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Gene

RNU5B-1

RNA, U5B small nuclear 1

Summary

Cytogenetic location
15q22
Coordinates
Chromosome 15: 65,304,677–65,304,793 (GRCh38)
Exons
1 exon across 0.1 kb
Also known as
U5B1
Previous symbols
RNU5B
MANE Select transcript
ENST00000363286.2NR_002757.3
Locus type
Small nuclear RNA (snRNA)

Curated reports relevant to this gene

No Genome Test report reads RNU5B-1 yet. The test sequences your whole genome, so your data includes it all the same.

How RNU5B-1 is laid out

  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
Chromosome 15, with a bracket where RNU5B-1 sits. RNU5B-1 and 22 genes near it on chromosome 15, from 64,804,735 to 65,804,734.Chromosome 1515q22p13p12p11.2p11.1q11.1q11.2q12q13.1q13.2q13.3q14q15.1q15.2q15.3q21.1q21.2q21.3q22.1q22.2q22.31q22.32q22.33q23q24.1q24.2q24.3q25.1q25.2q25.3q26.1q26.2q26.365 Mb65.2 Mb65.4 Mb65.6 Mb65.8 MbPIF1: 64,815,629–64,825,677, reverse strandPIF1PLEKHO2: 64,839,231–64,868,002, forward strandPLEKHO2: 64,841,883–64,930,920, forward strandANKDD1A: 64,911,853–64,979,845, forward strandANKDD1ASPG21: 64,954,566–64,990,312, reverse strandSPG21MTFMT: 64,990,829–65,029,652, reverse strandMTFMTSLC51B: 65,045,132–65,053,397, forward strandSLC51BRASL12: 65,053,337–65,076,690, reverse strandRASL12KBTBD13: 65,076,746–65,079,948, forward strandKBTBD13UBAP1L: 65,091,766–65,115,200, reverse strandUBAP1LPDCD7: 65,117,379–65,133,836, reverse strandPDCD7CLPX: 65,148,219–65,185,643, reverse strandCLPXCILP: 65,194,760–65,211,491, reverse strandCILPPARP16: 65,231,398–65,300,618, reverse strandPARP16RNU5B-1: 65,304,677–65,304,793, forward strandRNU5B-1IGDCC3: 65,327,127–65,378,087, reverse strandIGDCC3IGDCC4: 65,381,479–65,423,083, reverse strandIGDCC4DPP8: 65,442,463–65,517,757, reverse strandDPP8HACD3: 65,530,418–65,578,353, forward strandHACD3INTS14: 65,578,753–65,611,615, reverse strandINTS14SLC24A1: 65,611,366–65,662,034, forward strandSLC24A1DENND4A: 65,658,046–65,792,307, reverse strandDENND4ARAB11A: 65,726,054–65,894,232, forward strandRAB11ADiagram of RNU5B-1: one exon on the forward strand of chromosome 15Exon 1: 2 known disease-causing sitesExon 1: 65,304,677–65,304,793, 117 bases15′3′

Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.

Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).

Nearby genes from Ensembl release 116, on GRCh38.

Exons make up 0.1 kb of the gene's 0.1 kb.

Sequencing RNU5B-1

2

positions in RNU5B-1 where ClinVar classes a change as pathogenic or likely pathogenic

None of them falls in a region short reads find hard.

A whole genome covers all 0.1 kb of RNU5B-1, introns included, not only the 0.1 kb of exons.

Traits linked to RNU5B-1

The Human Phenotype Ontology lists these as features of the rare conditions RNU5B-1 can cause. Each trait's page lists the other genes linked to it.

Abnormality of the nervous system

Show 41 more traits

External links

Where this comes from

  • HGNC: the gene's symbol, name, other symbols and location.
  • MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
  • Data release 2026.10.17-8666dff2.

Cite this page

APA

Dante Labs. (n.d.). RNU5B-1 gene: RNA, U5B small nuclear 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/rnu5b-1

Vancouver

Dante Labs. RNU5B-1 gene: RNA, U5B small nuclear 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/rnu5b-1

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