Primary Identifier | MGI:3648294 | Organism | mouse, laboratory |
Chromosome | 5 | NCBI Gene Number | 231861 |
Mgi Type | protein coding gene |
description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to enable chromatin binding activity. Predicted to be located in cytosol; mitochondrion; and nucleus. Orthologous to human TNRC18 (trinucleotide repeat containing 18). PHENOTYPE: Homozygosity for a H3K9me3-binding-defective mutation causes highly penetrant embryonic death and dwarfism in surviving mice. [provided by MGI curators] |