All individuals with variants in gene NUP214

7 entries on 1 page. Showing entries 1 - 7.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00016306 - - family, 2 affected brothers M yes Palestine Palestinian - - - - ID cranio-lenticulo-sutural dysplasia (CLSD) and congenital disorders of glycosylation (CDG)-II 1 2 Swati Gupta
00240389 FamAPatIII3 PubMed: Fichtman 2019, Journal: Fichtman 2019 3-generation family, 2 affected (2M), unaffected heterozygous carrier parents/relatives F yes Palestine - - - - - ENC developmental delay; developmental regression; febrile-induced regression 21m; epilepsy; progressive microcephaly; no hypotonia; appendicular spasticity; ataxia; no myoclonic jerks; cerebellar atrophy; basal ganglia involvement; hyponatremia upon acute presentation 1 2 Johan den Dunnen
00240390 FamAPatIII12 PubMed: Fichtman 2019, Journal: Fichtman 2019 PatIII12 F yes Palestine - - - - - ENC developmental delay; developmental regression; febrile-induced regression 5m15d; no epilepsy; progressive microcephaly; hypotonia; myoclonic jerks; cerebellar atrophy; no basal ganglia involvement; hyponatremia upon acute presentation 1 1 Johan den Dunnen
00240391 FamBPatII1 PubMed: Fichtman 2019, Journal: Fichtman 2019 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents F no - Europe, north (non-Finland) - - - - ENC developmental delay; developmental regression; febrile-induced regression 15m; epilepsy; progressive microcephaly; hypotonia; ataxia; myoclonic jerks; cerebellar atrophy; no basal ganglia involvement; hyponatremia upon acute presentation 2 2 Johan den Dunnen
00240392 FamBPatII2 PubMed: Fichtman 2019, Journal: Fichtman 2019 sister PatII2 F no - Europe, north (non-Finland) - - - - ENC developmental delay; developmental regression; febrile-induced regression 30m; epilepsy; progressive microcephaly; hypotonia; ataxia; myoclonic jerks; cerebellar atrophy; no basal ganglia involvement; hyponatremia upon acute presentation 2 1 Johan den Dunnen
00314877 Trio44 PubMed: Zhu 2015 - F - United States - - - - - ? Peter’s anomaly bilaterally with microphthalmia, more on the right than the left, bilateral choanal atresia, communicating hydrocephalus, bilateral hearing loss requiring cochlear implants and acute lymphoblastic leukemia that has been in remission. 2 1 Johan den Dunnen
00465864 FamW10-3099 PubMed: Iqbal 2015 2-generation family, 3 affected, unaffected parents F - Netherlands - - - - - ID dsee paper; ..., moderate-severe intellectual disability; neonatal period cried excessively; psychomotor development delayed; progressive tremor; small hand length 2 3 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.