Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9918
Gene Symbol: NCAPD2
NCAPD2
CUI: C4693831
Disease: MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE 		0.300 GeneticVariation UNIPROT Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders. 28097321

2017
Entrez Id: 9918
Gene Symbol: NCAPD2
NCAPD2
CUI: C4693831
Disease: MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE 		0.300 GeneticVariation UNIPROT Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis. 27737959

2016