All individuals with variants in gene SPATA5

23 entries on 1 page. Showing entries 1 - 23.
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00049849 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 2 affected sisters; unaffected heterozygous carrier parents F no - European >06y - - - ? see paper; hypotonia, spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI thin corpus callosum, no seizures, EEG abnormal, gastrointestinal issues , ... 2 2 Johan den Dunnen
00049850 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, afffected brother/sister, unaffected heterozygous carrier parents M no - Hispanic >11y - - - ? see paper; hypotonia, spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI progressive diffuse atrophy, seizures, EEG abnormal, gastrointestinal issues , ... 2 2 Johan den Dunnen
00049851 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 2 affected sisters; unaffected heterozygous carrier parents F no - European >09y - - - ? see paper; hypotonia, spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI thin corpus callosum, seizures, EEG abnormal, gastrointestinal issues, … 2 1 Johan den Dunnen
00049852 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, afffected brother/sister, unaffected heterozygous carrier parents F no - Hispanic >06y - - - ? see paper; hypotonia, no spasticity, developmental delay, vision defect?, sensorineural hearing loss, microcephaly, MRI normal, seizures, EEG abnormal, gastrointestinal issues, … 2 1 Johan den Dunnen
00049853 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 1 afffected, unaffected heterozygous carrier parents F no - European >5y - - - ? see paper; hypotonia, spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI delayed myelination, seizures, EEG abnormal, gastrointestinal issues, … 2 1 Johan den Dunnen
00049854 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 1 afffected, unaffected heterozygous carrier parents F no - European >4y - - - ? see paper; hypotonia, no spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI normal, seizures, EEG abnormal, gastrointestinal issues, … 2 1 Johan den Dunnen
00049855 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 1 afffected, unaffected heterozygous carrier parents F no - European >2y - - - ? see paper; hypotonia, spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI hypomyelination, seizures, EEG abnormal, gastrointestinal issues, … 2 1 Johan den Dunnen
00049856 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, afffected brother/sister, unaffected heterozygous carrier parents M no - European >19y - - - ? see paper; hypotonia, spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly?, MRI cortical atrophy, immature myelination, seizures, EEG abnormal, gastrointestinal issues , ... 2 2 Johan den Dunnen
00049857 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 2 afffected brothers, unaffected heterozygous carrier parents M no - European >8y - - - ? see paper; hypertonia, spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI normal, seizures, EEG abnormal, gastrointestinal issues, ... 2 2 Johan den Dunnen
00049858 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 1 afffected, unaffected heterozygous carrier parents M no - European >5y - - - ? see paper; hypotonia, spasticity, developmental delay, vision defect, sensorineural hearing loss, no microcephaly, MRI enlarged cerebrospinal fluid spaces, seizures, EEG abnormal, gastrointestinal issues, … 2 1 Johan den Dunnen
00049859 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 1 afffected, unaffected heterozygous carrier parents F - - European >11y - - - ? see paper; hypotonia, no spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI enlarged cerebrospinal fluid spaces, seizures, EEG abnormal, gastrointestinal issues, … 1 1 Johan den Dunnen
00049860 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 1 afffected, unaffected heterozygous carrier parents M - - European >4y - - - ? see paper; hypotonia, no spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, MRI normal, seizures, EEG abnormal, gastrointestinal issues, … 1 1 Johan den Dunnen
00049863 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, afffected brother/sister, unaffected heterozygous carrier parents F no - European >19y - - - ? see paper; hypotonia, no spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, no MRI, seizures, EEG abnormal, no gastrointestinal issues, … 2 1 Johan den Dunnen
00049864 - PubMed: Tanaka 2015, Journal: Tanaka 2015 2-generation family, 2 afffected brothers, unaffected heterozygous carrier parents M no - European >8y - - - ? see paper; hypotonia, no spasticity, developmental delay, vision defect, sensorineural hearing loss, microcephaly, no MRI, seizures, EEG abnormal, gastrointestinal issues, … 2 1 Johan den Dunnen
00103212 - PubMed: Puusepp 2018, Journal: Puusepp 2018 see paper, 2 sibs, same phenotype - - Estonia - - - - - ? see paper, 2 sibs, epilepsy, hearing loss, developmental delay, early death 2 2 Sander Pajusalu
00103213 - PubMed: Puusepp 2018, Journal: Puusepp 2018 see paper, Patient 3 F - Estonia - - - - - ? see paper, epilepsy, hearing loss, developmental delay 2 1 Sander Pajusalu
00103214 - PubMed: Puusepp 2018, Journal: Puusepp 2018 see paper, Patient 4 M - Estonia - - - - - ? see paper, epilepsy, hearing loss, developmental delay 2 1 Sander Pajusalu
00103215 - PubMed: Puusepp 2018, Journal: Puusepp 2018 see paper, Patient 5 F - Estonia - - - - - ? see paper, epilepsy, hearing loss, developmental delay 2 1 Sander Pajusalu
00177015 47651 - - M no Switzerland - - - - - EE HP:0000666 HP:0002451 HP:0001285 1 1 Anaïs Begemann
00177016 73068 - - M no Switzerland - - - - - EE HP:0000407 HP:0001285 HP:0012043 HP:0000565 HP:0002015 HP:0000276 HP:0000275 HP:0000286 HP:0000431 HP:0002705 HP:0012098 HP:0005257 HP:0000953 2 1 Anaïs Begemann
00207920 - - - M - Germany - - - - - - HP:0002133 (Status epilepticus) 1 1 Andreas Laner
00293535 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00404729 192779 - - F no Germany - - - - - EHLMRS Hearing Hypsarrhythmia, impairment, Global developmental delay, Seizure 2 1 Andreas Laner
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