All individuals with variants in gene PRKCG

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00073123 - ATX425 - M - France - - - - - SCA14 - 1 1 Claire Guissart
00073124 - ATX535 - M - France - - - - - SCA14 - 1 1 Claire Guissart
00106553 606181126 - Mother is also affected F ? (Germany) - - - no - SCA1, SCA10, SCA11, SCA14, SCA17, SCA27A, SCA5, SCA6, SCA7, SCA8 - 1 1 Friederike Hein
00248423 - - - F - - - - - - - - HP:0012759 (Neurodevelopmental abnormality); HP:0011458 (Abdominal symptom); HP:0002013 (Vomiting); HP:0002066 (Gait ataxia); HP:0100022 (Abnormality of movement); HP:0001627 (Abnormality of cardiac morphology); HP:0001637 (Abnormality of the myocardium); HP:0012547 (Abnormal involuntary eye movements); HP:0001263 (Global developmental delay); HP:0000666 (Horizontal nystagmus) 1 1 Andreas Laner
00292194 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00390050 187548 - - M no Germany - - - - - SCA14 Ataxia, Cerebellar atrophy, Spastic paraplegia, Optic neuropathy, Dysarthria, Difficulty in tongue movements, Hyperreflexia; Son (untested) with similar symptoms 1 1 Andreas Laner
00408703 Pat29 PubMed: Thomas 2022 patient and affected brother - - France - - - - - ? - 1 1 Johan den Dunnen
00409979 - - - - - - - - - - - ataxia - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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