| Name | split hand/foot malformation (ectrodactyly) type 2 |
| Synonyms | SHSF2, SHFD2 |
| NCBI Gene ID | 6463 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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SHFM2 has 13 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, functional term, phrase or reference) extracted from 3 datasets.
Click the + buttons to view associations for SHFM2 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CTD Gene-Disease Associations | diseases associated with SHFM2 gene/protein from the curated CTD Gene-Disease Associations dataset. | |
| GeneRIF Biological Term Annotations | biological terms co-occuring with SHFM2 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. | |
| OMIM Gene-Disease Associations | phenotypes associated with SHFM2 gene from the curated OMIM Gene-Disease Associations dataset. | |
