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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.

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 DFNA42 Gene

Genomics for DFNA42 Gene

Genomic Location for DFNA42 Gene

Chromosome:
5
Orientation:
Unknown strand

Genomic View for DFNA42 Gene


Cytogenetic band:
GeneLoc Logo Gene Density

No data available for 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

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 DFNA42 Gene

Function for DFNA42 Gene

No data available for Molecular function , Enzyme Numbers (IUBMB) , 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 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

None

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

Drugs & Compounds for DFNA42 Gene

No Compound Related Data Available

Expression for DFNA42 Gene

No Expression Related Data Available

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 Protein tissue co-expression partners 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

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Sequence variations from dbSNP and Humsavar , Structural Variations from Database of Genomic Variants (DGV) , Variation tolerance and Relevant External Links for DFNA42 Gene

Disorders for DFNA42 Gene

MalaCards: The human disease database

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

Disorder Aliases PubMed IDs
deafness, autosomal dominant 52
- 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. (J. Hum. Genet. 2002) 2 3 67

Products for DFNA42 Gene

Sources for DFNA42 Gene

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