APOM apolipoprotein M

Information
Symbol
APOM
Type
protein-coding
Description
apolipoprotein M
Entrez Gene ID
55937
Genome
hg19
Position
chr6:31,623,671-31,625,987
Genome
hg38
Position
chr6:31,655,894-31,658,210
MIM
606907 OMIM
HGNC
HGNC:13916 HGNC
Ensembl
ENSG00000204444 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
not provided 3 0
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
18
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 G3a
SYNONYM HSPC336
SYNONYM NG20
SYNONYM apo-M
MIM 606907 OMIM
HGNC HGNC:13916 HGNC
Ensembl ENSG00000204444 Ensembl
AllianceGenome HGNC:13916
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000375916.4 hg38 chr6 31,655,894 31,658,210 2,317
ENST00000375918.6 hg38 chr6 31,652,416 31,658,082 5,667
ENST00000375920.8 hg38 chr6 31,652,417 31,658,210 5,794
ENST00000375918.6 hg19 chr6 31,620,193 31,625,859 5,667
ENST00000375920.8 hg19 chr6 31,620,194 31,625,987 5,794
ENST00000375916.4 hg19 chr6 31,623,671 31,625,987 2,317
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