Severe Congenital Microcephaly Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C3853041
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Genes

34 genes associated with the disease Severe Congenital Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AP4M1 adaptor-related protein complex 4, mu 1 subunit
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
CEP63 centrosomal protein 63kDa
CLPB ClpB homolog, mitochondrial AAA ATPase chaperonin
DNM1L dynamin 1-like
DNMT3A DNA (cytosine-5-)-methyltransferase 3 alpha
DONSON downstream neighbor of SON
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
ERCC6 excision repair cross-complementation group 6
FOXG1 forkhead box G1
HIST1H4C histone cluster 1, H4c
KIF2A kinesin heavy chain member 2A
KIF5C kinesin family member 5C
KIFBP kinesin family binding protein
MFSD2A major facilitator superfamily domain containing 2A
NDE1 nudE neurodevelopment protein 1
ORC1 origin recognition complex, subunit 1
PHGDH phosphoglycerate dehydrogenase
PLK4 polo-like kinase 4
PNKP polynucleotide kinase 3'-phosphatase
PQBP1 polyglutamine binding protein 1
SIN3A SIN3 transcription regulator family member A
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
STAMBP STAM binding protein
TBCD tubulin folding cofactor D
TCF4 transcription factor 4
TRAIP TRAF interacting protein
TSEN2 TSEN2 tRNA splicing endonuclease subunit
TSEN34 TSEN34 tRNA splicing endonuclease subunit
TSEN54 TSEN54 tRNA splicing endonuclease subunit
TUBG1 tubulin, gamma 1
WDR62 WD repeat domain 62
ZC4H2 zinc finger, C4H2 domain containing