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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1631",
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"results": [
{
"created": "2020-08-29T13:11:06.565961+10:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TMEM5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:10:42.695672+10:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TMEM5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23217329, 23519211; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, MIM# 615041; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:09:20.486233+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3985",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM5 as ready",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:09:20.476198+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3985",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem5 has been classified as Green List (High Evidence).",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:09:13.834054+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3985",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM5 were changed from to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, MIM# 615041",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:08:56.775443+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3984",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM5 were set to ",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:08:38.727689+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3983",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TMEM5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:08:21.715568+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3982",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TMEM5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23217329, 23519211; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, MIM# 615041; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:06:29.295708+10:00",
"panel_name": "Cobblestone Malformations",
"panel_id": 6,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM5 as ready",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:06:29.286321+10:00",
"panel_name": "Cobblestone Malformations",
"panel_id": 6,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem5 has been classified as Green List (High Evidence).",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:06:26.992795+10:00",
"panel_name": "Cobblestone Malformations",
"panel_id": 6,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM5 were changed from to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, MIM# 615041",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:06:06.491781+10:00",
"panel_name": "Cobblestone Malformations",
"panel_id": 6,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM5 were set to ",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:05:28.372063+10:00",
"panel_name": "Cobblestone Malformations",
"panel_id": 6,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TMEM5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:04:56.149941+10:00",
"panel_name": "Cobblestone Malformations",
"panel_id": 6,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TMEM5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23217329, 23519211; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, MIM# 615041; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:04:13.588938+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM5 as ready",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:04:13.577394+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem5 has been classified as Green List (High Evidence).",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:03:46.606086+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM5 were changed from to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, MIM# 615041",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:03:25.947665+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM5 were set to ",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:03:00.047232+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TMEM5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:02:30.255061+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TMEM5: Changed publications: 23217329, 23519211",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T13:01:59.217620+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TMEM5: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, MIM# 615041; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:37:27.985803+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF5C as ready",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:37:27.976678+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5c has been classified as Green List (High Evidence).",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:37:24.831622+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF5C were changed from to Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:37:08.370858+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF5C were set to ",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:36:43.540000+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.199",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF5C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:36:19.868918+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF5C: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 23033978, 32562872; Phenotypes: Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:35:41.147824+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2891",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF5C as ready",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:35:41.138948+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2891",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5c has been classified as Green List (High Evidence).",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:35:37.156649+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2891",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF5C were changed from to Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:34:31.008463+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2890",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF5C were set to ",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:34:28.297168+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF5C as ready",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:34:28.287152+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5c has been classified as Green List (High Evidence).",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:34:07.590505+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2889",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF5C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:33:37.641213+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF5C were changed from to Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:33:37.637664+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.2888",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF5C: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 23033978, 32562872; Phenotypes: Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:33:16.588449+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF5C were set to ",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:32:38.913818+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.814",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF5C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:32:26.687578+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3982",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF5C as ready",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:32:26.678173+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3982",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5c has been classified as Green List (High Evidence).",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:32:11.225128+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF5C: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 23033978, 32562872; Phenotypes: Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:31:23.307483+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3982",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF5C were changed from to Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:30:42.322223+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3981",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF5C were set to ",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:30:25.317742+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3980",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF5C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:30:07.268810+10:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF5C as ready",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:30:07.258119+10:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5c has been classified as Green List (High Evidence).",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:30:04.848363+10:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF5C were changed from to Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:29:37.349750+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF5C: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 23033978, 32562872; Phenotypes: Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:29:31.242989+10:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF5C were set to ",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:28:50.431877+10:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF5C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:28:25.105172+10:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF5C: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 