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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.

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 DFNA21 Gene

Genomics for DFNA21 Gene

Genomic Location for DFNA21 Gene

Unknown strand

Genomic View for DFNA21 Gene

Cytogenetic band:

No data available for 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 for DFNA21 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 DFNA21 Gene

Function for DFNA21 Gene

No data available for Molecular function , Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Phenotypes , Animal Models , miRNA , Transcription Factor Targeting and HOMER Transcription for DFNA21 Gene

Localization for DFNA21 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for DFNA21 Gene

Pathways 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 for DFNA21 Gene

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

No Expression Related Data Available

Primer Products

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 Expression partners 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

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 Relevant External Links for DFNA21 Gene

Disorders for DFNA21 Gene

MalaCards: The human disease database

MalaCards: The human disease database.

Search for DFNA21 Gene in MalaCards »

(1) Disease for DFNA21 Gene

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

No data available for OMIM , UniProtKB/Swiss-Prot , University of Copenhagen DISEASES , Novoseek inferred disease relationships , Genatlas and External Links for DFNA21 Gene

Publications for DFNA21 Gene

  1. 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. (Clin Otolaryngol Allied Sci 2000) 2 3
  2. Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes. (PMID: 10890148) Bom S.J. … Cremers C.W. (Br J Audiol 1999) 2 3
  3. Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3. (PMID: 16007628) de Brouwer A.P. … Kremer H. (Am. J. Med. Genet. A 2005) 2 3

Products for DFNA21 Gene

Sources for DFNA21 Gene

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