All individuals with variants in gene DARS

13 entries on 1 page. Showing entries 1 - 13.
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00011647 - - 2-generation family, father of 00016304, healthy parents and brother do not carry de novo variant; performed exome/genome analysis, detected possibly causative variant but have not yet sufficient evidence to publish - please contact me M no Netherlands - - 1 - - CMT2, HYDRO peripheral neuropathy (demyelinating motor sensory neuropathy ), dysmorphic facial features , hypospadias, craniosynostosis, minor insufficiency of the aortic valve, mild glaucoma, mild learning disabilities 1 2 Thomas Potjer
00016218 - PubMed: Taft 2013 2-generation family, unaffected carrier parents M no Australia - - - - - HBSL see paper 2 3 Johan den Dunnen
00016219 - PubMed: Taft 2013 2-generation family, affecteds sibs, unaffected carrier parents M yes India;Pakistan - - - - - HBSL see paper 1 4 Johan den Dunnen
00016220 - PubMed: Taft 2013 2-generation family, patient and unaffected carrier parents M yes India - - - - - HBSL see paper 1 3 Johan den Dunnen
00016221 - PubMed: Taft 2013 2-generation family, patient and unaffected carrier parents M yes India;Pakistan - - - - - HBSL see paper 1 3 Johan den Dunnen
00016222 - PubMed: Taft 2013 2-generation family, 2 affected sibs and unaffected carrier parents F no United States - - - - - HBSL see paper 2 4 Johan den Dunnen
00016223 - PubMed: Taft 2013 2-generation family, patient and unaffected carrier parents M yes India;Pakistan - - - - - HBSL see paper 1 3 Johan den Dunnen
00016225 - PubMed: Taft 2013 2-generation family, affected brother/sister and unaffected carrier parents - no United Kingdom (Great Britain) - - - - - HBSL see paper 2 4 Johan den Dunnen
00016304 - - 2-generation family, son of 00011647 M no Netherlands - - - - - HYDRO - 1 1 Thomas Potjer
00081061 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - HBSL Hypomyelination with brainstem and spinal cord involvement and leg spasticity (OMIM:615281) 1 1 Daniel Trujillano
00150173 26539891-FamBAB3404 PubMed: Karaca 2015 - - - - - - - family structure in paper - ? microcephaly, strabismus, 1 1 Johan den Dunnen
00246631 - - - ? - - - - - - - - HP:0010952 (Mild fetal ventriculomegaly); HP:0001331 (Absent septum pellucidum); HP:0002119 (Ventriculomegaly); HP:0001197 (Abnormality of prenatal development or birth) 1 1 Andreas Laner
00292249 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
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