RAD21
protein-coding gene in the species Homo sapiens
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RAD21
Summary
RAD21 is a gene[1]. RAD21 ranks in the top 2% of gene entities by monthly Wikipedia readership (23 views/month).[2]
Key Facts
- RAD21's instance of is recorded as gene[3].
- RAD21 is a type of protein-coding gene[4].
- RAD21's HomoloGene ID is recorded as 38161[5].
- RAD21's genomic start is recorded as 117858174[6].
- RAD21's genomic start is recorded as 116845934[7].
- RAD21's genomic end is recorded as 117887105[8].
- RAD21's genomic end is recorded as 116874776[9].
- RAD21's ortholog is recorded as Rad21[10].
- RAD21's ortholog is recorded as Rad21[11].
- RAD21's ortholog is recorded as vtd[12].
- RAD21's ortholog is recorded as rad21b[13].
- RAD21's ortholog is recorded as rad21a[14].
- RAD21's ortholog is recorded as scc-1[15].
- RAD21's encodes is recorded as RAD21 cohesin complex component[16].
- RAD21's found in taxon is recorded as Homo sapiens[17].
- RAD21's chromosome is recorded as human chromosome 8[18].
- RAD21's genetic association is recorded as Mungan syndrome[19].
- RAD21's genetic association is recorded as Cornelia de Lange syndrome[20].
- RAD21's genetic association is recorded as Cornelia de Lange syndrome[21].
- RAD21's genetic association is recorded as sclerocornea[22].
- RAD21's genetic association is recorded as Mungan syndrome[23].
- RAD21's genetic association is recorded as acute myeloid leukemia[24].
- RAD21's strand orientation is recorded as reverse strand[25].
- RAD21's exact match is recorded as http://identifiers.org/ncbigene/5885[26].
- RAD21's cytogenetic location is recorded as 8q24.11[27].
Why It Matters
RAD21 ranks in the top 2% of gene entities by monthly Wikipedia readership (23 views/month).[2] RAD21 is known by 10 alternative names across languages and contexts.[28]