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Aliases for DFNA42 Gene

Aliases for DFNA42 Gene

  • Deafness, Autosomal Dominant 42 2 3
  • Deafness, Autosomal Dominant 52 2 3
  • DFNA52 3

External Ids for DFNA42 Gene

Previous HGNC Symbols for DFNA42 Gene

  • DFNA52

Previous GeneCards Identifiers for DFNA42 Gene

  • GC04U990145

Summaries for DFNA42 Gene

GeneCards Summary for DFNA42 Gene

DFNA42 (Deafness, Autosomal Dominant 42) is a Genetic Locus. Diseases associated with DFNA42 include Deafness, Autosomal Dominant 52 and Autosomal Dominant Nonsyndromic Deafness.

Additional gene information for DFNA42 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 DFNA42 Gene

Genomics for DFNA42 Gene

Genomic Locations for DFNA42 Gene

Genomic Locations for DFNA42 Gene
Unknown strand

Genomic View for DFNA42 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for DFNA42 Gene

Proteins for DFNA42 Gene

Post-translational modifications for DFNA42 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNA42 Gene

Domains & Families for DFNA42 Gene

Gene Families for DFNA42 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNA42: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNA42 Gene

Function for DFNA42 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 DFNA42 Gene

Localization for DFNA42 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 DFNA42 Gene

Pathways & Interactions for DFNA42 Gene

SuperPathways for DFNA42 Gene

No Data Available

Interacting Proteins for DFNA42 Gene

Gene Ontology (GO) - Biological Process for DFNA42 Gene


No data available for Pathways by source and SIGNOR curated interactions for DFNA42 Gene

Drugs & Compounds for DFNA42 Gene

No Compound Related Data Available

Transcripts for DFNA42 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for DFNA42 Gene

No ASD Table

Relevant External Links for DFNA42 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for DFNA42 Gene

Expression for DFNA42 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNA42 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 DFNA42 Gene

Orthologs for DFNA42 Gene

No data available for Orthologs and Evolution for DFNA42 Gene

Paralogs for DFNA42 Gene

No data available for Paralogs for DFNA42 Gene

Variants for DFNA42 Gene

Additional Variant Information for DFNA42 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 DFNA42 Gene

Disorders for DFNA42 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DFNA42 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal dominant 52
  • dfna52
autosomal dominant nonsyndromic deafness
  • autosomal dominant deafness
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNA42: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNA42 Gene

Publications for DFNA42 Gene

  1. A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree. (PMID: 12522684) Xia J … Xia K (Journal of human genetics 2002) 2 3 58

Products for DFNA42 Gene

Sources for DFNA42 Gene

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