ANCR (Angelman syndrome chromosome region)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 282 |
| Gene name | Angelman syndrome chromosome region |
| Gene symbol | ANCR |
| Synonyms (NCBI Gene) |
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| Chromosome | 15 |
| Chromosome location | 15q11-q12 |
| Summary | Angelman syndrome (AS) is characterized by developmental delay, intellectual disability, movement or balance disorders, seizures, and limitations in speech and language development. Most cases of AS are caused by deletion in the 15q11-q13 region of the ma |
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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 ANCR across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to ANCR (see Related Genes above), that are NOT already directly curated for ANCR itself -- a lead worth checking, not a confirmed association.
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