VRK1 Chromosome 14

VRK serine/threonine kinase 1
84 variants 84 Health Risk

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What This Gene Does
This gene encodes a member of the vaccinia-related kinase (VRK) family of serine/threonine protein kinases. This gene is widely expressed in human tissues and has increased expression in actively dividing cells, such as those in testis, thymus, fetal liver, and carcinomas. Its protein localizes to the nucleus and has been shown to promote the stability and nuclear accumulation of a transcriptionally active p53 molecule and, in vitro, to phosphorylate Thr18 of p53 and reduce p53 ubiquitination. This gene, therefore, may regulate cell proliferation. This protein also phosphorylates histone, casein, and the transcription factors ATF2 (activating transcription factor 2) and c-JUN. [provided by RefSeq, Jul 2008]
Associated Conditions (19)
Distal hereditary motor neuropathy associated with upper motor neuron signs
Distal spinal muscular atrophy
Neuronopathy
distal hereditary motor
autosomal recessive 10
Pontocerebellar hypoplasia type 1A
Congenital pontocerebellar hypoplasia type 1
Inborn genetic diseases
VRK1-related disorder
Amyotrophic lateral sclerosis
autosomal recessive
Spinal muscular atrophy
Hereditary breast ovarian cancer syndrome
Microcephaly-complex motor and sensory axonal neuropathy syndrome
EMG: neuropathic changes
Pontocerebellar hypoplasia type 1B
Pontoneocerebellar hypoplasia
Abnormality of the musculature
Juvenile amyotrophic lateral sclerosis
Key Variants
RS1172497555
Conflicting classifications of pathogenicity
Distal hereditary motor neuropathy associated with upper motor neuron signs, Distal spinal muscular atrophy, Neuronopathy
Health Risk
RS1334577291
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
Health Risk
RS139476915
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 1A, Congenital pontocerebellar hypoplasia type 1, Distal spinal muscular atrophy
Health Risk
RS146113610
Conflicting classifications of pathogenicity
Hereditary breast ovarian cancer syndrome, Pontocerebellar hypoplasia type 1A, Inborn genetic diseases
Health Risk
RS147853760
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 1A, Inborn genetic diseases, Pontocerebellar hypoplasia type 1A
Health Risk
RS1595676477
Conflicting classifications of pathogenicity
Microcephaly-complex motor and sensory axonal neuropathy syndrome, EMG: neuropathic changes, Pontocerebellar hypoplasia type 1A
Health Risk
RS1595676517
Conflicting classifications of pathogenicity
Distal hereditary motor neuropathy associated with upper motor neuron signs, Distal spinal muscular atrophy, Neuronopathy
Health Risk
RS2230532
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
Health Risk
RS375176918
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
Health Risk
RS387906830
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 1A, Neuronopathy, distal hereditary motor
Health Risk
RS541660707
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 1A, Congenital pontocerebellar hypoplasia type 1, Inborn genetic diseases
Health Risk
RS61736727
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 1A, Inborn genetic diseases, Pontocerebellar hypoplasia type 1A
Health Risk
All Variants (84)
RSID Category Clinical Significance Conditions
RS1172497555 Health Risk Conflicting classifications of pathogenicity Distal hereditary motor neuropathy associated with upper motor neuron signs, Distal spinal muscular atrophy, Neuronopathy
RS1334577291 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS139476915 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Congenital pontocerebellar hypoplasia type 1, Distal spinal muscular atrophy
RS146113610 Health Risk Conflicting classifications of pathogenicity Hereditary breast ovarian cancer syndrome, Pontocerebellar hypoplasia type 1A, Inborn genetic diseases
RS147853760 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Inborn genetic diseases, Pontocerebellar hypoplasia type 1A
RS1595676477 Health Risk Conflicting classifications of pathogenicity Microcephaly-complex motor and sensory axonal neuropathy syndrome, EMG: neuropathic changes, Pontocerebellar hypoplasia type 1A
RS1595676517 Health Risk Conflicting classifications of pathogenicity Distal hereditary motor neuropathy associated with upper motor neuron signs, Distal spinal muscular atrophy, Neuronopathy
RS2230532 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS375176918 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS387906830 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Neuronopathy, distal hereditary motor
RS541660707 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Congenital pontocerebellar hypoplasia type 1, Inborn genetic diseases
RS61736727 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Inborn genetic diseases, Pontocerebellar hypoplasia type 1A
RS767585930 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Congenital pontocerebellar hypoplasia type 1, Pontocerebellar hypoplasia type 1A
RS771364038 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Neuronopathy, distal hereditary motor
RS780789145 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 1A, Neuronopathy, distal hereditary motor
RS794727029 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Pontocerebellar hypoplasia type 1A, Inborn genetic diseases
RS1482696609 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A, Inborn genetic diseases
RS1566696845 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1B, Pontocerebellar hypoplasia type 1B
RS1887280587 Health Risk Likely pathogenic Distal spinal muscular atrophy, Distal spinal muscular atrophy
RS1888018806 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139749072 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139804166 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139845854 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Neuronopathy, distal hereditary motor
RS2139845924 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2504141901 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2504169004 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2504169446 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2504184408 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2504194332 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2504194954 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2504251871 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS773138218 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Inborn genetic diseases, Neuronopathy
RS774518440 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 1A, Inborn genetic diseases, Pontocerebellar hypoplasia type 1A
RS1174255706 Health Risk Pathogenic Pontoneocerebellar hypoplasia, Pontoneocerebellar hypoplasia
RS1200170208 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS1257821102 Health Risk Pathogenic Inborn genetic diseases, Pontocerebellar hypoplasia type 1A, Inborn genetic diseases
RS1298866730 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS137853063 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Inborn genetic diseases, Congenital pontocerebellar hypoplasia type 1
RS1566713184 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS1887100431 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS1887100980 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS1889019962 Health Risk Pathogenic Spinal muscular atrophy, Pontocerebellar hypoplasia type 1A, Spinal muscular atrophy
RS2139748811 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139748841 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139759363 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Inborn genetic diseases, Pontocerebellar hypoplasia type 1A
RS2139795550 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139796429 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139801958 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139804073 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
RS2139814687 Health Risk Pathogenic Pontocerebellar hypoplasia type 1A, Pontocerebellar hypoplasia type 1A
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