All individuals with variants in gene SPTBN2

27 entries on 1 page. Showing entries 1 - 27.
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00001238 - - - F yes Egypt - - - - - SCA5 - 1 1 Hanno Bolz
00025013 - - - - no United States white - - - - SCAR14 severe bulbar, cerebellar, and proprioceptive dysfunction 2 1 Vikki Stefans
00143194 - - - F no Italy - - - - - SCA5 cerebellar atrophy, Cerebellar ataxia, Moderate global developmental delay, EEG abnormality, Dolichocephaly, Convergent strabismus, Infantile muscular hypotonia, Hyporeflexia of lower limbs 1 1 Enza Maria Valente
00154933 - - - F no Italy - - - - - SCA5 - 1 1 Enza Maria Valente
00275674 FamMCP119Pat1 PubMed: Santos-Cortez 2018 4-generation family, 2 affected (F, M), unaffected heterozygous carrier parents/relatives M yes Pakistan - - - - - ID OFC 47cm; IQ 30, severe intellectual disability (HP:0010864); microcephaly 1 2 Johan den Dunnen
00275675 FamMCP119Pat2 PubMed: Santos-Cortez 2018 - F yes Pakistan - - - - - ID OFC 45cm; IQ 30, severe intellectual disability (HP:0010864) 1 1 Johan den Dunnen
00290494 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 40 Mohammed Faruq
00290495 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 37 Mohammed Faruq
00290496 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00295588 - - - M - - - - - - - ? Ataxia (HP:0001251); Abnormality of the cerebellum (HP:0001317) 2 1 Andreas Laner
00296526 - - - F - - - - - - - ? Dysarthria (HP:0001260); Episodic ataxia (HP:0002131); Vertigo (HP:0002321) 1 1 Andreas Laner
00325410 Pat23 PubMed: Hong 2020 - M - Taiwan - - - - - ? no seizures; frequent ataxia 1 1 Johan den Dunnen
00362271 142871 - - M ? Germany - - - - - SCA5 (+) Seizure,(+) Ataxia,(+) Spastic tetraparesis,(+) Dysmetria,(+) EEG abnormality,(+) Spastic dysarthria,(+) Intellectual disability, progressive,(+) Abnormal visual electrophysiology 1 1 Andreas Laner
00374866 S-5649 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00397435 189082 - - M no Germany - - - - - SCA5 Ataxia, Abnormality of coordination, Gait ataxia, Impaired distal vibration sensation, Hyperreflexia, Cerebellar atrophy, Progressive cerebellar ataxia 1 1 Andreas Laner
00405008 - - - M yes Egypt - - - - - SCA5 27-y male The patient presents with abnormality of movement, ataxia, fasciculations, muscle weakness, muscular hypotonia, peripheral neuropathy, skeletal muscle atrophy and tremor. 1 1 Sherifa Ahmed Hamed
00408676 Pat39 PubMed: Thomas 2022 no family history - no France - - - - - ? - 1 1 Johan den Dunnen
00435089 - - - M yes Egypt - - - - - SCA5 - 1 1 Sherifa Ahmed Hamed
00448202 Pat62 PubMed: Poli 2024 - F - Chile - - - - - ? global developmental delay; microcephaly; cerebellar atrophy; gait ataxia 1 1 Johan den Dunnen
00455772 Pat12 PubMed: Salinas 2020 patient F - - - - - - - ? - 1 1 Johan den Dunnen
00455868 Pat108 PubMed: Salinas 2020 patient M - - - - - - - ? - 1 1 Johan den Dunnen
00455981 - - - - - ? (unknown) - - - - - SCA - 1 1 Min Peng
00468001 Pat4 PubMed: Schnekenberg 2015 2-generation family, 1 affected, unaffected non-carrier parents F no Italy - - - - - ataxia see paper; ..., birth at term, 1 previous miscarriages; ataxia, intellectual disability; no clinical regression; moderate intellectual disability; MRI brain mild cerebellar hypoplasia/atrophy 1 1 Johan den Dunnen
00469420 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
00469421 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
00470619 Pat248 PubMed: Wai 2020 studied effect of variant on RNA - - United Kingdom (Great Britain) - - - - - ? - 1 1 Johan den Dunnen
00471048 family PubMed: Canault 2014 4-generation family, 3 affected (sister/2 brothers) , unaffected heterozygous carrier parents/relatives F;M yes France - - - - - BDPLT see paper; ..., 18m-mucocutaneous bleeding, prolonged evere epistaxis, hematomas, bleeding after tooth extraction; female massive menorrhagia, chronic anemia 1 3 Johan den Dunnen
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