Free for academic non-profit institutions. Other users need a Commercial license

Aliases for DFNA21 Gene

Aliases for DFNA21 Gene

  • Deafness, Autosomal Dominant 21 2 3

External Ids for DFNA21 Gene

Summaries for DFNA21 Gene

GeneCards Summary for DFNA21 Gene

DFNA21 (Deafness, Autosomal Dominant 21) is a Genetic Locus. Diseases associated with DFNA21 include Deafness, Autosomal Dominant 21 and Autosomal Dominant Nonsyndromic Deafness.

Additional gene information for DFNA21 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 DFNA21 Gene

Genomics for DFNA21 Gene

Genomic Locations for DFNA21 Gene

Genomic Locations for DFNA21 Gene
Unknown strand

Genomic View for DFNA21 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for DFNA21 Gene

Proteins for DFNA21 Gene

Post-translational modifications for DFNA21 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNA21 Gene

Domains & Families for DFNA21 Gene

Gene Families for DFNA21 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNA21: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNA21 Gene

Function for DFNA21 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 DFNA21 Gene

Localization for DFNA21 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 DFNA21 Gene

Pathways & Interactions for DFNA21 Gene

SuperPathways for DFNA21 Gene

No Data Available

Interacting Proteins for DFNA21 Gene

Gene Ontology (GO) - Biological Process for DFNA21 Gene


No data available for Pathways by source and SIGNOR curated interactions for DFNA21 Gene

Drugs & Compounds for DFNA21 Gene

No Compound Related Data Available

Transcripts for DFNA21 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for DFNA21 Gene

No ASD Table

Relevant External Links for DFNA21 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for DFNA21 Gene

Expression for DFNA21 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNA21 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 DFNA21 Gene

Orthologs for DFNA21 Gene

No data available for Orthologs and Evolution for DFNA21 Gene

Paralogs for DFNA21 Gene

No data available for Paralogs for DFNA21 Gene

Variants for DFNA21 Gene

Additional Variant Information for DFNA21 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 DFNA21 Gene

Disorders for DFNA21 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DFNA21 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal dominant 21
  • dfna21
autosomal dominant nonsyndromic deafness
  • autosomal dominant deafness
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNA21: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNA21 Gene

Publications for DFNA21 Gene

  1. Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3. (PMID: 16007628) de Brouwer AP … Kremer H (American journal of medical genetics. Part A 2005) 2 3 58
  2. Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21). (PMID: 10764236) Kunst H … Cremers C (Clinical otolaryngology and allied sciences 2000) 2 3 58
  3. Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes. (PMID: 10890148) Bom SJ … Cremers CW (British journal of audiology 1999) 2 3 58

Products for DFNA21 Gene

Sources for DFNA21 Gene

Loading form....