|Name||Chromosome 16p12.2-p11.2 deletion syndrome|
|NCBI Gene ID||100526742|
|Expression in Tissues and Cell Lines||
DEL16P12.1P11.2 has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for DEL16P12.1P11.2 from the datasets below.
If available, associations are ranked by standardized value
|OMIM Gene-Disease Associations||phenotypes associated with DEL16P12.1P11.2 gene from the curated OMIM Gene-Disease Associations dataset.|