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Aliases for SHFM5 Gene

Aliases for SHFM5 Gene

  • Split Hand/Foot Malformation (Ectrodactyly) Type 5 2 3

External Ids for SHFM5 Gene

Summaries for SHFM5 Gene

GeneCards Summary for SHFM5 Gene

SHFM5 (Split Hand/Foot Malformation (Ectrodactyly) Type 5) is a Genetic Locus. Diseases associated with SHFM5 include Split-Hand/Foot Malformation 5 and Split Hand-Foot Malformation.

Additional gene information for SHFM5 Gene

No data available for Entrez Gene Summary , CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for SHFM5 Gene

Genomics for SHFM5 Gene

Genomic Locations for SHFM5 Gene

Genomic Locations for SHFM5 Gene
Unknown strand

Genomic View for SHFM5 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for SHFM5 Gene

Proteins for SHFM5 Gene

Post-translational modifications for SHFM5 Gene

No Post-translational modifications

No data available for DME Specific Peptides for SHFM5 Gene

Domains & Families for SHFM5 Gene

Graphical View of Domain Structure for InterPro Entry

No data available for Gene Families , Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for SHFM5 Gene

Function for SHFM5 Gene

Animal Model Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Phenotypes From GWAS Catalog , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for SHFM5 Gene

Localization for SHFM5 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS , Subcellular locations from the Human Protein Atlas (HPA) and Gene Ontology (GO) - Cellular Components for SHFM5 Gene

Pathways & Interactions for SHFM5 Gene

SuperPathways for SHFM5 Gene

No Data Available

Interacting Proteins for SHFM5 Gene

Gene Ontology (GO) - Biological Process for SHFM5 Gene


No data available for Pathways by source and SIGNOR curated interactions for SHFM5 Gene

Drugs & Compounds for SHFM5 Gene

No Compound Related Data Available

Transcripts for SHFM5 Gene

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for SHFM5 Gene

No ASD Table

Relevant External Links for SHFM5 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for SHFM5 Gene

Expression for SHFM5 Gene

NURSA nuclear receptor signaling pathways regulating expression of SHFM5 Gene:

No Expression Related Data Available

No data available for mRNA expression in normal human tissues , mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein differential expression in normal tissues , Protein expression , Protein tissue co-expression partners , mRNA Expression by UniProt/SwissProt , Evidence on tissue expression from TISSUES and Phenotype-based relationships between genes and organs from Gene ORGANizer for SHFM5 Gene

Orthologs for SHFM5 Gene

No data available for Orthologs and Evolution for SHFM5 Gene

Paralogs for SHFM5 Gene

No data available for Paralogs for SHFM5 Gene

Variants for SHFM5 Gene

Additional Variant Information for SHFM5 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Sequence variations from dbSNP and Humsavar , Structural Variations from Database of Genomic Variants (DGV) and Variation tolerance for SHFM5 Gene

Disorders for SHFM5 Gene

MalaCards: The human disease database

(2) MalaCards diseases for SHFM5 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
split-hand/foot malformation 5
  • shfm5
split hand-foot malformation
  • lobster-claw deformity
- elite association - COSMIC cancer census association via MalaCards
Search SHFM5 in MalaCards View complete list of genes associated with diseases
genes like me logo Genes that share disorders with SHFM5: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for SHFM5 Gene

Publications for SHFM5 Gene

  1. A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly. (PMID: 11778160) Goodman FR … Scambler PJ (American journal of human genetics 2002) 2 3 58

Products for SHFM5 Gene

Sources for SHFM5 Gene

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