LOC110011216 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 110011216 |
| Gene name | - |
| Gene symbol | LOC110011216 |
| Synonyms (NCBI Gene) |
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| Chromosome | 4 |
| Chromosome location | 4p13 |
| Summary | This biological region is found within the coding region of the paired like homeobox 2b (PHOX2B) gene on the p arm of chromosome 4, and contains an imperfect trinucleotide repeat that encodes a polyalanine tract. Expansions of this tract are a cause of co |
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Related Genes
Genes most often co-reported with LOC110011216 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC110011216 (see Related Genes above), that are NOT already directly curated for LOC110011216 itself -- a lead worth checking, not a confirmed association.
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