MED25
mediator complex subunit 25
Pathway candidate — not linked to PFS or PSSD by any record here
Gene summary
A protein-coding gene on chromosome 19 (cell signaling and transcription factors). Encodes a component of the transcriptional coactivator complex termed the Mediator complex. This complex is required for transcription of most RNA polymerase II-dependent genes.
Source: NCBI Gene, accessed 2026-10-07.
Protein reference (UniProt)
- Protein
Mediator of RNA polymerase II transcription subunit 25
- Function
Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors. Required for RARA/RXRA-mediated transcription.
- Subcellular location
Nucleus.
- Tissue specificity
Ubiquitously expressed. Highest levels in brain, heart, kidney, peripheral leukocytes, placenta, skeletal muscle and spleen.
- Associated conditions
Charcot-Marie-Tooth disease, axonal, type 2B2 (CMT2B2); Basel-Vanagaite-Smirin-Yosef syndrome (BVSYS).
Source: UniProtKB/Swiss-Prot Q71SY5, release 2026_03, licensed CC BY 4.0. This is the protein’s normal biology, not evidence about post-drug syndromes; associated conditions are inherited disorders of the gene, not PFS, PSSD or PRSD.
Why its pathway is in the library
General signaling/transcription machinery; no direct post-drug-syndrome link established for most members — included for completeness of the panel.
Written for the whole signaling & transcription family, not for MED25 specifically.
Mentioned in 0 corpus records
No corpus record names MED25 directly yet. It is in the library because it sits in a pathway the corpus tracks (Signaling & transcription).
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