PRDM8 Chromosome 4

PR/SET domain 8
1 variant 1 Health Risk

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What This Gene Does
This gene encodes a protein that belongs to a conserved family of histone methyltransferases that predominantly act as negative regulators of transcription. The encoded protein contains an N-terminal Su(var)3-9, Enhancer-of-zeste, and Trithorax (SET) domain and a double zinc-finger domain. Knockout of this gene in mouse results in mistargeting by neurons of the dorsal telencephalon, abnormal itch-like behavior, and impaired differentiation of rod bipolar cells. In humans, the protein has been shown to interact with the phosphatase laforin and the ubiquitin ligase malin, which regulate glycogen construction in the cytoplasm. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Gene Info
Gene Group
"Zinc fingers C2H2-type|PR/SET domain family|Putative lysine methyltransferases"
Locus Type
gene with protein product
Location
4q21.21
Ensembl
ENSG00000152784
Associated Conditions (1)
Early-onset Lafora body disease
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS863225286 Health Risk Pathogenic Early-onset Lafora body disease, Early-onset Lafora body disease
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