All individuals with variants in gene TSEN54

18 entries on 1 page. Showing entries 1 - 18.
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     
00180168 29286531-Pat20 PubMed: TumienÄ— 2018 - - - (Slovenia) - - - - - ? Epilepsy (HP:0001250), focal seizures (HP:0007359), severe global developmental delay (HP:0011344). Head MRI: cerebellar hypoplasia (HP:0001321). 1 1 Johan den Dunnen
00208533 - - - M - Germany - - - - - - - 1 1 Andreas Laner
00268052 TSEN54.ER PubMed: Sepahvand 2020 5-generation family, 2 affected brothers, unaffected heterozygous carrier parents/relatives M yes Iran - - - - - PCH - 1 2 Ehsan Razmara
00275971 CCM216 - - F - Romania - >02y09m - - - PCH - 1 1 Enza Maria Valente
00275972 CCM325 - - M - Italy - >18y09m - - - PCH - 1 1 Enza Maria Valente
00275973 CCM419 - - M - Italy - >01y03m - - - PCH - 1 1 Enza Maria Valente
00275974 CCM430 - - F - (Italy) - >00y09m - - - PCH - 1 1 Enza Maria Valente
00275975 CCM495 - - F - Italy - >04y - - - PCH - 1 1 Enza Maria Valente
00275976 CCM516 - - F - Italy - >00y04m - - - PCH - 1 1 Enza Maria Valente
00275977 CCM517 - - M - Italy - >02y - - - PCH - 1 1 Enza Maria Valente
00275978 CCM276 - - M - Italy - >04y06m - - - PCH - 1 1 Enza Maria Valente
00275979 CCM543 - - M - Italy - >00y04m - - - PCH - 1 1 Enza Maria Valente
00275980 CCM549 - - F - Italy - >01y - - - PCH - 1 1 Enza Maria Valente
00291843 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00291844 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 10 Mohammed Faruq
00301207 TSEN_54_Iranian - - M yes Iran Fars 02y? - no - PCH HP:0000252, HP:0007334, HP:0002353, HP:0001627, HP:0001272 1 1 Ehsan Razmara
00306766 - - - F - - - - - - - ? Abnormality of nervous system physiology (HP:0012638); Global developmental delay (HP:0001263); Aplasia/Hypoplasia of the cerebellum (HP:0007360); Hypoplasia of the pons (HP:0012110); Neurodevelopmental abnormality (HP:0012759) 1 1 Andreas Laner
00387705 M039 PubMed: Hu 2019 family, 2 affected individuals - - - Kurd - - - - ID syndromic intellectual disability, microcephaly, epilepsy 1 2 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.