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APP

amyloid beta precursor protein

HCNC Approved Symbol
APP (HGNC:620)
Genomic Coordinates
21:25,880,550 - 26,171,128 (21q21.3)
Synonyms
alpha-sAPP, AD1
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Alzheimer disease 1, familial
104300AD
Cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants
605714AD

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the APP gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Memory impairment
 1 (100.0%)
Repeated speech
 1 (100.0%)