Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; required for basal RNA polymerase II transcription; homozygosity of the human MED17 L371P mutation is associated with infantile cerebral and cerebellar atrophy with poor myelination [Source:SGD;Acc:S000000824]

MED17

Chromosome V: 198,812-200,875 forward strand.

R64-1-1:BK006939.2

This gene has 1 transcript (splice variant), 17 orthologues and is a member of 1 Ensembl protein family.

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