SELENOO selenoprotein O

Information
Symbol
SELENOO
Type
protein-coding
Description
selenoprotein O
Entrez Gene ID
83642
Genome
hg19
Position
chr22:50,639,440-50,656,045
Genome
hg38
Position
chr22:50,201,011-50,217,616
MIM
607917 OMIM
HGNC
HGNC:30395 HGNC
Ensembl
ENSG00000073169 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
not provided 1 0
Uncertain significance 0 158
Ranking
ClinVar
0
0
0
170
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 :
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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 SELO
MIM 607917 OMIM
HGNC HGNC:30395 HGNC
Ensembl ENSG00000073169 Ensembl
AllianceGenome HGNC:30395
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380903.7 hg38 chr22 50,201,011 50,217,616 16,606
ENST00000380903.7 hg19 chr22 50,639,440 50,656,045 16,606
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