Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9276
Gene Symbol: COPB2
COPB2
Autosomal Recessive Primary Microcephaly
0.300 GermlineCausalMutation ORPHANET Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly. 29036432

2017