HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220212,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=882",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=880",
"results": [
{
"created": "2022-04-16T15:35:56.376742+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRPH were set to ",
"entity_name": "PRPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:35:40.292279+10:00",
"panel_name": "Motor Neurone Disease",
"panel_id": 25,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRPH was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PRPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:35:19.845612+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12971",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRPH was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PRPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:35:13.124428+10:00",
"panel_name": "Motor Neurone Disease",
"panel_id": 25,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRPH was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PRPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:34:53.409083+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRPH as Amber List (moderate evidence)",
"entity_name": "PRPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:34:53.398727+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prph has been classified as Amber List (Moderate Evidence).",
"entity_name": "PRPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:34:10.811407+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRPH: Rating: AMBER; Mode of pathogenicity: None; Publications: 20363051, 15322088, 15446584; Phenotypes: {Amyotrophic lateral sclerosis, susceptibility to}, 105400; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PRPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:32:12.754689+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRSS1 as ready",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:32:12.745493+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prss1 has been classified as Green List (High Evidence).",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:32:03.259897+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRSS1 were changed from to Pancreatitis, hereditary, MIM# 167800",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:31:39.464257+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRSS1 were set to ",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:31:16.491495+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12967",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRSS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:30:55.214313+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: PRSS1.",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:30:42.418759+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRSS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 8841182, 10204851, 10529393, 11097832, 11702203, 15776435, 16791840, 18461367, 17072318; Phenotypes: Pancreatitis, hereditary, MIM# 167800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PRSS1",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:29:07.138659+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRSS12 as ready",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:29:07.128759+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prss12 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:28:59.874460+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRSS12 were changed from to Intellectual disability, PRSS12 related MIM#249500",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:28:20.153291+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRSS12 were set to ",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:27:47.609869+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRSS12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:27:15.996965+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRSS12 as Amber List (moderate evidence)",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:27:15.984752+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prss12 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:26:42.644744+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRSS12: Rating: AMBER; Mode of pathogenicity: None; Publications: 12459588; Phenotypes: Intellectual disability, PRSS12 related MIM#249500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:25:28.599976+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRSS12 as ready",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:25:28.590620+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prss12 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:25:16.343200+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRSS12 were changed from to Intellectual disability, PRSS12 related MIM#249500",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:24:50.735804+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12965",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PRSS12 were set to ",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:24:03.713540+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PRSS12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:23:42.914742+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRSS12 as Amber List (moderate evidence)",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:23:42.902242+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prss12 has been classified as Amber List (Moderate Evidence).",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:22:38.855221+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRSS12: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Intellectual disability, PRSS12 related MIM#249500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PRSS12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:17:25.979748+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSMC2 as ready",
"entity_name": "PSMC2",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:17:25.969905+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psmc2 has been classified as Red List (Low Evidence).",
"entity_name": "PSMC2",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:17:16.135430+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PSMC2 as Red List (low evidence)",
"entity_name": "PSMC2",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:17:16.123878+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psmc2 has been classified as Red List (Low Evidence).",
"entity_name": "PSMC2",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:16:56.440025+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PSMC2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "PSMC2",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:55.937803+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSMC3IP as ready",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:55.928770+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psmc3ip has been classified as Green List (High Evidence).",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:50.850370+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.295",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSMC3IP as ready",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:50.838364+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.295",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psmc3ip has been classified as Green List (High Evidence).",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:48.180210+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.295",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PSMC3IP were changed from Ovarian dysgenesis 3,614324 to Ovarian dysgenesis 3, MIM# 614324",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:38.148048+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.294",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PSMC3IP were set to ",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:30.340331+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PSMC3IP were changed from to Ovarian dysgenesis 3, MIM# 614324",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:19.110425+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.293",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PSMC3IP: Rating: GREEN; Mode of pathogenicity: None; Publications: 21963259, 35352317, 34878148, 30406445, 29240891; Phenotypes: Ovarian dysgenesis 3, MIM# 614324; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:14:07.130852+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PSMC3IP were set to ",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:13:51.102090+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PSMC3IP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:13:07.740871+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PSMC3IP: Rating: GREEN; Mode of pathogenicity: None; Publications: 21963259, 35352317, 34878148, 30406445, 29240891; Phenotypes: Ovarian dysgenesis 3, MIM# 614324; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PSMC3IP",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:03:27.950924+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSMD12 as ready",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:03:27.939683+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psmd12 has been classified as Green List (High Evidence).",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:03:22.629842+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PSMD12 were changed from to Stankiewicz-Isidor syndrome, MIM# 617516",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:02:53.588289+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PSMD12 were set to ",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:02:26.461130+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PSMD12 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:01:51.532088+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PSMD12: Rating: GREEN; Mode of pathogenicity: None; Publications: 28132691, 34906456; Phenotypes: Stankiewicz-Isidor syndrome, MIM# 617516; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:01:17.225961+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSMD12 as ready",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:01:17.211901+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psmd12 has been classified as Green List (High Evidence).",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:01:02.853332+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PSMD12 were changed from to Stankiewicz-Isidor syndrome, MIM# 617516",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:00:41.506721+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12957",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PSMD12 were set to ",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T15:00:20.317810+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PSMD12 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:59:59.245940+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12955",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PSMD12: Rating: GREEN; Mode of pathogenicity: None; Publications: 28132691, 34906456; Phenotypes: Stankiewicz-Isidor syndrome, MIM# 617516; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PSMD12",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:55:43.730750+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12955",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSPH as ready",
