| Name | Opitz G syndrome, type II |
| Description | This disorder, variously named the G, Opitz-G, or BBB syndrome, includes hypertelorism or telecanthus; laryngotracheoesophageal cleft; clefts of lip, palate, and uvula; swallowing difficulty and hoarse cry; genitourinary defects, especially hypospadias in males and splayed labia majora in females; mental retardation; and congenital heart defects.[supplied by OMIM, Jul 2002] |
| Synonyms | BBBG2, GBBB2 |
| NCBI Gene ID | 8221 |
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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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OGS2 has 2 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 2 datasets.
Click the + buttons to view associations for OGS2 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CTD Gene-Disease Associations | diseases associated with OGS2 gene/protein from the curated CTD Gene-Disease Associations dataset. | |
| OMIM Gene-Disease Associations | phenotypes associated with OGS2 gene from the curated OMIM Gene-Disease Associations dataset. | |
