NR2E1 nuclear receptor subfamily 2 group E member 1
Gene ID: 7101, updated on 11-Apr-2024Gene type: protein coding
Also known as: TLL; TLX; XTLL
- See all available tests in GTR for this gene
- Go to complete Gene record for NR2E1
- Go to Variation Viewer for NR2E1 variants
Summary
The protein encoded by this gene is an orphan receptor involved in retinal development. The encoded protein also regulates adult neural stem cell proliferation and may be involved in control of aggressive behavior. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]
Genomic context
- Location:
- 6q21
- Sequence:
- Chromosome: 6; NC_000006.12 (108166022..108188809)
- Total number of exons:
- 10
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for NR2E1 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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