DGCR (DiGeorge syndrome chromosome region)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 1714 |
| Gene name | DiGeorge syndrome chromosome region |
| Gene symbol | DGCR |
| Synonyms (NCBI Gene) |
CATCH22DGSVCF
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| Chromosome | 22 |
| Chromosome location | 22q11.21-q11.23 |
| Summary | DiGeorge syndrome (DGS) comprises hypocalcemia arising from parathyroid hypoplasia, thymic hypoplasia, and outflow tract defects of the heart. Disturbance of cervical neural crest migration into the derivatives of the pharyngeal arches and pouches can acc |
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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 DGCR across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to DGCR (see Related Genes above), that are NOT already directly curated for DGCR itself -- a lead worth checking, not a confirmed association.
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