Gene: KNL1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57082
Gene Symbol: KNL1
KNL1 		0.320 Biomarker disease BEFREE Absence of genetic interaction between casc5 and aspm or wdr62 further delineates centrosomal and non-centrosomal pathways in PM. 31696992 2019
Entrez Id: 57082
Gene Symbol: KNL1
KNL1 		0.320 Biomarker disease BEFREE Our findings substantiate the proposed role of CASC5 for primary microcephaly and suggest that it also might be relevant for genome stability. 26621532 2016
Entrez Id: 57082
Gene Symbol: KNL1
KNL1 		0.320 Biomarker disease GENOMICS_ENGLAND Kinetochore KMN network gene CASC5 mutated in primary microcephaly. 22983954 2012