MAGEC2 MAGE family member C2

Information
Symbol
MAGEC2
Type
protein-coding
Description
MAGE family member C2
Entrez Gene ID
51438
Genome
hg19
Position
chrX:141,290,128-141,293,076
Genome
hg38
Position
chrX:142,202,342-142,205,290
MIM
300468 OMIM
HGNC
HGNC:13574 HGNC
Ensembl
ENSG00000046774 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 12
not provided 6 0
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
48
0
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 CT10
SYNONYM HCA587
SYNONYM MAGEE1
MIM 300468 OMIM
HGNC HGNC:13574 HGNC
Ensembl ENSG00000046774 Ensembl
AllianceGenome HGNC:13574
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000247452.4 hg38 chrX 142,202,342 142,205,290 2,949
ENST00000247452.4 hg19 chrX 141,290,128 141,293,076 2,949
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