SHFM5 Gene

Name split hand/foot malformation (ectrodactyly) type 5
NCBI Gene ID 171157
API
Download Associations
Predicted Functions View SHFM5's ARCHS4 Predicted Functions.
Co-expressed Genes View SHFM5's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View SHFM5's ARCHS4 Predicted Functions.

Functional Associations

SHFM5 has 3 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 2 datasets.

Click the + buttons to view associations for SHFM5 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with SHFM5 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with SHFM5 gene from the curated OMIM Gene-Disease Associations dataset.