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Gene entry

SALL1

spalt like transcription factor 1

Chromosome
16
Cytoband
16q12.1
Variants (rsID)
11

SALL1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q12.1). Its official name is “spalt like transcription factor 1”. The reference table lists 11 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs11645288Benignsingle nucleotide variantTownes syndrome|Townes-Brocks syndrome 1
  • rs149302006Benignsingle nucleotide variantTownes-Brocks syndrome 1|Townes syndrome
  • rs864621971Conflicting interpretationssingle nucleotide variantTownes-Brocks syndrome 1

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.