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Gene entry

SIM2

SIM bHLH transcription factor 2

Chromosome
21
Cytoband
21q22.13
Variants (rsID)
21

SIM2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q22.13). Its official name is “SIM bHLH transcription factor 2”. The reference table lists 21 variants (rsID) for this gene.

Clinically classified variants

1 reference-table entries with clinical significance.

  • rs2073601Not classifiedmissense_variantDown Syndrome|Chromosomal Triplication|Scoliosis

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.