23033978, 32562872; Phenotypes: Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:05:53.942795+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF5C as ready",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:05:53.934664+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5c has been classified as Green List (High Evidence).",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:05:51.776408+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF5C were changed from to Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:05:31.391155+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF5C were set to ",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:03:53.145158+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF5C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T12:03:25.091995+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF5C: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 23033978, 32562872; Phenotypes: Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:52:38.022742+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF2A as ready",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:52:38.010961+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif2a has been classified as Red List (Low Evidence).",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:52:33.782604+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF2A were changed from to Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:48:52.749372+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF2A were set to ",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:48:18.449150+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:47:57.594393+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIF2A as Red List (low evidence)",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:47:57.583992+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif2a has been classified as Red List (Low Evidence).",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:47:30.223990+10:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF2A: Rating: RED; Mode of pathogenicity: None; Publications: 23603762, 27896282, 27747449, 29077851, 31919497; Phenotypes: Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:45:38.803389+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF2A as ready",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:45:38.790429+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif2a has been classified as Green List (High Evidence).",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:45:35.124385+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIF2A as Green List (high evidence)",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:45:35.116433+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif2a has been classified as Green List (High Evidence).",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:45:12.105742+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KIF2A was added\ngene: KIF2A was added to Microcephaly. Sources: Expert Review\nMode of inheritance for gene: KIF2A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: KIF2A were set to 23603762; 27896282; 27747449; 29077851; 31919497\nPhenotypes for gene: KIF2A were set to Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411\nReview for gene: KIF2A was set to GREEN\nAdded comment: At least five unrelated families reported, with various malformations of cortical development including lissencephaly, agyria, posterior or frontal pachygyria, subcortical band heterotopia, and thin corpus callosum; microcephaly, intellectual disability and seizures. Microcephaly is in the range of -2SD -4.5SD, described as progressive in at least one individual. Some normocephalic but lower end of normal range. Some recurrent missense at p.Ser317 and p.His321. Functional data supports gene-disease association. \nSources: Expert Review",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:40:21.701380+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF2A as ready",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:40:21.693389+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif2a has been classified as Green List (High Evidence).",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:40:19.145688+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF2A were changed from to Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:39:53.555269+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.812",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF2A were set to ",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:39:31.668516+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:38:45.352594+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.810",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 27896282, 27747449, 29077851, 31919497; Phenotypes: Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:38:37.128947+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF2A as ready",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:38:37.119245+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif2a has been classified as Green List (High Evidence).",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:37:56.320463+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF2A as ready",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:37:56.312158+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif2a has been classified as Green List (High Evidence).",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:37:49.829346+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3979",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF2A were changed from to Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:37:33.330224+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3978",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF2A were set to ",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:37:16.760630+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:37:00.523148+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 27896282, 27747449, 29077851, 31919497; Phenotypes: Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:36:16.127322+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF2A were changed from to Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:35:50.843127+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF2A were set to ",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:35:24.766733+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:35:00.436972+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KIF2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23603762, 27896282, 27747449, 29077851, 31919497; Phenotypes: Cortical dysplasia, complex, with other brain malformations 3, MIM# 615411; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:28:57.647664+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DCX as ready",
"entity_name": "DCX",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:28:57.639895+10:00",
"panel_name": "Lissencephaly and Band Heterotopia",
"panel_id": 15,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dcx has been classified as Green List (High Evidence).",
"entity_name": "DCX",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:28:20.326808+10:00",
"panel_name": "Limb Girdle Muscular Dystrophy",
"panel_id": 3071,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ISPD as ready",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:28:20.316254+10:00",
"panel_name": "Limb Girdle Muscular Dystrophy",
"panel_id": 3071,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ispd has been classified as Green List (High Evidence).",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:28:17.403557+10:00",
"panel_name": "Limb Girdle Muscular Dystrophy",
"panel_id": 3071,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ISPD were set to ",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:28:05.131767+10:00",
"panel_name": "Limb Girdle Muscular Dystrophy",
"panel_id": 3071,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ISPD: Rating: GREEN; Mode of pathogenicity: None; Publications: 23390185, 30060766, 28688748, 26404900; Phenotypes: Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, MIM# 616052; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:26:08.441700+10:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ISPD as ready",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:26:08.431303+10:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ispd has been classified as Green List (High Evidence).",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:26:05.692393+10:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ISPD were changed from to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, MIM# 614643; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, MIM# 616052",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:25:30.375089+10:00",
"panel_name": "Hydrocephalus_Ventriculomegaly",
"panel_id": 115,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ISPD were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, MIM# 614643; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, MIM# 616052 to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, MIM# 614643",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:24:44.348330+10:00",
"panel_name": "Hydrocephalus_Ventriculomegaly",
"panel_id": 115,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ISPD were changed from to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, MIM# 614643; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, MIM# 616052",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2020-08-29T11:23:37.300441+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.3976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ISPD as ready",
"entity_name": "ISPD",
"entity_type": "gene"
}
]
}