GNE Chromosome 9

Glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
243 variants 243 Health Risk

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What This Gene Does
The protein encoded by this gene is a bifunctional enzyme that initiates and regulates the biosynthesis of N-acetylneuraminic acid (NeuAc), a precursor of sialic acids. It is a rate-limiting enzyme in the sialic acid biosynthetic pathway. Sialic acid modification of cell surface molecules is crucial for their function in many biologic processes, including cell adhesion and signal transduction. Differential sialylation of cell surface molecules is also implicated in the tumorigenicity and metastatic behavior of malignant cells. Mutations in this gene are associated with sialuria, autosomal recessive inclusion body myopathy, and Nonaka myopathy. Alternative splicing of this gene results in transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Associated Conditions (12)
Sialuria
GNE myopathy
GNE-related disorder
Thrombocytopenia 12 with or without myopathy
Inborn genetic diseases
Malignant tumor of urinary bladder
Thrombocytopenia
Lung cancer
Hereditary nonpolyposis colon cancer
Myopathy
autophagic vacuolar
infantile-onset
Key Variants
All Variants (243)
RSID Category Clinical Significance Conditions
RS756488394 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, Inborn genetic diseases
RS758086020 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, GNE-related disorder
RS759945787 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS760509369 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, GNE-related disorder
RS762009737 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS763368889 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Sialuria
RS766266918 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Malignant tumor of urinary bladder
RS766818430 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Inborn genetic diseases
RS768321445 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS772597073 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS774849278 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Sialuria
RS776582567 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Sialuria
RS777310871 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Sialuria
RS781586600 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS794727279 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS794727505 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Thrombocytopenia, Sialuria
RS886043636 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS886043979 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS886044498 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Sialuria
RS886044539 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS886063926 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Sialuria
RS886063927 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Sialuria
RS966918577 Health Risk Conflicting classifications of pathogenicity Sialuria, GNE myopathy, Thrombocytopenia 12 with or without myopathy
RS986773986 Health Risk Conflicting classifications of pathogenicity GNE myopathy, Sialuria, GNE myopathy
RS1057516275 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1057516340 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1057516364 Health Risk Likely pathogenic GNE myopathy, Sialuria, GNE myopathy
RS1057516597 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1057516705 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1057516915 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1057517157 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS112061124 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS121908623 Health Risk Likely pathogenic Sialuria, Sialuria
RS1253057814 Health Risk Likely pathogenic
RS1256419231 Health Risk Likely pathogenic GNE myopathy, Sialuria, GNE myopathy
RS1455785164 Health Risk Likely pathogenic GNE myopathy, Thrombocytopenia 12 with or without myopathy, Sialuria
RS148523065 Health Risk Likely pathogenic GNE myopathy, Sialuria, GNE myopathy
RS1554657922 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1554660090 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1554661561 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1554661569 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1563946658 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1828696455 Health Risk Likely pathogenic Sialuria, GNE myopathy, Sialuria
RS1828703342 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1828914261 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1828921198 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1828929851 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1828930645 Health Risk Likely pathogenic GNE myopathy, Sialuria, GNE myopathy
RS1829027066 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
RS1829284405 Health Risk Likely pathogenic GNE myopathy, GNE myopathy
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