Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

FAM47C

family with sequence similarity 47 member C

Chromosome
X
Cytoband
Xp21.1
Variants (rsID)
2

FAM47C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp21.1). Its official name is “family with sequence similarity 47 member C”. The reference table lists 2 variants (rsID) for this gene.

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.