Gene entry
SLC1A4
solute carrier family 1 member 4
- Chromosome
- 2
- Cytoband
- 2p14
- Variants (rsID)
- 18
SLC1A4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p14). Its official name is “solute carrier family 1 member 4”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs201278558Pathogenicsingle nucleotide variantSpastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome
- rs761533681Pathogenicsingle nucleotide variantSpastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome|Inborn genetic diseases
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.