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Browse result for Cerebellar ataxia

※ introduction

    Cerebellar ataxia is a form of ataxia originating in the cerebellum. Non-progressive congenital ataxia (NPCA) is a classical presentation of cerebral ataxias. Cerebellar ataxia can occur as a result of many diseases and may present with symptoms of an inability to coordinate balance, gait, extremity and eye movements. Lesions to the cerebellum can cause dyssynergia, dysmetria, dysdiadochokinesia, dysarthria and ataxia of stance and gait. Deficits are observed with movements on the same side of the body as the lesion (ipsilateral). Clinicians often use visual observation of people performing motor tasks in order to look for signs of ataxia.

Reference
Wiki: Cerebellar ataxia



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00376P263581786
DNMT1
DNA -methyltransferase 1
Homo sapiens
PTMD01484P071964747
NEFL
Neurofilament light polypeptide
Homo sapiens
PTMD01106P542536310
ATXN1
Ataxin-1
Homo sapiens
PTMD01120Q04656538
ATP7A
Copper-transporting ATPase 1
Homo sapiens
PTMD02482O150206712
SPTBN2
Spectrin beta chain, non-erythrocytic 2
Homo sapiens
PTMD04150P13637478
ATP1A3
Sodium/potassium-transporting ATPase subunit alpha-3 /K ATPase alpha-3 subunit) /K ATPase alpha subunit)
Homo sapiens
PTMD04705P283314719
NDUFS1
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial
Homo sapiens
PTMD04904P35219767
CA8
Carbonic anhydrase-related protein
Homo sapiens
PTMD05245P485062729
GCLC
Glutamate--cysteine ligase catalytic subunit
Homo sapiens
PTMD08857Q7Z5J410743
RAI1
Retinoic acid-induced protein 1
Homo sapiens
PTMD11367Q96J0283737
ITCH
E3 ubiquitin-protein ligase Itchy homolog
Homo sapiens
PTMD12949Q9H8M554805
CNNM2
Metal transporter CNNM2
Homo sapiens
PTMD13461Q9NTI251761
ATP8A2
Phospholipid-transporting ATPase IB
Homo sapiens
PTMD13975Q9UBB425814
ATXN10
Ataxin-10
Homo sapiens