ZipHelixHuman GRCh38.p14
SMCR2
Smith-Magenis syndrome chromosome region, candidate 2
- Locus tag
- gene-SMCR2
- Reference assembly
- GCF_000001405.40
- Sequence
- NC_000017.11
- Gene interval
- 17,674,026–17,677,688 · - strand
- Coordinate system
- 1-based, inclusive
Published evidence
No curated experimental phenotype evidence is attached to this locus. Its annotated product describes a reference annotation, not a measured editing outcome.
Nearby genes
- PEMT · gene-PEMT — phosphatidylethanolamine N-methyltransferase
- RNU6-468P · gene-RNU6-468P — RNA, U6 small nuclear 468, pseudogene
- EEF1A1P43 · gene-EEF1A1P43 — eukaryotic translation elongation factor 1 alpha 1 pseudogene 43
- SMCR2 · gene-SMCR2 — Smith-Magenis syndrome chromosome region, candidate 2
- RAI1 · gene-RAI1 — retinoic acid induced 1
- LOC124903943 · gene-LOC124903943 — uncharacterized LOC124903943
- RAI1-AS1 · gene-RAI1-AS1 — RAI1 antisense RNA 1
Reference and sequence
NCBI reference annotation · Reference gene interval · Download gene DNA (FASTA)
Gene-level evidence does not identify a validated nucleotide edit. Evaluate the study’s strain and conditions before applying an observation to another background.