Gene entry

SLC39A4

solute carrier family 39 member 4

Chromosome: 8
Cytoband: 8q24.3
Variants (rsID): 2

SLC39A4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q24.3). Its official name is “solute carrier family 39 member 4”. The reference table lists 2 variants (rsID) for this gene.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Clinically classified variants

2 reference-table entries with clinical significance.

rs1871534Benignsingle nucleotide variantHereditary acrodermatitis enteropathica
rs121434287Likely pathogenicsingle nucleotide variantHereditary acrodermatitis enteropathica

Public references

NCBI Gene
Ensembl
ClinVar

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