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Aliases for DFNA30 Gene

Aliases for DFNA30 Gene

  • Deafness, Autosomal Dominant 30 2 3

External Ids for DFNA30 Gene

Summaries for DFNA30 Gene

GeneCards Summary for DFNA30 Gene

DFNA30 (Deafness, Autosomal Dominant 30) is a Genetic Locus. Diseases associated with DFNA30 include Deafness, Autosomal Dominant 30 and Autosomal Dominant Nonsyndromic Deafness.

Additional gene information for DFNA30 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 DFNA30 Gene

Genomics for DFNA30 Gene

Genomic Locations for DFNA30 Gene

Genomic Locations for DFNA30 Gene
Unknown strand

Genomic View for DFNA30 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for DFNA30 Gene

Proteins for DFNA30 Gene

Post-translational modifications for DFNA30 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNA30 Gene

Domains & Families for DFNA30 Gene

Gene Families for DFNA30 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNA30: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNA30 Gene

Function for DFNA30 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 DFNA30 Gene

Localization for DFNA30 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 DFNA30 Gene

Pathways & Interactions for DFNA30 Gene

SuperPathways for DFNA30 Gene

No Data Available

Interacting Proteins for DFNA30 Gene

Gene Ontology (GO) - Biological Process for DFNA30 Gene


No data available for Pathways by source and SIGNOR curated interactions for DFNA30 Gene

Drugs & Compounds for DFNA30 Gene

No Compound Related Data Available

Transcripts for DFNA30 Gene

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for DFNA30 Gene

No ASD Table

Relevant External Links for DFNA30 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for DFNA30 Gene

Expression for DFNA30 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNA30 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 DFNA30 Gene

Orthologs for DFNA30 Gene

No data available for Orthologs and Evolution for DFNA30 Gene

Paralogs for DFNA30 Gene

No data available for Paralogs for DFNA30 Gene

Variants for DFNA30 Gene

Additional Variant Information for DFNA30 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 DFNA30 Gene

Disorders for DFNA30 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DFNA30 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal dominant 30
  • dfna30
autosomal dominant nonsyndromic deafness
  • autosomal dominant deafness
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNA30: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNA30 Gene

Publications for DFNA30 Gene

  1. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26. (PMID: 11571554) Mangino M … Dallapiccola B (European journal of human genetics : EJHG 2001) 2 3 58

Products for DFNA30 Gene

Sources for DFNA30 Gene

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