Kearns-Sayre Syndrome

A rare mitochondrial myopathy characterized by a progressive limitation of eye movements, leading to immobility and eye drop. It may be associated with muscle weakness, heart block, hearing loss, ataxia and short stature. (NCI Thesaurus)

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KEAP1 wt Allele

Human KEAP1 wild-type allele is located in the vicinity of 19p13.2 and is approximately 18 kb in length. This allele, which encodes…

KEAP1 Gene

This gene is involved in ubiquitin-mediated protein degradation.

KDSR wt Allele

Human FVT1 wild-type allele is located in the vicinity of 18q21.3 and is approximately 37 kb in length. This allele, which encodes…

KDSR Gene

This gene plays a role in glycosphingolipid metabolism.

KDR wt Allele

Human KDR wild-type allele is located within 4q11-q12 and is approximately 47 kb in length. This allele, which encodes vascular endothelial growth…

KDR Gene

This gene plays a role in angiogenesis and vascular regulation.