NSD2
protein-coding gene in the species Homo sapiens
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NSD2
Summary
NSD2 is a gene[1]. NSD2 ranks in the top 2% of gene entities by monthly Wikipedia readership (21 views/month).[2]
Key Facts
- NSD2's instance of is recorded as gene[3].
- NSD2 is a type of protein-coding gene[4].
- NSD2's HomoloGene ID is recorded as 26175[5].
- NSD2's genomic start is recorded as 1873151[6].
- NSD2's genomic start is recorded as 1871393[7].
- NSD2's genomic end is recorded as 1982207[8].
- NSD2's genomic end is recorded as 1983934[9].
- NSD2's ortholog is recorded as Nsd2[10].
- NSD2's ortholog is recorded as Nsd2[11].
- NSD2's ortholog is recorded as nsd2[12].
- NSD2's encodes is recorded as Nuclear receptor binding SET domain protein 2[13].
- NSD2's encodes is recorded as Histone-lysine N-methyltransferase NSD2[14].
- NSD2's found in taxon is recorded as Homo sapiens[15].
- NSD2's chromosome is recorded as human chromosome 4[16].
- NSD2's genetic association is recorded as syndromic intellectual disability[17].
- NSD2's strand orientation is recorded as forward strand[18].
- NSD2's exact match is recorded as http://identifiers.org/ncbigene/7468[19].
- NSD2's cytogenetic location is recorded as 4p16.3[20].
- NSD2's expressed in is recorded as ventricular zone[21].
Why It Matters
NSD2 ranks in the top 2% of gene entities by monthly Wikipedia readership (21 views/month).[2]