SNORD116-1
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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
| Field | Value |
|---|---|
| HGNC ID | HGNC:33067 |
| Approved symbol | SNORD116-1 |
| Name | small nucleolar RNA, C/D box 116-1 |
| Location | 15q11.2 |
| Locus type | RNA, small nucleolar |
| Status | Approved |
| Aliases | HBII-85-1 |
| Ensembl gene | ENSG00000207063 |
| Ensembl biotype | snoRNA |
| OMIM | 605436 |
| Entrez | 100033413 |
| RNAcentral | URS000075CFA5 — 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
| Exon | Start | End |
|---|---|---|
| ENSE00001807735 | 25051477 | 25051571 |
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):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sural nerve | UBERON:0015488 | 98.91 | gold quality |
| adrenal tissue | UBERON:0018303 | 91.76 | gold quality |
| kidney | UBERON:0002113 | 90.86 | gold quality |
| liver | UBERON:0002107 | 88.89 | gold quality |
| adrenal gland | UBERON:0002369 | 86.91 | gold quality |
| lung | UBERON:0002048 | 85.74 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 84.92 | gold quality |
| blood | UBERON:0000178 | 84.74 | gold quality |
| stomach | UBERON:0000945 | 84.65 | gold quality |
| intestine | UBERON:0000160 | 83.76 | gold quality |
| heart | UBERON:0000948 | 80.07 | gold quality |
| tibial nerve | UBERON:0001323 | 79.59 | gold quality |
| vermiform appendix | UBERON:0001154 | 77.33 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 76.17 | gold quality |
| endometrium | UBERON:0001295 | 76.04 | gold quality |
| calcaneal tendon | UBERON:0003701 | 75.12 | gold quality |
| colon | UBERON:0001155 | 75.08 | gold quality |
| islet of Langerhans | UBERON:0000006 | 73.61 | gold quality |
| muscle of leg | UBERON:0001383 | 72.62 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 72.02 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 70.70 | gold quality |
| body of stomach | UBERON:0001161 | 70.27 | gold quality |
| gastrocnemius | UBERON:0001388 | 70.08 | gold quality |
| left adrenal gland | UBERON:0001234 | 69.13 | gold quality |
| vagina | UBERON:0000996 | 67.73 | gold quality |
| heart left ventricle | UBERON:0002084 | 67.08 | gold quality |
| Ammon’s horn | UBERON:0001954 | 66.06 | gold quality |
| tibial artery | UBERON:0007610 | 65.45 | gold quality |
| right atrium auricular region | UBERON:0006631 | 64.83 | gold quality |
| body of uterus | UBERON:0009853 | 64.82 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.49 |
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.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): strabismus