SYBU, syntabulin, 55638

N. diseases: 120; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1314736087
rs1314736087
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C0338656
Disease:
Impaired cognition
0.010 GeneticVariation BEFREE Unexpectedly, we found that 4R NM human tau (hTau) exhibited abnormal dynamics in young mice that were lost with the P301L mutation, including elevated protein stability and hyperphosphorylation, which were associated with cognitive impairment in 5-month old rT1 mice. 31685653 2020
dbSNP: rs1314736087
rs1314736087
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C0949664
Disease:
Tauopathies
0.010 GeneticVariation BEFREE Overall, our genetically matched mice have revealed that 4R NM hTau over expression is pathogenic in a manner distinct from classical aging-related tauopathy, underlining the importance of assaying the effects of transgenic disease-related proteins at appropriate stages in life.<b>SIGNIFICANCE STATEMENT</b>Due to differences in creation of transgenic lines, the pathological properties the P301L mutation confers to the tau protein <i>in vivo</i> have remained elusive, perhaps contributing to the lack of disease-modifying therapies for tauopathies. 31685653 2020
dbSNP: rs1314736087
rs1314736087
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C4020732
Disease:
Mitochondrial abnormalities
0.010 GeneticVariation BEFREE We also show that NM hTau exhibits stronger binding to microtubules than P301L hTau, and is associated with mitochondrial abnormalities. 31685653 2020
dbSNP: rs1314736087
rs1314736087
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C0236642
Disease:
Pick Disease of the Brain
0.010 GeneticVariation BEFREE Then, we investigated if an altered tau, such as the P301L mutated protein associated with frontotemporal dementia, could produce nuclear pathology. 18583940 2008
dbSNP: rs1314736087
rs1314736087
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C0338451
Disease:
Frontotemporal dementia
0.010 GeneticVariation BEFREE Then, we investigated if an altered tau, such as the P301L mutated protein associated with frontotemporal dementia, could produce nuclear pathology. 18583940 2008
dbSNP: rs1416313401
rs1416313401
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C0031511
Disease:
Pheochromocytoma
0.010 GeneticVariation BEFREE From analysis of naturally occurring pVHL mutants, it seems that only point mutations such as pVHL(Y98H) and pVHL(Y112H) (that predispose to haemangioblastoma and phaeochromocytoma, but not to renal cell carcinoma) disrupt pVHL's microtubule-stabilizing function. 12510195 2003
dbSNP: rs1416313401
rs1416313401
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C0206734
Disease:
Hemangioblastoma
0.010 GeneticVariation BEFREE From analysis of naturally occurring pVHL mutants, it seems that only point mutations such as pVHL(Y98H) and pVHL(Y112H) (that predispose to haemangioblastoma and phaeochromocytoma, but not to renal cell carcinoma) disrupt pVHL's microtubule-stabilizing function. 12510195 2003
dbSNP: rs1416313401
rs1416313401
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C4551683
Disease:
Adrenal Gland Pheochromocytoma
0.010 GeneticVariation BEFREE From analysis of naturally occurring pVHL mutants, it seems that only point mutations such as pVHL(Y98H) and pVHL(Y112H) (that predispose to haemangioblastoma and phaeochromocytoma, but not to renal cell carcinoma) disrupt pVHL's microtubule-stabilizing function. 12510195 2003
dbSNP: rs1416313401
rs1416313401
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C0279702
Disease:
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 GeneticVariation BEFREE From analysis of naturally occurring pVHL mutants, it seems that only point mutations such as pVHL(Y98H) and pVHL(Y112H) (that predispose to haemangioblastoma and phaeochromocytoma, but not to renal cell carcinoma) disrupt pVHL's microtubule-stabilizing function. 12510195 2003
dbSNP: rs1416313401
rs1416313401
Entrez Id: 55638
Gene Symbol: SYBU
SYBU
CUI: C0007134
Disease:
Renal Cell Carcinoma
0.010 GeneticVariation BEFREE From analysis of naturally occurring pVHL mutants, it seems that only point mutations such as pVHL(Y98H) and pVHL(Y112H) (that predispose to haemangioblastoma and phaeochromocytoma, but not to renal cell carcinoma) disrupt pVHL's microtubule-stabilizing function. 12510195 2003