TTBK2 Chromosome 15

Tau tubulin kinase 2
42 variants 42 Health Risk

Upload your DNA to see your personal genotypes for variants in TTBK2.

What This Gene Does
This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem. [provided by RefSeq, Aug 2009]
Associated Conditions (4)
Spinocerebellar ataxia type 11
Inborn genetic diseases
TTBK2-related disorder
Spastic ataxia
Key Variants
RS117382379
Conflicting classifications of pathogenicity
Spinocerebellar ataxia type 11, Inborn genetic diseases, Spinocerebellar ataxia type 11
Health Risk
RS144199562
Conflicting classifications of pathogenicity
Spinocerebellar ataxia type 11, TTBK2-related disorder, Inborn genetic diseases
Health Risk
RS146279300
Conflicting classifications of pathogenicity
Spinocerebellar ataxia type 11, TTBK2-related disorder, Spinocerebellar ataxia type 11
Health Risk
RS146515654
Conflicting classifications of pathogenicity
Spinocerebellar ataxia type 11, Inborn genetic diseases, Spinocerebellar ataxia type 11
Health Risk
RS199635198
Conflicting classifications of pathogenicity
Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
Health Risk
RS200010694
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS200124857
Conflicting classifications of pathogenicity
Spinocerebellar ataxia type 11, Inborn genetic diseases, TTBK2-related disorder
Health Risk
RS200125366
Conflicting classifications of pathogenicity
Spinocerebellar ataxia type 11, Spastic ataxia, Inborn genetic diseases
Health Risk
RS200821440
Conflicting classifications of pathogenicity
Health Risk
RS201633321
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS202237707
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS2140986045
Conflicting classifications of pathogenicity
Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
Health Risk
All Variants (42)
RSID Category Clinical Significance Conditions
RS117382379 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Inborn genetic diseases, Spinocerebellar ataxia type 11
RS144199562 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, TTBK2-related disorder, Inborn genetic diseases
RS146279300 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, TTBK2-related disorder, Spinocerebellar ataxia type 11
RS146515654 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Inborn genetic diseases, Spinocerebellar ataxia type 11
RS199635198 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS200010694 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200124857 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Inborn genetic diseases, TTBK2-related disorder
RS200125366 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Spastic ataxia, Inborn genetic diseases
RS200821440 Health Risk Conflicting classifications of pathogenicity
RS201633321 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS202237707 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2140986045 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS36104367 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS368815985 Health Risk Conflicting classifications of pathogenicity TTBK2-related disorder, Inborn genetic diseases, TTBK2-related disorder
RS369045579 Health Risk Conflicting classifications of pathogenicity
RS370495535 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS371070916 Health Risk Conflicting classifications of pathogenicity
RS371538715 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373500080 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375070421 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS527763642 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, TTBK2-related disorder, Inborn genetic diseases
RS55833708 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Inborn genetic diseases, Spinocerebellar ataxia type 11
RS56039839 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS576737530 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Inborn genetic diseases, Spinocerebellar ataxia type 11
RS747277579 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS752400040 Health Risk Conflicting classifications of pathogenicity
RS760323338 Health Risk Conflicting classifications of pathogenicity
RS764753481 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS767042342 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS776776204 Health Risk Conflicting classifications of pathogenicity
RS781080005 Health Risk Conflicting classifications of pathogenicity Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS908445283 Health Risk Conflicting classifications of pathogenicity
RS911630565 Health Risk Conflicting classifications of pathogenicity
RS2140757755 Health Risk Likely pathogenic Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS770444240 Health Risk Likely pathogenic Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS778218227 Health Risk Likely pathogenic Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS2061886135 Health Risk Pathogenic
RS2140591830 Health Risk Pathogenic
RS2140770415 Health Risk Pathogenic
RS318240735 Health Risk Pathogenic Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS80356538 Health Risk Pathogenic Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
RS80356539 Health Risk Pathogenic Spinocerebellar ataxia type 11, Spinocerebellar ataxia type 11
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