55:37.554121+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ANKRD17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ANKRD17",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:54:40.190296+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIM24 as ready",
"entity_name": "TRIM24",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:54:40.181848+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim24 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM24",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:54:29.310097+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIM24 as Red List (low evidence)",
"entity_name": "TRIM24",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:54:29.302197+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.407",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim24 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM24",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:53:33.356226+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.406",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: TRIM24: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "TRIM24",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:50:04.195085+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.406",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARID5B as ready",
"entity_name": "ARID5B",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:50:04.188210+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.406",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arid5b has been classified as Red List (Low Evidence).",
"entity_name": "ARID5B",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:49:55.250429+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.406",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ARID5B as Red List (low evidence)",
"entity_name": "ARID5B",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:49:55.243101+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.406",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arid5b has been classified as Red List (Low Evidence).",
"entity_name": "ARID5B",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:49:18.222952+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.405",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: ARID5B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "ARID5B",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:46:13.583639+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MLX as ready",
"entity_name": "MLX",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:46:13.576929+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlx has been classified as Red List (Low Evidence).",
"entity_name": "MLX",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:46:03.189875+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MLX as Red List (low evidence)",
"entity_name": "MLX",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:46:03.181120+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.405",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlx has been classified as Red List (Low Evidence).",
"entity_name": "MLX",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:45:27.877849+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.404",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: MLX: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "MLX",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:42:12.636127+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.404",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: REV3L as ready",
"entity_name": "REV3L",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:42:12.629068+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.404",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rev3l has been classified as Green List (High Evidence).",
"entity_name": "REV3L",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:42:04.236948+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.404",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: REV3L were changed from to Moebius syndrome",
"entity_name": "REV3L",
"entity_type": "gene"
},
{
"created": "2019-12-23T15:41:49.478604+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.403",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: REV3L were set to ",
"entity_name": "REV3L",
"entity_type": "gene"
}
]
}