IGLON5 IgLON family member 5
Gene ID: 402665, updated on 17-Sep-2024Gene type: protein coding
- See all available tests in GTR for this gene
- Go to complete Gene record for IGLON5
- Go to Variation Viewer for IGLON5 variants
Summary
Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Apr 2022]
Genomic context
- Location:
- 19q13.41
- Sequence:
- Chromosome: 19; NC_000019.10 (51311644..51330891)
- Total number of exons:
- 9
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for IGLON5 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
- Variation ViewerRelated Variants
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