APOL2 apolipoprotein L2

Information
Symbol
APOL2
Type
protein-coding
Description
apolipoprotein L2
Entrez Gene ID
23780
Genome
hg19
Position
chr22:36,622,256-36,636,000
Genome
hg38
Position
chr22:36,226,210-36,239,954
MIM
607252 OMIM
HGNC
HGNC:619 HGNC
Ensembl
ENSG00000128335 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
66
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 :
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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 APOL-II
SYNONYM APOL3
MIM 607252 OMIM
HGNC HGNC:619 HGNC
Ensembl ENSG00000128335 Ensembl
AllianceGenome HGNC:619
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000249066.10 hg38 chr22 36,226,210 36,239,954 13,745
ENST00000358502.10 hg38 chr22 36,226,209 36,239,527 13,319
ENST00000451256.6 hg38 chr22 36,227,342 36,239,527 12,186
ENST00000358502.10 hg19 chr22 36,622,255 36,635,573 13,319
ENST00000249066.10 hg19 chr22 36,622,256 36,636,000 13,745
ENST00000451256.6 hg19 chr22 36,623,388 36,635,573 12,186
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