Annotation Detail
Information
- Associated Genes
- APP
- Associated Variants
-
PSEN1 p.Met146Leu (p.M146L)
(
ENST00000700322.1,
ENST00000700317.1,
ENST00000324501.10,
ENST00000700273.1,
ENST00000700321.1,
ENST00000700323.1,
ENST00000557293.6,
ENST00000700313.1,
ENST00000700431.1,
ENST00000700265.1,
ENST00000700271.1,
ENST00000394164.5,
ENST00000700378.1,
ENST00000700320.1,
ENST00000700469.1,
ENST00000700307.1,
ENST00000700389.1,
ENST00000700324.1,
ENST00000357710.8,
ENST00000554131.6,
ENST00000700268.1,
ENST00000700437.1,
ENST00000700468.1,
ENST00000557511.5,
ENST00000700306.1,
ENST00000394157.7,
ENST00000553599.6,
ENST00000556951.6,
ENST00000700375.1,
ENST00000700312.1,
ENST00000700269.1,
ENST00000700267.1 )
PSEN1 p.Met146Val (p.M146V) ( ENST00000700312.1, ENST00000553599.6, ENST00000700375.1, ENST00000556951.6, ENST00000700269.1, ENST00000700267.1, ENST00000554131.6, ENST00000700268.1, ENST00000700437.1, ENST00000700468.1, ENST00000557511.5, ENST00000700324.1, ENST00000357710.8, ENST00000394157.7, ENST00000700306.1, ENST00000700431.1, ENST00000700323.1, ENST00000700313.1, ENST00000557293.6, ENST00000700307.1, ENST00000700469.1, ENST00000700389.1, ENST00000394164.5, ENST00000700378.1, ENST00000700271.1, ENST00000700265.1, ENST00000700320.1, ENST00000700322.1, ENST00000700321.1, ENST00000700273.1, ENST00000700317.1, ENST00000324501.10 )
PSEN1 p.Met146Leu (p.M146L) ( ENST00000394157.7, ENST00000700306.1, ENST00000557511.5, ENST00000554131.6, ENST00000700268.1, ENST00000700437.1, ENST00000700468.1, ENST00000700324.1, ENST00000357710.8, ENST00000700267.1, ENST00000700269.1, ENST00000700312.1, ENST00000700375.1, ENST00000556951.6, ENST00000553599.6, ENST00000700273.1, ENST00000700321.1, ENST00000324501.10, ENST00000700317.1, ENST00000700322.1, ENST00000700389.1, ENST00000700307.1, ENST00000700469.1, ENST00000700320.1, ENST00000700265.1, ENST00000394164.5, ENST00000700378.1, ENST00000700271.1, ENST00000700431.1, ENST00000700313.1, ENST00000557293.6, ENST00000700323.1 )
PSEN1 p.Met146Leu (p.M146L) ( ENST00000324501.10, ENST00000357710.8, ENST00000394157.7, ENST00000394164.5, ENST00000553599.6, ENST00000554131.6, ENST00000556951.6, ENST00000557293.6, ENST00000557511.5, ENST00000700265.1, ENST00000700267.1, ENST00000700268.1, ENST00000700269.1, ENST00000700271.1, ENST00000700273.1, ENST00000700306.1, ENST00000700307.1, ENST00000700312.1, ENST00000700313.1, ENST00000700317.1, ENST00000700320.1, ENST00000700321.1, ENST00000700322.1, ENST00000700323.1, ENST00000700324.1, ENST00000700375.1, ENST00000700378.1, ENST00000700389.1, ENST00000700431.1, ENST00000700437.1, ENST00000700468.1, ENST00000700469.1 )
PSEN1 p.Met146Val (p.M146V) ( ENST00000324501.10, ENST00000357710.8, ENST00000394157.7, ENST00000394164.5, ENST00000553599.6, ENST00000554131.6, ENST00000556951.6, ENST00000557293.6, ENST00000557511.5, ENST00000700265.1, ENST00000700267.1, ENST00000700268.1, ENST00000700269.1, ENST00000700271.1, ENST00000700273.1, ENST00000700306.1, ENST00000700307.1, ENST00000700312.1, ENST00000700313.1, ENST00000700317.1, ENST00000700320.1, ENST00000700321.1, ENST00000700322.1, ENST00000700323.1, ENST00000700324.1, ENST00000700375.1, ENST00000700378.1, ENST00000700389.1, ENST00000700431.1, ENST00000700437.1, ENST00000700468.1, ENST00000700469.1 )
PSEN1 p.Met146Leu (p.M146L) ( ENST00000324501.10, ENST00000357710.8, ENST00000394157.7, ENST00000394164.5, ENST00000553599.6, ENST00000554131.6, ENST00000556951.6, ENST00000557293.6, ENST00000557511.5, ENST00000700265.1, ENST00000700267.1, ENST00000700268.1, ENST00000700269.1, ENST00000700271.1, ENST00000700273.1, ENST00000700306.1, ENST00000700307.1, ENST00000700312.1, ENST00000700313.1, ENST00000700317.1, ENST00000700320.1, ENST00000700321.1, ENST00000700322.1, ENST00000700323.1, ENST00000700324.1, ENST00000700375.1, ENST00000700378.1, ENST00000700389.1, ENST00000700431.1, ENST00000700437.1, ENST00000700468.1, ENST00000700469.1 ) - Associated Disease
- Familial Alzheimer Disease (FAD)
- Source Database
- DisGeNET
- Description
- To investigate the factors that drive the Abeta42/Abeta40 ratio and amyloid pathogenesis and to investigate the possible interactions between wild-type and FAD mutant PS1, which are co-expressed in transgenic animals, we expressed the PS1 M146V knock-in allele either on wild-type PS1 (PS1M146V/+) or PS1 null (PS1M146V/-) background and crossed these alleles with the Tg2576 APP transgenic mice.
- Pubmed
- 16574645
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00515739556952576
- Year of publication
- 2006
Drugs