Entrez gene ID | | 51586 |
Official gene symbol | | MED15 |
Full name | | mediator complex subunit 15 |
Aliases | | ,ARC105,CAG7A,CTG7A,DKFZp686A2214,DKFZp762B1216,FLJ42282,FLJ42935,PCQAP,TIG-1,TIG1,TNRC7, |
Gene summary | | The protein encoded by this gene is a subunit of the multiprotein complexes PC2 and ARC/DRIP and may function as a transcriptional coactivator in RNA polymerase II transcription. This gene contains stretches of trinucleotide repeats and is located in the chromosome 22 region which is deleted in DiGeorge syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq] |
Location | | Chromosome: 22 Locus: 22q11.2 |
Gene position | | 20861886 - 20941919 Map Viewer |
Gene orientation | | plus |
Gene size | | 80034 bp |
Gene sequence |
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OMIM ID | | 607372 |
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