NRXN1-DT (NRXN1 divergent transcript)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 730100 |
| Gene name | NRXN1 divergent transcript |
| Gene symbol | NRXN1-DT |
| Synonyms (NCBI Gene) |
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| Chromosome | 2 |
| Chromosome location | 2p16.3 |
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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Related Genes
Genes most often co-reported with NRXN1-DT across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to NRXN1-DT (see Related Genes above), that are NOT already directly curated for NRXN1-DT itself -- a lead worth checking, not a confirmed association.
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