Abstract
VRK1 is a novel human putative serine/threonine kinase, and is located on chromosome 14 at band q32 where an autosomal recessive congenital microphthalmia (CMIC) is mapped. We isolated a polymorphic dinucleotide CA repeat marker from a genomic clone containing the human VRK1 gene. This polymorphism will be useful in genetic studies of disorders localized at the 14q32 region, such as CMIC.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Base Sequence
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Chromosome Mapping
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Chromosomes, Human, Pair 14
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DNA Primers
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Dinucleotide Repeats*
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Eye Abnormalities / genetics
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Humans
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Intracellular Signaling Peptides and Proteins
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Polymerase Chain Reaction
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Polymorphism, Genetic*
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Protein Serine-Threonine Kinases / genetics*
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Proteins*
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Viral Proteins / genetics*
Substances
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DNA Primers
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Intracellular Signaling Peptides and Proteins
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Proteins
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Viral Proteins
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Protein Serine-Threonine Kinases
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VRK1 protein, human