MAGED4B MAGE family member D4B

Information
Symbol
MAGED4B
Type
protein-coding
Description
MAGE family member D4B
Entrez Gene ID
81557
Genome
hg19
Position
chrX:51,804,923-51,812,315
Genome
hg38
Position
chrX:52,061,827-52,069,219
MIM
300765 OMIM
HGNC
HGNC:22880 HGNC
Ensembl
ENSG00000187243 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
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
MIM 300765 OMIM
HGNC HGNC:22880 HGNC
Ensembl ENSG00000187243 Ensembl
AllianceGenome HGNC:22880
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000360134.10 hg38 chrX 52,061,827 52,069,198 7,372
ENST00000335504.10 hg38 chrX 52,061,827 52,069,183 7,357
ENST00000485287.5 hg38 chrX 52,061,827 52,069,219 7,393
ENST00000497164.5 hg38 chrX 52,061,827 52,069,182 7,356
ENST00000497164.5 hg19 chrX 51,804,923 51,812,278 7,356
ENST00000335504.10 hg19 chrX 51,804,923 51,812,279 7,357
ENST00000360134.10 hg19 chrX 51,804,923 51,812,294 7,372
ENST00000485287.5 hg19 chrX 51,804,923 51,812,315 7,393
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