"entity_name": "PSPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:55:43.717663+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12955",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psph has been classified as Green List (High Evidence).",
"entity_name": "PSPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:55:21.766488+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12955",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PSPH were changed from to Phosphoserine phosphatase deficiency MIM#614023; Disorders of serine, glycine or glycerate metabolism",
"entity_name": "PSPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:54:58.446515+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12954",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PSPH were set to ",
"entity_name": "PSPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:54:37.946357+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12953",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PSPH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PSPH",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:53:50.990157+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSTPIP1 as ready",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:53:50.977577+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pstpip1 has been classified as Green List (High Evidence).",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:53:44.984763+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PSTPIP1 were changed from to Pyogenic sterile arthritis, pyoderma gangrenosum, and acne, MIM# 604416; PSTPIP1-associated myeloid-related proteinemia inflammatory (PAMI) syndrome",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:53:13.306975+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PSTPIP1 were set to ",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:52:36.541401+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PSTPIP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:52:04.794583+10:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PSTPIP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11971877, 34938582, 34778321, 34745107, 34492165, 34047005; Phenotypes: Pyogenic sterile arthritis, pyoderma gangrenosum, and acne, MIM# 604416, PSTPIP1-associated myeloid-related proteinemia inflammatory (PAMI) syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:50:59.879785+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12952",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSTPIP1 as ready",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:50:59.870694+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12952",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pstpip1 has been classified as Green List (High Evidence).",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:50:39.998855+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12952",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PSTPIP1 were changed from to Pyogenic sterile arthritis, pyoderma gangrenosum, and acne, MIM# 604416; PSTPIP1-associated myeloid-related proteinemia inflammatory (PAMI) syndrome",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:50:19.170851+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12951",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PSTPIP1 were set to ",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:49:51.129992+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PSTPIP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T14:49:29.503114+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PSTPIP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11971877, 34938582, 34778321, 34745107, 34492165, 34047005; Phenotypes: Pyogenic sterile arthritis, pyoderma gangrenosum, and acne, MIM# 604416, PSTPIP1-associated myeloid-related proteinemia inflammatory (PAMI) syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PSTPIP1",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:52:23.964917+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTGDR as ready",
"entity_name": "PTGDR",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:52:23.951302+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptgdr has been classified as Red List (Low Evidence).",
"entity_name": "PTGDR",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:52:14.331430+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTGDR were changed from to {Asthma, susceptibility to, 1} 607277",
"entity_name": "PTGDR",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:51:54.096587+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12948",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PTGDR was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTGDR",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:51:34.578902+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PTGDR as Red List (low evidence)",
"entity_name": "PTGDR",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:51:34.566447+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptgdr has been classified as Red List (Low Evidence).",
"entity_name": "PTGDR",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:51:15.763544+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PTGDR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Asthma, susceptibility to, 1} 607277; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTGDR",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:49:02.274761+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTH as ready",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:49:02.265443+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pth has been classified as Green List (High Evidence).",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:48:52.989434+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTH were changed from to Hypoparathyroidism, familial isolated 1, MIM# 146200",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:48:27.107662+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12945",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PTH were set to ",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:48:04.283304+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12944",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PTH was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-04-16T10:47:44.470610+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PTH: Rating: GREEN; Mode of pathogenicity: None; Publications: 2212001, 1302009, 10523031, 35165722, 32421798; Phenotypes: Hypoparathyroidism, familial isolated 1, MIM# 146200; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:42:47.898391+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTH1R as ready",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:42:47.886465+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pth1r has been classified as Green List (High Evidence).",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:42:38.339168+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTH1R were changed from to Failure of tooth eruption, primary MIM#125350; Eiken syndrome MIM#600002; Metaphyseal chondrodysplasia, Murk Jansen type MIM#156400; Chondrodysplasia, Blomstrand type MIM#215045",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:42:17.880852+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12942",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PTH1R were set to ",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:41:55.242169+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12941",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PTH1R: Changed publications: 7701349, 8855805, 17164305, 15525660, 19061984",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:40:24.449165+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12941",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PTH1R was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:40:03.947401+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PTH1R: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Failure of tooth eruption, primary MIM#125350, Eiken syndrome MIM#600002, Metaphyseal chondrodysplasia, Murk Jansen type MIM#156400, Chondrodysplasia, Blomstrand type MIM#215045; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:34:55.820822+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTHLH as ready",
"entity_name": "PTHLH",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:34:55.797908+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pthlh has been classified as Green List (High Evidence).",
"entity_name": "PTHLH",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:32:33.873640+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTHLH were changed from to Brachydactyly, type E2, MIM# 613382",
"entity_name": "PTHLH",
"entity_type": "gene"
},
{
"created": "2022-04-15T13:32:10.589240+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12939",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PTHLH were set to ",
"entity_name": "PTHLH",
"entity_type": "gene"
},
{
"created": "2022-04-15T12:27:31.347943+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.12938",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PTHLH was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTHLH",
"entity_type": "gene"
}
]
}