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Aliases for DFNA59 Gene

Aliases for DFNA59 Gene

  • Deafness, Autosomal Dominant 59 2 3

External Ids for DFNA59 Gene

Previous GeneCards Identifiers for DFNA59 Gene

  • GC00U922893

Summaries for DFNA59 Gene

GeneCards Summary for DFNA59 Gene

DFNA59 (Deafness, Autosomal Dominant 59) is a Genetic Locus. Diseases associated with DFNA59 include Deafness, Autosomal Dominant 59 and Autosomal Dominant Nonsyndromic Deafness.

Additional gene information for DFNA59 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 DFNA59 Gene

Genomics for DFNA59 Gene

Genomic Locations for DFNA59 Gene

Genomic Locations for DFNA59 Gene
Unknown strand

Genomic View for DFNA59 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for DFNA59 Gene

Proteins for DFNA59 Gene

Post-translational modifications for DFNA59 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNA59 Gene

Domains & Families for DFNA59 Gene

Gene Families for DFNA59 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNA59: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNA59 Gene

Function for DFNA59 Gene

Animal Model Products

Clone 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 DFNA59 Gene

Localization for DFNA59 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 DFNA59 Gene

Pathways & Interactions for DFNA59 Gene

SuperPathways for DFNA59 Gene

No Data Available

Interacting Proteins for DFNA59 Gene

Gene Ontology (GO) - Biological Process for DFNA59 Gene


No data available for Pathways by source and SIGNOR curated interactions for DFNA59 Gene

Drugs & Compounds for DFNA59 Gene

No Compound Related Data Available

Transcripts for DFNA59 Gene

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for DFNA59 Gene

No ASD Table

Relevant External Links for DFNA59 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for DFNA59 Gene

Expression for DFNA59 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNA59 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 DFNA59 Gene

Orthologs for DFNA59 Gene

No data available for Orthologs and Evolution for DFNA59 Gene

Paralogs for DFNA59 Gene

No data available for Paralogs for DFNA59 Gene

Variants for DFNA59 Gene

Additional Variant Information for DFNA59 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 DFNA59 Gene

Disorders for DFNA59 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DFNA59 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal dominant 59
  • dfna59
autosomal dominant nonsyndromic deafness
  • autosomal dominant deafness
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNA59: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNA59 Gene

Publications for DFNA59 Gene

  1. A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3. (PMID: 19030898) Chatterjee A … Anand A (Human genetics 2009) 2 3 58

Products for DFNA59 Gene

Sources for DFNA59 Gene

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