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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 synpolydactyly.

No data available for Entrez Gene 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 Location for SHFM5 Gene

Unknown strand

Genomic View for SHFM5 Gene

Cytogenetic band:

No data available for 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 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

No data available for Molecular function , Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Phenotypes , 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 and Gene Ontology (GO) - Cellular Components for SHFM5 Gene

Pathways 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 for SHFM5 Gene

Transcripts for SHFM5 Gene

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

No Expression Related Data Available

Primer Products

In Situ Assay Products

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 , mRNA Expression by UniProt/SwissProt and Expression partners 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

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 Relevant External Links for SHFM5 Gene

Disorders for SHFM5 Gene

MalaCards: The human disease database

MalaCards: The human disease database.

Search for SHFM5 Gene in MalaCards »

(3) Diseases for SHFM5 Gene

genes like me logo Genes that share disorders with SHFM5: view

No data available for OMIM , UniProtKB/Swiss-Prot , University of Copenhagen DISEASES , Novoseek inferred disease relationships , 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 F.R. … Scambler P.J. (Am. J. Hum. Genet. 2002) 2 3

Products for SHFM5 Gene

Sources for SHFM5 Gene

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