Taxon:

Human

Gene:

SCA8

Chromosome:

13

Location:

13q21

Description:

The SCA8 trinucleotide repeat, involved in spinocerebellar ataxia, shows contraction in association with paternal transmission and expansion in association with maternal transmission (Koob MD et al, 1999). This is not usually regarded as an imprinting effect.

Category:

Other

Record:

237

Last Modified 3/12/2015

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