HTT-AS, HTT antisense RNA, 100750326

N. diseases: 1; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2798296
rs2798296
Entrez Id: 3064;100750326
Gene Symbol: HTT;HTT-AS
HTT;HTT-AS
CUI: C0020179
Disease:
Huntington Disease
0.700 GeneticVariation GWASDB Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. 22387017 2012
dbSNP: rs71180116
rs71180116
Entrez Id: 3064;100750326
Gene Symbol: HTT;HTT-AS
HTT;HTT-AS
CUI: C0020179
Disease:
Huntington Disease
CCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAG 0.700 CausalMutation CLINVAR
dbSNP: rs71180116
rs71180116
Entrez Id: 3064;100750326
Gene Symbol: HTT;HTT-AS
HTT;HTT-AS
CUI: C0020179
Disease:
Huntington Disease
CCAGCAGCAGCAGCAGCAGCAGCAG 0.700 CausalMutation CLINVAR
dbSNP: rs1217364684
rs1217364684
Entrez Id: 3064;100750326
Gene Symbol: HTT;HTT-AS
HTT;HTT-AS
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis
0.010 GeneticVariation BEFREE We also find that neuronal over-expression of CAST in hSOD1(G93A) transgenic mice inhibited production of putative neurotoxic caspase-cleaved tau and activation of Cdk5, which have been implicated in neurodegeneration in ALS models, and also reduced the formation of SOD1 oligomers. 26756888 2016
dbSNP: rs13102260
rs13102260
Entrez Id: 3064;100750326
Gene Symbol: HTT;HTT-AS
HTT;HTT-AS
CUI: C0020179
Disease:
Huntington Disease
0.010 GeneticVariation BEFREE The presence of the rs13102260 minor (A) variant on the HD disease allele was associated with delayed age of onset in familial cases, whereas the presence of the rs13102260 (A) variant on the wild-type HTT allele was associated with earlier age of onset in HD patients in an extreme case-based cohort. 25938884 2015
dbSNP: rs1313770
rs1313770
Entrez Id: 3064;100750326
Gene Symbol: HTT;HTT-AS
HTT;HTT-AS
CUI: C0020179
Disease:
Huntington Disease
0.010 GeneticVariation BEFREE Haplotype A-7-A (H1) was observed in 47 out of 48 phase-known mutant chromosomes, obtained by segregation analysis, through the haplotype analysis of rs1313770-HD/CCG-rs82334, as it also was in 120 out of 166 chromosomes constructed by means of the PHASE program. 15832309 2005