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Browse result for Encephalopathy

※ introduction

    Encephalopathy (; from Ancient Greek: ?¦Ã�¦Ê?¦Õ¦Ã�¦Ë¦Ã�? "brain" + ¦Ã�?¦È¦Ã�? "suffering") means any disorder or disease of the brain, especially chronic degenerative conditions. In modern usage, encephalopathy does not refer to a single disease, but rather to a syndrome of overall brain dysfunction; this syndrome has many possible organic and inorganic causes.

Reference
Wiki: Encephalopathy



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00450O0042910059
DNM1L
Dynamin-1-like protein
Homo sapiens
PTMD00670Q131147187
TRAF3
TNF receptor-associated factor 3
Homo sapiens
PTMD00211Q9UHD229110
TBK1
Serine/threonine-protein kinase TBK1
Homo sapiens
PTMD00836Q9Y2G1745
MYRF
Myelin regulatory factor [Cleaved into: Myelin regulatory factor, N-terminal; Myelin regulatory factor, C-terminal]
Homo sapiens
PTMD01650P516084204
MECP2
Methyl-CpG-binding protein 2
Homo sapiens
PTMD04950P356588021
NUP214
Nuclear pore complex protein Nup214
Homo sapiens
PTMD05006P38606523
ATP6V1A
V-type proton ATPase catalytic subunit A
Homo sapiens
PTMD05203P478702561
GABRB2
Gamma-aminobutyric acid receptor subunit beta-2 receptor subunit beta-2)
Homo sapiens
PTMD05345P497925903
RANBP2
E3 SUMO-protein ligase RanBP2
Homo sapiens
PTMD09300Q8IW4555739
NAXD
ATP-dependent -NADH-hydrate dehydratase HX dehydratase) HX dehydratase)
Homo sapiens
PTMD11834Q995745274
SERPINI1
Neuroserpin
Homo sapiens
PTMD12118Q9BTW96904
TBCD
Tubulin-specific chaperone D
Homo sapiens
PTMD00882O3530311411
Dnm1l
Dynamin-1-like protein
Rattus norvegicus