MYADM myeloid associated differentiation marker

Information
Symbol
MYADM
Type
protein-coding
Description
myeloid associated differentiation marker
Entrez Gene ID
91663
Genome
hg19
Position
chr19:54,372,660-54,379,689
Genome
hg38
Position
chr19:53,869,406-53,876,435
MIM
609959 OMIM
HGNC
HGNC:7544 HGNC
Ensembl
ENSG00000179820 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
40
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
[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 SB135
MIM 609959 OMIM
HGNC HGNC:7544 HGNC
Ensembl ENSG00000179820 Ensembl
AllianceGenome HGNC:7544
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000421337.6 hg38 chr19 53,866,153 53,874,756 8,604
ENST00000391771.1 hg38 chr19 53,867,883 53,876,428 8,546
ENST00000391770.9 hg38 chr19 53,867,883 53,876,435 8,553
ENST00000391768.2 hg38 chr19 53,869,439 53,874,619 5,181
ENST00000391769.2 hg38 chr19 53,869,406 53,876,435 7,030
ENST00000421337.6 hg19 chr19 54,369,407 54,378,010 8,604
ENST00000391771.1 hg19 chr19 54,371,137 54,379,682 8,546
ENST00000391770.9 hg19 chr19 54,371,137 54,379,689 8,553
ENST00000391769.2 hg19 chr19 54,372,660 54,379,689 7,030
ENST00000391768.2 hg19 chr19 54,372,693 54,377,873 5,181
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