|Name||split hand/foot malformation (ectrodactyly) type 1 pseudogene 1|
|Synonyms||SHFM1P, DSS1P1, SEM1P1|
|NCBI Gene ID||153842|
|Expression in Tissues and Cell Lines||
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
|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 Assocation 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.|