All individuals with variants in gene BSND

46 entries on 1 page. Showing entries 1 - 46.
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     
00281824 F314 PubMed: Birkenhäger 2001 family - yes Turkey - - - - - ? sensorineural deafness, kidney failure 1 1 Global Variome, with Curator vacancy
00281825 - PubMed: Ozlu 2006 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00281826 F662 PubMed: Birkenhäger 2001 family - no United Kingdom (Great Britain) - - - - - ? sensorineural deafness, kidney failure 2 1 Global Variome, with Curator vacancy
00281827 PKDF815 PubMed: Riazuddin 2009 6-generation family, 27 affected (13F, 14M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - ? see paper; ... 1 24 Johan den Dunnen
00281828 F813 PubMed: Birkenhäger 2001 - - yes - North Africa - - - - ? sensorineural deafness, kidney failure 1 1 Global Variome, with Curator vacancy
00281829 F206 PubMed: Birkenhäger 2001 family - yes France - - - - - ? sensorineural deafness, kidney failure 1 1 Global Variome, with Curator vacancy
00281830 - PubMed: Brennan 1998, PubMed: Birkenhäger 2001 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00281831 PKDF393 PubMed: Riazuddin 2009 5-generation family, 4 affected (2F, 2M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - deafness see paper; ... 1 4 Global Variome, with Curator vacancy
00281832 - PubMed: Kitanaka 2006 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00281833 - PubMed: Shafique 2014 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00281834 - PubMed: Estévez 2001 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00281835 - PubMed: Zaffanello 2006 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00281836 - PubMed: Duzkale 2013 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00281837 - PubMed: Ozlu 2006, PubMed: Xiong 2015 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00281838 - PubMed: Gulsuner 2013 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00281839 - PubMed: de Pablos 2014 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00281840 - PubMed: Duzkale 2013 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00281841 - PubMed: Duzkale 2013 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00281842 - PubMed: Duzkale 2013 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00281843 - PubMed: Duzkale 2013 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00320324 PT940 - - - - Japan Asian - - - - BARTS4A - 1 1 Takayasu Mori
00320384 F591 PubMed: Birkenhäger 2001 family - yes Turkey - - - - - ? sensorineural deafness, kidney failure 1 1 Johan den Dunnen
00320385 F730 PubMed: Birkenhäger 2001 family - yes Turkey - - - - - ? sensorineural deafness, kidney failure 1 1 Johan den Dunnen
00320387 F786 PubMed: Birkenhäger 2001 family - yes Turkey - - - - - ? sensorineural deafness, kidney failure 1 1 Johan den Dunnen
00320388 F791 PubMed: Birkenhäger 2001 family - yes Turkey - - - - - ? sensorineural deafness, kidney failure 1 1 Johan den Dunnen
00320395 F542 PubMed: Birkenhäger 2001 family - yes Israel - - - - - ? sensorineural deafness, kidney failure 1 1 Johan den Dunnen
00320397 F197 PubMed: Birkenhäger 2001 family - yes - North Africa - - - - ? sensorineural deafness, kidney failure 1 1 Johan den Dunnen
00320398 F708 PubMed: Birkenhäger 2001 family - yes Lebanon - - - - - ? sensorineural deafness, kidney failure 1 1 Johan den Dunnen
00320404 patient PubMed: Miyamura 2003 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Japan - - - - - ? congenital sensorineural deafness, mild Bartter syndrome 1 1 Johan den Dunnen
00320412 PKDF606;HLAI-23 PubMed: Riazuddin 2009, PubMed: Naz 2017 4-generation family, 5 affected (2F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - deafness see paper; ... 1 5 Johan den Dunnen
00320415 PKDF067 PubMed: Riazuddin 2009 5-generation family, 4 affected (3F, M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - deafness see paper; ... 1 4 Johan den Dunnen
00320419 PKDF815 PubMed: Riazuddin 2009 3 affected (2F, M), separate branch family F;M yes Pakistan - - - - - ? see paper; ... 2 3 Johan den Dunnen
00361960 Pat34 PubMed: Brochard 2009 patient - - France white - - - - BARTS - 1 1 Johan den Dunnen
00361961 Pat35 PubMed: Brochard 2009 patient - - France white - - - - BARTS - 1 1 Johan den Dunnen
00361962 Pat36 PubMed: Brochard 2009 patient - - Algeria - - - - - BARTS - 1 1 Johan den Dunnen
00361963 Pat37 PubMed: Brochard 2009 patient - - France white - - - - BARTS - 1 1 Johan den Dunnen
00441140 DEM4304 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441141 DEM4384 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441142 DEM4558 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441143 DEM4150 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441144 DEM4576 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441145 DEM4592 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441146 DEM4593 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441147 PKDF970b PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441148 PKDF1673 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441149 PKSR20 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 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.