rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation.
|
29142083 |
2017 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
C |
0.800 |
GeneticVariation |
CLINVAR |
Neurodegeneration-associated mutant TREM2 proteins abortively cycle between the ER and ER-Golgi intermediate compartment.
|
28768830 |
2017 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
Neurodegeneration-associated mutant TREM2 proteins abortively cycle between the ER and ER-Golgi intermediate compartment.
|
28768830 |
2017 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
Neurodegenerative disease mutations in TREM2 reveal a functional surface and distinct loss-of-function mechanisms.
|
27995897 |
2016 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
C |
0.800 |
GeneticVariation |
CLINVAR |
Neurodegenerative disease mutations in TREM2 reveal a functional surface and distinct loss-of-function mechanisms.
|
27995897 |
2016 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
Disease-Associated Mutations of TREM2 Alter the Processing of N-Linked Oligosaccharides in the Golgi Apparatus.
|
25615530 |
2015 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (PLOSL): a new report of an Italian woman and review of the literature.
|
23399524 |
2013 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2.
|
15883308 |
2005 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
C |
0.800 |
GeneticVariation |
CLINVAR |
The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2.
|
15883308 |
2005 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
An Italian family affected by Nasu-Hakola disease with a novel genetic mutation in the TREM2 gene.
|
12754369 |
2003 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features.
|
12925681 |
2003 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype.
|
12080485 |
2002 |
rs121908402
|
TREM2;LOC105375056
|
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|