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Aliases for DFNA58 Gene

Aliases for DFNA58 Gene

  • Deafness, Autosomal Dominant 58 2 3

External Ids for DFNA58 Gene

Previous GeneCards Identifiers for DFNA58 Gene

  • GC00U922574

Summaries for DFNA58 Gene

Entrez Gene Summary for DFNA58 Gene

  • This locus was identified to map between markers D2S2259 and D2S2114 in a Brazilian family with 12 individuals affected by bilateral post-lingual and progressive hearing loss. [provided by RefSeq, Feb 2010]

GeneCards Summary for DFNA58 Gene

DFNA58 (Deafness, Autosomal Dominant 58) is a Genetic Locus. Diseases associated with DFNA58 include Deafness, Autosomal Dominant 58 and Autosomal Dominant Nonsyndromic Deafness.

Additional gene information for DFNA58 Gene

No data available for CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for DFNA58 Gene

Genomics for DFNA58 Gene

Genomic Locations for DFNA58 Gene

Genomic Locations for DFNA58 Gene
Unknown strand

Genomic View for DFNA58 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for DFNA58 Gene

Proteins for DFNA58 Gene

Post-translational modifications for DFNA58 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNA58 Gene

Domains & Families for DFNA58 Gene

Gene Families for DFNA58 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNA58: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNA58 Gene

Function for DFNA58 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 DFNA58 Gene

Localization for DFNA58 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 DFNA58 Gene

Pathways & Interactions for DFNA58 Gene

SuperPathways for DFNA58 Gene

No Data Available

Interacting Proteins for DFNA58 Gene

Gene Ontology (GO) - Biological Process for DFNA58 Gene


No data available for Pathways by source and SIGNOR curated interactions for DFNA58 Gene

Drugs & Compounds for DFNA58 Gene

No Compound Related Data Available

Transcripts for DFNA58 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for DFNA58 Gene

No ASD Table

Relevant External Links for DFNA58 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for DFNA58 Gene

Expression for DFNA58 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNA58 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 DFNA58 Gene

Orthologs for DFNA58 Gene

No data available for Orthologs and Evolution for DFNA58 Gene

Paralogs for DFNA58 Gene

No data available for Paralogs for DFNA58 Gene

Variants for DFNA58 Gene

Additional Variant Information for DFNA58 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 DFNA58 Gene

Disorders for DFNA58 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DFNA58 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal dominant 58
  • dfna58
autosomal dominant nonsyndromic deafness
  • autosomal dominant deafness
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNA58: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNA58 Gene

Publications for DFNA58 Gene

  1. A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21. (PMID: 19159392) Lezirovitz K … Mingroni-Netto RC (Clinical genetics 2009) 2 3 58

Products for DFNA58 Gene

Sources for DFNA58 Gene

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