Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57082
Gene Symbol: KNL1
KNL1
CUI: C1858516
Disease: MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE 		0.700 Biomarker GENOMICS_ENGLAND Refining the phenotype associated with CASC5 mutation. 26626498

2016
Entrez Id: 57082
Gene Symbol: KNL1
KNL1
CUI: C1858516
Disease: MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE 		0.700 Biomarker GENOMICS_ENGLAND Kinetochore KMN network gene CASC5 mutated in primary microcephaly. 22983954

2012