MAG myelin associated glycoprotein

Information
Symbol
MAG
Type
protein-coding
Description
myelin associated glycoprotein
Entrez Gene ID
4099
Genome
hg19
Position
chr19:35,783,064-35,804,710
Genome
hg38
Position
chr19:35,292,161-35,313,807
MIM
159460 OMIM
HGNC
HGNC:6783 HGNC
Ensembl
ENSG00000105695 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 6
Benign 0 56
Likely benign 0 232
Conflicting classifications of pathogenicity 0 6
Uncertain significance 0 266
Ranking
ClinVar
0
0
74
474
4
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM GMA
SYNONYM S-MAG
SYNONYM SIGLEC-4A
SYNONYM SIGLEC4
SYNONYM SIGLEC4A
SYNONYM SPG75
MIM 159460 OMIM
HGNC HGNC:6783 HGNC
Ensembl ENSG00000105695 Ensembl
AllianceGenome HGNC:6783
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537831.2 hg38 chr19 35,292,161 35,313,804 21,644
ENST00000597035.5 hg38 chr19 35,292,161 35,299,796 7,636
ENST00000361922.8 hg38 chr19 35,292,134 35,313,804 21,671
ENST00000392213.8 hg38 chr19 35,292,161 35,313,807 21,647
ENST00000361922.8 hg19 chr19 35,783,037 35,804,707 21,671
ENST00000597035.5 hg19 chr19 35,783,064 35,790,699 7,636
ENST00000537831.2 hg19 chr19 35,783,064 35,804,707 21,644
ENST00000392213.8 hg19 chr19 35,783,064 35,804,710 21,647
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