MAGEL2 MAGE family member L2

Information
Symbol
MAGEL2
Type
protein-coding
Description
MAGE family member L2
Entrez Gene ID
54551
Genome
hg19
Position
chr15:23,888,696-23,893,014
Genome
hg38
Position
chr15:23,643,549-23,647,867
MIM
605283 OMIM
HGNC
HGNC:6814 HGNC
Ensembl
ENSG00000254585 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 10 88
Likely pathogenic 0 62
Benign 0 96
Likely benign 0 424
Conflicting classifications of pathogenicity 0 122
not provided 4 0
Uncertain significance 0 1,052
Ranking
ClinVar
0
0
402
1,238
16
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 NDNL1
SYNONYM PWLS
SYNONYM SHFYNG
SYNONYM nM15
MIM 605283 OMIM
HGNC HGNC:6814 HGNC
Ensembl ENSG00000254585 Ensembl
AllianceGenome HGNC:6814
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000650528.1 hg38 chr15 23,643,549 23,647,867 4,319
ENST00000650528.1 hg19 chr15 23,888,696 23,893,014 4,319
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