LOC110599567 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 110599567 |
| Gene name | - |
| Gene symbol | LOC110599567 |
| Synonyms (NCBI Gene) |
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| Chromosome | 7 |
| Chromosome location | 7q36.3 |
| Summary | This region is a highly variable minisatellite region found within an intron of the on the protein tyrosine phosphatase, receptor type N2 (PTPRN2) gene, on the q arm of chromosome 7. The D7S22 minisatellite is an unstable GC-rich variable number tandem re |
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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 LOC110599567 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC110599567 (see Related Genes above), that are NOT already directly curated for LOC110599567 itself -- a lead worth checking, not a confirmed association.
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