APOO apolipoprotein O

Information
Symbol
APOO
Type
protein-coding
Description
apolipoprotein O
Entrez Gene ID
79135
Genome
hg19
Position
chrX:23,851,470-23,926,055
Genome
hg38
Position
chrX:23,833,353-23,907,938
MIM
300753 OMIM
HGNC
HGNC:28727 HGNC
Ensembl
ENSG00000184831 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 4
Likely benign 0 6
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 0 6
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 FAM121B
SYNONYM MIC26
SYNONYM MICOS26
SYNONYM Mic23
SYNONYM My025
MIM 300753 OMIM
HGNC HGNC:28727 HGNC
Ensembl ENSG00000184831 Ensembl
AllianceGenome HGNC:28727
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000379226.9 hg38 chrX 23,833,353 23,907,938 74,586
ENST00000379226.9 hg19 chrX 23,851,470 23,926,055 74,586
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