MED12
protein-coding gene in the species Homo sapiens
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MED12
Summary
MED12 is a gene[1]. MED12 ranks in the top 2% of gene entities by monthly Wikipedia readership (25 views/month).[2]
Key Facts
- MED12's instance of is recorded as gene[3].
- MED12 is a type of protein-coding gene[4].
- MED12's HomoloGene ID is recorded as 68441[5].
- MED12's genomic start is recorded as 70338406[6].
- MED12's genomic start is recorded as 71118543[7].
- MED12's genomic end is recorded as 70362303[8].
- MED12's genomic end is recorded as 71144103[9].
- MED12's ortholog is recorded as Med12[10].
- MED12's ortholog is recorded as Med12[11].
- MED12's ortholog is recorded as med12[12].
- MED12's ortholog is recorded as kto[13].
- MED12's encodes is recorded as Mediator complex subunit 12[14].
- MED12's found in taxon is recorded as Homo sapiens[15].
- MED12's chromosome is recorded as human X chromosome[16].
- MED12's genetic association is recorded as FG syndrome[17].
- MED12's genetic association is recorded as blepharophimosis-intellectual disability syndrome, MKB type[18].
Why It Matters
MED12 ranks in the top 2% of gene entities by monthly Wikipedia readership (25 views/month).[2] MED12 is known by 13 alternative names across languages and contexts.[19]