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Browse result for Abnormality of neuronal migration

※ introduction

    Neuronal migration disorder (NMD) refers to a heterogenous group of disorders that, it is supposed, share the same etiopathological mechanism: a variable degree of disruption in the migration of neuroblasts during neurogenesis. The neuronal migration disorders are termed cerebral dysgenesis disorders, brain malformations caused by primary alterations during neurogenesis; on the other hand, brain malformations are highly diverse and refer to any insult to the brain during its formation and maturation due to intrinsic or extrinsic causes that ultimately will alter the normal brain anatomy. However, there is some controversy in the terminology because virtually any malformation will involve neuroblast migration, either primarily or secondarily.

Reference
Wiki: Abnormality of neuronal migration



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01276Q8WXI794025
MUC16
Mucin-16
Homo sapiens
PTMD02582O154008417
STX7
Syntaxin-7
Homo sapiens
PTMD02683O4337928440
WDR62
WD repeat-containing protein 62
Homo sapiens
PTMD06708Q142041778
DYNC1H1
Cytoplasmic dynein 1 heavy chain 1
Homo sapiens
PTMD06792Q1467823189
KANK1
KN motif and ankyrin repeat domain-containing protein 1
Homo sapiens
PTMD07332Q3MII64943
TBC1D25
TBC1 domain family member 25
Homo sapiens
PTMD07596Q5JRC915872
FAM47A
Protein FAM47A
Homo sapiens
PTMD09269Q8IVF211314
AHNAK2
Protein AHNAK2
Homo sapiens
PTMD10338Q8TCG255300
PI4K2B
Phosphatidylinositol 4-kinase type 2-beta
Homo sapiens
PTMD10814Q928172125
EVPL
Envoplakin
Homo sapiens
PTMD10948Q969Y091775
NXPE3
NXPE family member 3
Homo sapiens
PTMD12907Q9H7P964857
PLEKHG2
Pleckstrin homology domain-containing family G member 2
Homo sapiens
PTMD13393Q9NRR429102
DROSHA
Ribonuclease 3
Homo sapiens
PTMD14013Q9UBP64234
METTL1
tRNA -)-methyltransferase -)-methyltransferase) -)-methyltransferase) -N)-methyltransferase) -methyltransferase)
Homo sapiens