The APOE gene homepage

General information
Gene symbol APOE
Gene name apolipoprotein E
Chromosome 19
Chromosomal band q13.31
Imprinted Unknown
Genomic reference NC_000019.9
Transcript reference NM_000041.2
Exon/intron information NM_000041.2 exon/intron table
Associated with diseases AD2, AD3, ARMD1, HL3, LPG, sea blue
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 292
Unique public DNA variants reported 132
Individuals with public variants 330
Hidden variants 15
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated May 05, 2025
Version APOE:250505

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_000041.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/APOE
HGNC HGNC:613
Entrez Gene 348
PubMed articles APOE
OMIM - Gene 107741
OMIM - Diseases AD2 (Alzheimer disease, type 2 (AD-2))
AD3 (Alzheimer disease, type 3 (protection against, due to APOE3-Christchurch))
ARMD1 (macular degeneration, age-related, type 1 (ARMD-1))
HL3 (hyperlipoproteinemia, type III)
LPG (Lipoprotein glomerulopathy)
sea blue (sea-blue histiocyte disease)
HGMD APOE
GeneCards APOE
NIH Genetic Testing Registry APOE
Orphanet APOE


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00002703 19 apolipoprotein E NM_000041.2 NP_000032.1 292


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