Gene entry
KDM5C
lysine demethylase 5C
- Chromosome
- X
- Cytoband
- Xp11.22
- Variants (rsID)
- 4
KDM5C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.22). Its official name is “lysine demethylase 5C”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs199422235Likely pathogenicsingle nucleotide variantSyndromic X-linked intellectual disability Claes-Jensen type|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.