Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55605
Gene Symbol: KIF21A
KIF21A
0.220 Biomarker disease MGD Human CFEOM1 mutations attenuate KIF21A autoinhibition and cause oculomotor axon stalling. 24656932 2014
Entrez Id: 55605
Gene Symbol: KIF21A
KIF21A
0.220 GeneticVariation disease BEFREE We now identify additional pedigrees with CFEOM1 to determine if the disorder is genetically heterogeneous and, if so, if any affected members of CFEOM1 pedigrees or sporadic cases of classic CFEOM harbor mutations in ARIX, the CFEOM2 disease gene. 11882252 2002
Entrez Id: 55605
Gene Symbol: KIF21A
KIF21A
0.220 GeneticVariation disease BEFREE Here, we describe the phenotypic findings in a similarly affected Yemenite family and analyze the family for linkage to the CFEOM2 locus, as well as to the autosomal dominant CFEOM1 and CFEOM3 loci on chromosomes 12cen and 16q24, respectively. 10844060 2000