MAG Chromosome 19

Myelin associated glycoprotein
16 variants 16 Health Risk

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What This Gene Does
The protein encoded by this gene is a type I membrane protein and member of the immunoglobulin superfamily. It is thought to be involved in the process of myelination. It is a lectin that binds to sialylated glycoconjugates and mediates certain myelin-neuron cell-cell interactions. Three alternatively spliced transcripts encoding different isoforms have been described for this gene. [provided by RefSeq, Nov 2010]
Gene Info
Gene Group
"C2-set domain containing|I-set domain containing|Sialic acid binding Ig like lectins"
Locus Type
gene with protein product
Location
19q13.1
Ensembl
ENSG00000105695
Associated Conditions (5)
Hereditary spastic paraplegia
Hereditary spastic paraplegia 75
MAG-related disorder
Nonpapillary renal cell carcinoma
Inborn genetic diseases
Key Variants
All Variants (16)
RSID Category Clinical Significance Conditions
RS144553163 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia, Hereditary spastic paraplegia 75, MAG-related disorder
RS200576970 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 75, Inborn genetic diseases, Hereditary spastic paraplegia 75
RS200695849 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS201985838 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS35237014 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 75, MAG-related disorder, Hereditary spastic paraplegia 75
RS778356275 Health Risk Conflicting classifications of pathogenicity Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS1555763342 Health Risk Likely pathogenic
RS2513582014 Health Risk Likely pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS2513601109 Health Risk Likely pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS2066456693 Health Risk Pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS2301600 Health Risk Pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS587777229 Health Risk Pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS770601245 Health Risk Pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS770788013 Health Risk Pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS771777424 Health Risk Pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
RS2066519362 Health Risk Pathogenic/Likely pathogenic Hereditary spastic paraplegia 75, Hereditary spastic paraplegia 75
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