Name | Chromosome 22q11.2 deletion syndrome, distal |
Synonyms | C22DELQ11.2, C22DDELS |
NCBI Gene ID | 100188856 |
API | |
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Predicted Functions |
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Co-expressed Genes |
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Expression in Tissues and Cell Lines |
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DEL22Q11.2 has 91 functional associations with biological entities spanning 2 categories (functional term, phrase or reference, disease, phenotype or trait) extracted from 2 datasets.
Click the + buttons to view associations for DEL22Q11.2 from the datasets below.
If available, associations are ranked by standardized value
Dataset | Summary | |
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GeneRIF Biological Term Annotations | biological terms co-occuring with DEL22Q11.2 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. | |
OMIM Gene-Disease Associations | phenotypes associated with DEL22Q11.2 gene from the curated OMIM Gene-Disease Associations dataset. | |