ncRv11846 MTB000142

ncRNA Putative small regulatory RNA

This is an RNA, not a coding gene: it belongs to a separate track and carries none of the protein evidence layers.

Location

2096766–2096867 (+ strand), 102 nt, on H37Rv (NC_000962.3). Intergenic (no overlapping coding sequence). Upstream neighbour Rv1846c (167 bp). Downstream neighbour Rv1847 (10 bp).

Intra-MTBC variation

Genomes surveyed145,209
Variable sites81
Variants reaching 0.1 % of genomes 0
Carriers of the most widespread variant60

Coverage control

Variant density inside this RNA: 79.4 sites/100 bp, versus 76.3 in the flanking ±500 bp (GC 70.6 %). The flanks act as an internal witness: if variants are called normally around the RNA but none becomes widespread inside it, the constraint is real rather than a sequencing gap.

Verdict: COUVERTURE OK -> invariance biologique plausible

Read with care: constraint is not function. This RNA mutates like its surroundings, but no variant spreads through the population — which is evidence of selection acting on it, not evidence of what it does. Secondary-structure pairing was tested across the RNA set and did not explain this constraint.

Predicted secondary structure

62.7 % of bases are paired in the minimum-free-energy fold (64 paired, 38 unpaired). Folded in isolation; the in vivo structure may differ (partners, co-transcriptional folding).

Legacy record

Supported by sRNA-Seq in H37Rv (see DeJesus et al. 2017)

Sources

← all RNAs