Gene entry
MED25
mediator complex subunit 25
- Chromosome
- 19
- Cytoband
- 19q13.33
- Variants (rsID)
- 8
MED25 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.33). Its official name is “mediator complex subunit 25”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs145574885Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease
- rs2017698Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease type 2B2|Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome|Charcot-Marie-Tooth disease
- rs371157406Benignsingle nucleotide variantCharcot-Marie-Tooth disease type 2|Polyneuropathy|Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome|Charcot-Marie-Tooth disease
- rs145770066Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 2B2|Charcot-Marie-Tooth disease|Charcot-Marie-Tooth disease type 2|Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome|Toe walking
- rs199743509Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease
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.