RNASEH2B

Summary

RNASEH2B is a gene^[1]. RNASEH2B ranks in the top 2% of gene entities by monthly Wikipedia readership (10 views/month).^[2]

Key Facts

• RNASEH2B's instance of is recorded as gene^[3].
• RNASEH2B is a type of protein-coding gene^[4].
• RNASEH2B's HomoloGene ID is recorded as 41572^[5].
• RNASEH2B's genomic start is recorded as 51483814^[6].
• RNASEH2B's genomic start is recorded as 50909747^[7].
• RNASEH2B's genomic end is recorded as 51544592^[8].
• RNASEH2B's genomic end is recorded as 51024120^[9].
• RNASEH2B's ortholog is recorded as Rnaseh2b^[10].
• RNASEH2B's ortholog is recorded as Rnaseh2b^[11].
• RNASEH2B's ortholog is recorded as CG11164^[12].
• RNASEH2B's ortholog is recorded as rnaseh2b^[13].
• RNASEH2B's ortholog is recorded as F21D5.6^[14].
• RNASEH2B's encodes is recorded as Ribonuclease H2 subunit B^[15].
• RNASEH2B's encodes is recorded as RNASEH2B protein^[16].
• RNASEH2B's encodes is recorded as Ribonuclease H2 subunit B^[17].
• RNASEH2B's found in taxon is recorded as Homo sapiens^[18].
• RNASEH2B's chromosome is recorded as human chromosome 13^[19].
• RNASEH2B's genetic association is recorded as Aicardi-Goutieres syndrome 2^[20].
• RNASEH2B's genetic association is recorded as Aicardi-Goutieres syndrome^[21].

Why It Matters

RNASEH2B ranks in the top 2% of gene entities by monthly Wikipedia readership (10 views/month).^[2]