SELENOM selenoprotein M

Information
Symbol
SELENOM
Type
protein-coding
Description
selenoprotein M
Entrez Gene ID
140606
Genome
hg19
Position
chr22:31,500,758-31,516,055
Genome
hg38
Position
chr22:31,104,772-31,120,069
MIM
610918 OMIM
HGNC
HGNC:30397 HGNC
Ensembl
ENSG00000198832 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 16
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
[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 SELM
SYNONYM SEPM
MIM 610918 OMIM
HGNC HGNC:30397 HGNC
Ensembl ENSG00000198832 Ensembl
AllianceGenome HGNC:30397
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000400299.6 hg38 chr22 31,104,777 31,107,568 2,792
ENST00000402395.5 hg38 chr22 31,104,772 31,120,069 15,298
ENST00000402395.5 hg19 chr22 31,500,758 31,516,055 15,298
ENST00000400299.6 hg19 chr22 31,500,763 31,503,554 2,792
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