MED17
protein-coding gene in the species Homo sapiens
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MED17
Summary
MED17 is a gene[1]. MED17 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2]
Key Facts
- MED17's instance of is recorded as gene[3].
- MED17 is a type of protein-coding gene[4].
- MED17's HomoloGene ID is recorded as 3151[5].
- MED17's genomic start is recorded as 93784227[6].
- MED17's genomic start is recorded as 93517393[7].
- MED17's genomic end is recorded as 93547861[8].
- MED17's genomic end is recorded as 93814963[9].
- MED17's ortholog is recorded as Med17[10].
- MED17's ortholog is recorded as Med17[11].
- MED17's ortholog is recorded as MED17[12].
- MED17's ortholog is recorded as med17[13].
- MED17's ortholog is recorded as mdt-17[14].
- MED17's encodes is recorded as Mediator complex subunit 17[15].
- MED17's found in taxon is recorded as Homo sapiens[16].
- MED17's chromosome is recorded as human chromosome 11[17].
- MED17's genetic association is recorded as infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly[18].
- MED17's strand orientation is recorded as forward strand[19].
- MED17's exact match is recorded as http://identifiers.org/ncbigene/9440[20].
- MED17's cytogenetic location is recorded as 11q21[21].
- MED17's expressed in is recorded as sural nerve[22].
- MED17's expressed in is recorded as ventricular zone[23].
- MED17's expressed in is recorded as ganglionic eminence[24].
- MED17's expressed in is recorded as Achilles tendon[25].
- MED17's expressed in is recorded as left ovary[26].
- MED17's expressed in is recorded as right ovary[27].
Why It Matters
MED17 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2]