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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1722",
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"results": [
{
"created": "2020-07-21T23:00:02.721401+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DDX59 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DDX59",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:59:36.696650+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CSPP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CSPP1",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:59:12.086769+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CKAP2L was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CKAP2L",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:58:47.500355+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CEP41 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CEP41",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:58:21.965853+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CEP290 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CEP290",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:57:58.162760+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CEP164 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CEP164",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:57:34.253482+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CEP120 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CEP120",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:57:02.717726+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CENPF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CENPF",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:56:31.595997+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CCND2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CCND2",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:56:00.919859+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CC2D2A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CC2D2A",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:55:26.153865+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: C5orf42 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "C5orf42",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:55:01.646952+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: C2CD3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "C2CD3",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:54:34.116026+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BMP4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BMP4",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:54:07.555352+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BHLHA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:53:38.001493+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS9",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:52:05.502062+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS7",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:51:36.544563+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS5",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:51:07.888801+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS4",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:50:38.505190+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:50:09.284651+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:49:04.886570+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS10 as ready",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:49:04.876446+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs10 has been classified as Green List (High Evidence).",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:48:59.986059+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:48:36.205373+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS1 as ready",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:48:36.198661+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs1 has been classified as Green List (High Evidence).",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:48:33.481258+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS1 were changed from to Bardet-Biedl syndrome 1, MIM#\t209900",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:47:49.636119+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:47:02.144602+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARL6 as ready",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:47:02.137244+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arl6 has been classified as Green List (High Evidence).",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:46:56.631111+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ARL6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ARL6",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:46:12.001228+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AKT3 as ready",
"entity_name": "AKT3",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:46:11.991549+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akt3 has been classified as Green List (High Evidence).",
"entity_name": "AKT3",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:46:09.043388+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AKT3 were changed from to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM#\t615937",
"entity_name": "AKT3",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:45:44.626142+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AKT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "AKT3",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:45:12.074194+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AHI1 as ready",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:45:12.065099+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ahi1 has been classified as Green List (High Evidence).",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:45:07.320663+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AHI1 were changed from to Joubert syndrome 3, MIM#\t608629",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2020-07-21T22:44:22.924867+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AHI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2020-07-21T20:47:18.624268+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.367",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Deafness_ComplexAndIsolated to Deafness_IsolatedAndComplex",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-07-21T20:45:44.978372+10:00",
"panel_name": "Deafness_ComplexAndIsolated",
"panel_id": 209,
"panel_version": "0.366",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Deafness to Deafness_ComplexAndIsolated",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-07-21T14:26:15.183597+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: ALX3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:25:55.761418+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: ALMS1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:25:29.642418+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: PDE6D: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:24:59.700123+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: CD96: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CD96",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:24:37.267758+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: ZSWIM6: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZSWIM6",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:24:22.056400+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: ZNF141: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZNF141",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:24:11.980284+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: WNT7A: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:23:57.409495+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: WDR60: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR60",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:23:43.875988+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: WDR35: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR35",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:23:31.349642+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: WDR34: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:23:19.604620+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: WDR19: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:23:03.060503+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: WDPCP: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDPCP",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:22:37.747390+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: USP9X: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; 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": "USP9X",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:22:19.426954+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: UBE3B: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UBE3B",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:22:03.626641+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TWIST1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:21:45.838984+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TTC8: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:21:28.257620+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TTC21B: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:21:08.295855+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TRAF3IP1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRAF3IP1",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:20:50.816623+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TMEM67: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:20:35.849007+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TMEM237: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM237",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:20:21.222152+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TMEM231: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM231",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:20:07.783960+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TMEM216: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM216",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:19:37.957533+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TMEM138: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM138",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:19:19.061933+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TFAP2B: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TFAP2B",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:19:02.107101+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TFAP2A: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TFAP2A",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:18:43.217497+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TCTN3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TCTN3",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:18:30.432110+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TCTN2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TCTN2",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:18:16.540321+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TCTEX1D2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TCTEX1D2",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:18:00.422699+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TBX5: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX5",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:17:45.800352+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TBX3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBX3",
"entity_type": "gene"
},
{
"created": "2020-07-21T14:17:29.456156+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: TBX22: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; 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": "TBX22",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:31:29.440475+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: SPINT2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPINT2",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:31:14.605997+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: SMOC1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SMOC1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:30:45.328530+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "edited their review of gene: SMO: Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "SMO",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:30:08.828054+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: SMO: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SMO",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:25:46.099837+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: SHH: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SHH",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:25:28.974958+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: SDCCAG8: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SDCCAG8",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:25:06.422778+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: SC5D: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SC5D",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:24:53.224227+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: SALL4: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:24:39.648847+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: SALL1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:24:13.703623+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: RPGRIP1L: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RPGRIP1L",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:24:00.156275+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: RBM10: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RBM10",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:23:43.374016+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: RAB23: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "RAB23",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:23:30.739396+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: PROM1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "PROM1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:22:58.769214+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: PORCN: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; 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": "PORCN",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:22:26.820144+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: PNPLA6: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PNPLA6",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:22:01.170183+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: PITX1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PITX1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:21:45.787131+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: PIK3R2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PIK3R2",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:21:20.637700+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: PIK3CA: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: Other",
"entity_name": "PIK3CA",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:20:03.318371+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: OFD1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; 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": "OFD1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:19:15.025566+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: NPHP3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NPHP3",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:19:01.258772+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: NEK1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:18:40.470208+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: MKS1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:18:25.488905+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: MKKS: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:18:10.692302+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: MEGF8: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MEGF8",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:17:47.725510+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: MBTPS2: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "MBTPS2",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:17:28.634532+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: LZTFL1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:17:12.698101+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: LRP4: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "LRP4",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:16:49.496287+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: LMBR1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "LMBR1",
"entity_type": "gene"
},
{
"created": "2020-07-21T13:16:29.981179+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.36",
"user_name": "Anand Vasudevan",
"item_type": "entity",
"text": "reviewed gene: LBR: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "LBR",
"entity_type": "gene"
}
]
}