APP Chromosome 21
Amyloid beta precursor protein
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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
RS1305531440
Conflicting classifications of pathogenicity
Alzheimer disease, Hereditary cerebral hemorrhage with amyloidosis, Alzheimer disease
Health Risk
RS137865262
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
RS139819006
Conflicting classifications of pathogenicity
Alzheimer disease, Cerebral amyloid angiopathy, APP-related
Health Risk
RS139885956
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
RS145081708
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
RS145371658
Conflicting classifications of pathogenicity
Alzheimer disease, Inborn genetic diseases, Alzheimer disease
Health Risk
RS147485129
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
RS149995579
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
RS1800557
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
RS199587668
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
RS199887707
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
RS199890425
Conflicting classifications of pathogenicity
Alzheimer disease, Alzheimer disease
Health Risk
All Variants (52)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS63751039 | Health Risk | Pathogenic | ABeta amyloidosis, Arctic type, Alzheimer disease type 1 |
| RS63750734 | Health Risk | Pathogenic/Likely pathogenic | Alzheimer disease type 1, Alzheimer disease, Alzheimer disease type 1 |