APOL4 apolipoprotein L4

Information
Symbol
APOL4
Type
protein-coding
Description
apolipoprotein L4
Entrez Gene ID
80832
Genome
hg19
Position
chr22:36,585,177-36,600,879
Genome
hg38
Position
chr22:36,189,129-36,204,833
MIM
607254 OMIM
HGNC
HGNC:14867 HGNC
Ensembl
ENSG00000100336 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
14
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 APOL-IV
SYNONYM APOLIV
MIM 607254 OMIM
HGNC HGNC:14867 HGNC
Ensembl ENSG00000100336 Ensembl
AllianceGenome HGNC:14867
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000683024.1 hg38 chr22 36,189,128 36,201,809 12,682
ENST00000616056.4 hg38 chr22 36,189,129 36,204,840 15,712
ENST00000397275.6 hg38 chr22 36,197,455 36,204,743 7,289
ENST00000332987.5 hg38 chr22 36,190,797 36,204,806 14,010
ENST00000352371.5 hg38 chr22 36,189,129 36,204,833 15,705
ENST00000684666.1 hg38 chr22 36,189,128 36,202,191 13,064
ENST00000683024.1 hg19 chr22 36,585,176 36,597,855 12,680
ENST00000684666.1 hg19 chr22 36,585,176 36,598,237 13,062
ENST00000352371.5 hg19 chr22 36,585,177 36,600,879 15,703
ENST00000616056.4 hg19 chr22 36,585,177 36,600,886 15,710
ENST00000332987.5 hg19 chr22 36,586,845 36,600,852 14,008
ENST00000397275.6 hg19 chr22 36,593,501 36,600,789 7,289
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