SHFM1P1 Gene

Name split hand/foot malformation (ectrodactyly) type 1 pseudogene 1
Synonyms DSS1P1, SHFM1P, SEM1P1
NCBI Gene ID 153842
API
Download Associations
Predicted Functions View SHFM1P1's ARCHS4 Predicted Functions.
Co-expressed Genes View SHFM1P1's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View SHFM1P1's ARCHS4 Predicted Functions.

Functional Associations

SHFM1P1 has 10 functional associations with biological entities spanning 4 categories (molecular profile, disease, phenotype or trait, cell line, cell type or tissue, gene, protein or microRNA) extracted from 4 datasets.

Click the + buttons to view associations for SHFM1P1 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
ChEA Transcription Factor Binding Site Profiles transcription factor binding site profiles with transcription factor binding evidence at the promoter of SHFM1P1 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
ChEA Transcription Factor Targets transcription factors binding the promoter of SHFM1P1 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
DISEASES Experimental Gene-Disease Association Evidence Scores diseases associated with SHFM1P1 gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
GTEx Tissue Gene Expression Profiles tissues with high or low expression of SHFM1P1 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.