Gene entry
SPART
spartin
- Chromosome
- 13
- Cytoband
- 13q13.3
- Variants (rsID)
- 14
SPART is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q13.3). Its official name is “spartin”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs140222511Conflicting interpretationssingle nucleotide variantTroyer syndrome
- rs146398746Conflicting interpretationssingle nucleotide variantTroyer syndrome|Hereditary spastic paraplegia
- rs149730980Conflicting interpretationssingle nucleotide variantTroyer syndrome
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.