APP Chromosome 21

Amyloid beta precursor protein
52 variants 52 Health Risk

Upload your DNA to see your personal genotypes for variants in APP.

What This Gene Does
This gene encodes a cell surface receptor and transmembrane precursor protein that is cleaved by secretases to form a number of peptides. Some of these peptides are secreted and can bind to the acetyltransferase complex APBB1/TIP60 to promote transcriptional activation, while others form the protein basis of the amyloid plaques found in the brains of patients with Alzheimer disease. In addition, two of the peptides are antimicrobial peptides, having been shown to have bacteriocidal and antifungal activities. Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2014]
Gene Info
Gene Group
Receptor ligands
Locus Type
gene with protein product
Location
21q21.3
Ensembl
ENSG00000142192
Associated Conditions (19)
Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis
Cerebral amyloid angiopathy
APP-related
Inborn genetic diseases
Early-onset dementia of unclear type
Alzheimer disease type 1
APP-related disorder
Primary degenerative dementia of the Alzheimer type
presenile onset
CEREBRAL AMYLOID ANGIOPATHY
APP-RELATED
PIEDMONT VARIANT
ABeta amyloidosis
Iowa type
dutch type
Italian type
ABetaA21G amyloidosis
Arctic type
Key Variants
All Variants (52)
RSID Category Clinical Significance Conditions
RS1305531440 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Hereditary cerebral hemorrhage with amyloidosis, Alzheimer disease
RS137865262 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS139819006 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Cerebral amyloid angiopathy, APP-related
RS139885956 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS145081708 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS145371658 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Inborn genetic diseases, Alzheimer disease
RS147485129 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS149995579 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS1800557 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS199587668 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS199887707 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS199890425 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS200088099 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS200103591 Health Risk Conflicting classifications of pathogenicity Early-onset dementia of unclear type, Alzheimer disease, Early-onset dementia of unclear type
RS200725014 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS200978018 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS201022619 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS201269325 Health Risk Conflicting classifications of pathogenicity Cerebral amyloid angiopathy, APP-related, Hereditary cerebral hemorrhage with amyloidosis
RS201290605 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS201466202 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Inborn genetic diseases, Alzheimer disease type 1
RS201668897 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Inborn genetic diseases, Alzheimer disease
RS201937048 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS202218688 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Inborn genetic diseases, Alzheimer disease
RS372642708 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Inborn genetic diseases, Alzheimer disease
RS527890624 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, APP-related disorder, Alzheimer disease
RS63749953 Health Risk Conflicting classifications of pathogenicity APP-related disorder, APP-related disorder
RS750279232 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS752361848 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease type 1, Alzheimer disease
RS761439332 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Alzheimer disease, Inborn genetic diseases
RS765657163 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Alzheimer disease
RS768238394 Health Risk Conflicting classifications of pathogenicity Alzheimer disease, Cerebral amyloid angiopathy, APP-related
RS145564988 Health Risk Likely pathogenic
RS199820754 Health Risk Likely pathogenic Alzheimer disease type 1, Cerebral amyloid angiopathy, APP-related
RS2146237857 Health Risk Likely pathogenic Alzheimer disease type 1, Alzheimer disease type 1
RS63750064 Health Risk Likely pathogenic
RS63750066 Health Risk Likely pathogenic Alzheimer disease type 1, Alzheimer disease, Primary degenerative dementia of the Alzheimer type
RS63750921 Health Risk Likely pathogenic CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
RS193922916 Health Risk Pathogenic Alzheimer disease, Alzheimer disease
RS2146237965 Health Risk Pathogenic Alzheimer disease, Alzheimer disease
RS281865161 Health Risk Pathogenic Alzheimer disease type 1, Alzheimer disease, APP-related disorder
RS63749810 Health Risk Pathogenic ABeta amyloidosis, Iowa type, Alzheimer disease
RS63749964 Health Risk Pathogenic Alzheimer disease type 1, Alzheimer disease type 1
RS63750264 Health Risk Pathogenic Alzheimer disease, Alzheimer disease type 1, Cerebral amyloid angiopathy
RS63750399 Health Risk Pathogenic Alzheimer disease type 1, Alzheimer disease, Alzheimer disease type 1
RS63750579 Health Risk Pathogenic ABeta amyloidosis, dutch type, Alzheimer disease
RS63750643 Health Risk Pathogenic Alzheimer disease type 1, Alzheimer disease, Alzheimer disease type 1
RS63750671 Health Risk Pathogenic ABetaA21G amyloidosis, Alzheimer disease type 1, Alzheimer disease
RS63750851 Health Risk Pathogenic Alzheimer disease, Alzheimer disease
RS63750868 Health Risk Pathogenic APP-related disorder, APP-related disorder
RS63750973 Health Risk Pathogenic Alzheimer disease type 1, Alzheimer disease, Alzheimer disease type 1
Sign Up to Analyze Your DNA Log In