|Name||Chromosome 22q11.2 deletion syndrome, distal|
|NCBI Gene ID||100188856|
|Expression in Tissues and Cell Lines||
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
|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.|