SMN2
protein-coding gene in the species Homo sapiens
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SMN2
Summary
SMN2 is a gene[1]. SMN2 ranks in the top 2% of gene entities by monthly Wikipedia readership (27 views/month).[2]
Key Facts
- SMN2's instance of is recorded as gene[3].
- SMN2 is a type of protein-coding gene[4].
- SMN2's HomoloGene ID is recorded as 292[5].
- SMN2's genomic start is recorded as 69345350[6].
- SMN2's genomic start is recorded as 70220768[7].
- SMN2's genomic start is recorded as 70049638[8].
- SMN2's genomic end is recorded as 70078522[9].
- SMN2's genomic end is recorded as 69374349[10].
- SMN2's genomic end is recorded as 70249769[11].
- SMN2's ortholog is recorded as Smn1[12].
- SMN2's ortholog is recorded as Smn1[13].
- SMN2's ortholog is recorded as smn1[14].
- SMN2's encodes is recorded as Survival of motor neuron 2, centromeric[15].
- SMN2's found in taxon is recorded as Homo sapiens[16].
- SMN2's chromosome is recorded as human chromosome 5[17].
- SMN2's genetic association is recorded as juvenile spinal muscular atrophy[18].
- SMN2's strand orientation is recorded as forward strand[19].
- SMN2's exact match is recorded as http://identifiers.org/ncbigene/6607[20].
Why It Matters
SMN2 ranks in the top 2% of gene entities by monthly Wikipedia readership (27 views/month).[2] SMN2 is known by 7 alternative names across languages and contexts.[21]