APOA2 gene homepage

Mutations in Hereditary Amyloidosis; consortium homepage
General information
Gene symbol APOA2
Gene name apolipoprotein A-II
Chromosome 1
Chromosomal band q23.3
Imprinted Not imprinted
Genomic reference NG_012043.1
Transcript reference NM_001643.1
Exon/intron information NM_001643.1 exon/intron table
Associated with diseases FH, FHCL1, renal failure, amyloidosis, visceral (type VIII)
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Dorota Rowczenio
Total number of public variants reported 12
Unique public DNA variants reported 9
Individuals with public variants 12
Hidden variants 3
Notes We acknowledge support from EURAMY for the development of this database.
Date created May 03, 2013
Date last updated March 23, 2020
Version APOA2:200323

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_001643.1.
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 http://www.LOVD.nl/APOA2
External URL Mutations in Hereditary Amyloidosis; consortium homepage
Graphical display APOA2 variants on cDNA sequence
HGNC 601
Entrez Gene 336
PubMed articles APOA2
OMIM - Gene 107670
OMIM - Diseases FHCL1 (hypercholesterolemia, familial, type 1 (FHCL1))
amyloidosis, visceral (type VIII)
GeneCards APOA2
GeneTests APOA2

Active transcripts




NCBI ID     

NCBI Protein ID     

00002682 1 apolipoprotein A-II NM_001643.1 NP_001634.1 12

Copyright & disclaimer
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We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.