MAGOHB mago homolog B, exon junction complex subunit

Information
Symbol
MAGOHB
Type
protein-coding
Description
mago homolog B, exon junction complex subunit
Entrez Gene ID
55110
Genome
hg19
Position
chr12:10,756,792-10,766,208
Genome
hg38
Position
chr12:10,604,193-10,613,609
MIM
619552 OMIM
HGNC
HGNC:25504 HGNC
Ensembl
ENSG00000111196 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
not provided 1 0
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
12
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 MGN2
SYNONYM mago
SYNONYM magoh
MIM 619552 OMIM
HGNC HGNC:25504 HGNC
Ensembl ENSG00000111196 Ensembl
AllianceGenome HGNC:25504
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000320756.7 hg38 chr12 10,604,193 10,613,609 9,417
ENST00000539554.5 hg38 chr12 10,606,013 10,613,591 7,579
ENST00000625272.1 hg38 chr12 10,612,827 10,613,605 779
ENST00000320756.7 hg19 chr12 10,756,792 10,766,208 9,417
ENST00000539554.5 hg19 chr12 10,758,612 10,766,190 7,579
ENST00000625272.1 hg19 chr12 10,765,426 10,766,204 779
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