SNORD116-1

gene
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Also known as HBII-85-1

Summary

SNORD116-1 (small nucleolar RNA, C/D box 116-1, HGNC:33067) is a small nucleolar RNA gene on chromosome 15q11.2.

Predicted to be involved in RNA processing. Predicted to be located in nucleolus.

Source: NCBI Gene 100033413 — RefSeq curated summary.

At a glance

  • Gene type: non-coding (snoRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:33067
Approved symbolSNORD116-1
Namesmall nucleolar RNA, C/D box 116-1
Location15q11.2
Locus typeRNA, small nucleolar
StatusApproved
AliasesHBII-85-1
Ensembl geneENSG00000207063
Ensembl biotypesnoRNA
OMIM605436
Entrez100033413
RNAcentralURS000075CFA5 — snoRNA, 97 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 snoRNA

ENST00000384335

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000384335 — 1 exons

ExonStartEnd
ENSE000018077352505147725051571

Expression profiles

Bgee: expression breadth broad, 65 present calls, max score 98.91.

Top tissues by expression

65 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548898.91gold quality
adrenal tissueUBERON:001830391.76gold quality
kidneyUBERON:000211390.86gold quality
liverUBERON:000210788.89gold quality
adrenal glandUBERON:000236986.91gold quality
lungUBERON:000204885.74gold quality
adult mammalian kidneyUBERON:000008284.92gold quality
bloodUBERON:000017884.74gold quality
stomachUBERON:000094584.65gold quality
intestineUBERON:000016083.76gold quality
heartUBERON:000094880.07gold quality
tibial nerveUBERON:000132379.59gold quality
vermiform appendixUBERON:000115477.33gold quality
Brodmann (1909) area 9UBERON:001354076.17gold quality
endometriumUBERON:000129576.04gold quality
calcaneal tendonUBERON:000370175.12gold quality
colonUBERON:000115575.08gold quality
islet of LangerhansUBERON:000000673.61gold quality
muscle of legUBERON:000138372.62gold quality
dorsolateral prefrontal cortexUBERON:000983472.02gold quality
esophagogastric junction muscularis propriaUBERON:003584170.70gold quality
body of stomachUBERON:000116170.27gold quality
gastrocnemiusUBERON:000138870.08gold quality
left adrenal glandUBERON:000123469.13gold quality
vaginaUBERON:000099667.73gold quality
heart left ventricleUBERON:000208467.08gold quality
Ammon’s hornUBERON:000195466.06gold quality
tibial arteryUBERON:000761065.45gold quality
right atrium auricular regionUBERON:000663164.83gold quality
body of uterusUBERON:000985364.82gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.49

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 6)

  • study indicates that paternally expressed Snord116 is involved in the 24-h regulation of sleep physiological measures, suggesting that it is a candidate gene for the sleep disturbances that most individuals with Prader-Willi syndrome experience (PMID:26446116)
  • These results further support an overlapping critical deletion region involving the non-coding snoRNA SNORD116 in common in the five individuals playing a key role in contributing to the Prader-Willi syndrome phenotype (PMID:27659713)
  • The presence of macrocephaly, observed in other cases of SNORD116 deletions as well, is uncommon for the classic phenotype of the syndrome (PMID:28266014)
  • Loss of Snord116 alters cortical neuronal activity in mice: a preclinical investigation of Prader-Willi syndrome. (PMID:32426821)
  • What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders? (PMID:33082508)
  • SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndrome. (PMID:34040195)

Cross-species orthologs

0 orthologs

Paralogs (32): SNORD116-10 (ENSG00000200661), SNORD116 (ENSG00000202498), SNORD116-11 (ENSG00000206609), SNORD116-14 (ENSG00000206621), SNORD116-17 (ENSG00000206656), SNORD116-18 (ENSG00000206688), SNORD116-9 (ENSG00000206727), SNORD116-2 (ENSG00000207001), SNORD116-3 (ENSG00000207014), SNORD116-8 (ENSG00000207093), SNORD116-7 (ENSG00000207133), SNORD116-13 (ENSG00000207137), SNORD116-15 (ENSG00000207174), SNORD116-5 (ENSG00000207191), SNORD116-12 (ENSG00000207197), SNORD116-29 (ENSG00000207245), SNORD116-16 (ENSG00000207263), SNORD116-24 (ENSG00000207279), SNORD116-23 (ENSG00000207375), SNORD116-6 (ENSG00000207442), SNORD116-19 (ENSG00000207460), SNORD116 (ENSG00000212553), SNORD116-26 (ENSG00000251815), SNORD116-27 (ENSG00000251896), SNORD116-30 (ENSG00000252277), SNORD116-25 (ENSG00000252326), SNORD116 (ENSG00000252985), SNORD116-22 (ENSG00000275127), SNORD116-4 (ENSG00000275529), SNORD116-21 (ENSG00000277785), SNORD116-28 (ENSG00000278123), SNORD116-20 (ENSG00000278715)

Protein

Non-coding RNA — no protein product; not a drug target.

Function

No curated pathway, Gene-Ontology, or interaction data.

Disease & clinical

No curated disease, variant, or cancer-driver associations.

Drugs & pharmacology

No drug or pharmacology data — not an established drug target.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): strabismus