SNORD21
geneOn this page
Also known as U21
Summary
SNORD21 (small nucleolar RNA, C/D box 21, HGNC:10144) is a small nucleolar RNA gene on chromosome 1p22.1.
This gene encodes a small nucleolar RNA (snoRNA) that may be involved in biogenesis of the large (28S) ribosomal subunit. This gene is found within an intron of the RPL5 gene.
Source: NCBI Gene 6083 — 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:10144 |
| Approved symbol | SNORD21 |
| Name | small nucleolar RNA, C/D box 21 |
| Location | 1p22.1 |
| Locus type | RNA, small nucleolar |
| Status | Approved |
| Aliases | U21 |
| Ensembl gene | ENSG00000206680 |
| Ensembl biotype | snoRNA |
| OMIM | 603635 |
| Entrez | 6083 |
| RNAcentral | URS00002E0A2C — snoRNA, 95 nt, 15 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 snoRNA
ENST00000383953
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000383953 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001498963 | 92837289 | 92837383 |
Expression profiles
Bgee: expression breadth broad, 59 present calls, max score 99.75.
Top tissues by expression
59 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sural nerve | UBERON:0015488 | 99.75 | gold quality |
| liver | UBERON:0002107 | 93.46 | gold quality |
| adrenal tissue | UBERON:0018303 | 91.62 | gold quality |
| lung | UBERON:0002048 | 90.52 | gold quality |
| tibial nerve | UBERON:0001323 | 90.30 | gold quality |
| calcaneal tendon | UBERON:0003701 | 88.89 | gold quality |
| kidney | UBERON:0002113 | 85.43 | gold quality |
| blood | UBERON:0000178 | 82.85 | gold quality |
| myometrium | UBERON:0001296 | 82.50 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 82.38 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 77.62 | gold quality |
| heart | UBERON:0000948 | 77.49 | gold quality |
| lymph node | UBERON:0000029 | 77.21 | gold quality |
| muscle of leg | UBERON:0001383 | 76.07 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 75.26 | gold quality |
| prostate gland | UBERON:0002367 | 74.78 | gold quality |
| stomach | UBERON:0000945 | 74.59 | gold quality |
| small intestine | UBERON:0002108 | 72.76 | gold quality |
| islet of Langerhans | UBERON:0000006 | 72.74 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 72.05 | gold quality |
| prefrontal cortex | UBERON:0000451 | 70.17 | gold quality |
| heart left ventricle | UBERON:0002084 | 69.66 | gold quality |
| right atrium auricular region | UBERON:0006631 | 69.25 | gold quality |
| vermiform appendix | UBERON:0001154 | 68.49 | gold quality |
| intestine | UBERON:0000160 | 66.85 | gold quality |
| gastrocnemius | UBERON:0001388 | 66.24 | gold quality |
| body of stomach | UBERON:0001161 | 66.01 | gold quality |
| skin of leg | UBERON:0001511 | 65.97 | gold quality |
| tibial artery | UBERON:0007610 | 63.05 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 62.78 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Cross-species orthologs
4 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | SNORD21 | ENSDARG00000082607 |
| danio_rerio | SNORD21 | ENSDARG00000082960 |
| mus_musculus | Snord21 | ENSMUSG00000064453 |
| rattus_norvegicus | Snord21 | ENSRNOG00000058679 |
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): allergic disease, asthma, neutropenia, severe congenital, 2, autosomal dominant