Microcephaly Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_10907)
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Genes

35 genes involed in the disease Microcephaly from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
ZNF335 zinc finger protein 335 4.0
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila) 4.0
CDK5RAP2 CDK5 regulatory subunit associated protein 2 4.0
MFSD2A major facilitator superfamily domain containing 2A 4.0
CTU2 cytosolic thiouridylase subunit 2 homolog (S. pombe) 4.0
CDK6 cyclin-dependent kinase 6 4.0
STIL SCL/TAL1 interrupting locus 4.0
CEP135 centrosomal protein 135kDa 4.0
NCAPD2 non-SMC condensin I complex, subunit D2 4.0
NCAPD3 non-SMC condensin II complex, subunit D3 4.0
PDCD6IP programmed cell death 6 interacting protein 4.0
WDR62 WD repeat domain 62 4.0
NUP37 nucleoporin 37kDa 4.0
TUBGCP4 tubulin, gamma complex associated protein 4 4.0
QARS1 glutaminyl-tRNA synthetase 1 4.0
PRUNE1 prune exopolyphosphatase 1 4.0
CEP152 centrosomal protein 152kDa 4.0
PNKP polynucleotide kinase 3'-phosphatase 4.0
CIT citron rho-interacting serine/threonine kinase 4.0
PCDH12 protocadherin 12 4.0
BUB1 BUB1 mitotic checkpoint serine/threonine kinase 4.0
RRP7A ribosomal RNA processing 7 homolog A (S. cerevisiae) 4.0
ANKLE2 ankyrin repeat and LEM domain containing 2 4.0
PHC1 polyhomeotic homolog 1 (Drosophila) 4.0
LMNB2 lamin B2 4.0
LMNB1 lamin B1 4.0
WDFY3 WD repeat and FYVE domain containing 3 4.0
NCAPH non-SMC condensin I complex, subunit H 4.0
SASS6 spindle assembly 6 homolog (C. elegans) 4.0
KIF14 kinesin family member 14 4.0
COPB2 coatomer protein complex, subunit beta 2 (beta prime) 4.0
TCF4 transcription factor 4 4.0
CENPE centromere protein E, 312kDa 4.0
MCPH1 microcephalin 1 4.0
KNL1 kinetochore scaffold 1 4.0