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Gene entry

MYT1L

myelin transcription factor 1 like

Chromosome
2
Cytoband
2p25.3
Variants (rsID)
146

MYT1L is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p25.3). Its official name is “myelin transcription factor 1 like”. The reference table lists 146 variants (rsID) for this gene.

Clinically classified variants

1 reference-table entries with clinical significance.

  • rs869320675Pathogenicsingle nucleotide variantIntellectual disability, autosomal dominant 39

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.