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Aliases for DFNA31 Gene

Aliases for DFNA31 Gene

  • Deafness, Autosomal Dominant 31 2 3

External Ids for DFNA31 Gene

Previous GeneCards Identifiers for DFNA31 Gene

  • GC00U910147

Summaries for DFNA31 Gene

GeneCards Summary for DFNA31 Gene

DFNA31 (Deafness, Autosomal Dominant 31) is a Genetic Locus. Diseases associated with DFNA31 include Deafness, Autosomal Dominant 31 and Autosomal Dominant Nonsyndromic Deafness.

Additional gene information for DFNA31 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 DFNA31 Gene

Genomics for DFNA31 Gene

Genomic Locations for DFNA31 Gene

Genomic Locations for DFNA31 Gene
Unknown strand

Genomic View for DFNA31 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for DFNA31 Gene

Proteins for DFNA31 Gene

Post-translational modifications for DFNA31 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNA31 Gene

Domains & Families for DFNA31 Gene

Gene Families for DFNA31 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNA31: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNA31 Gene

Function for DFNA31 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 DFNA31 Gene

Localization for DFNA31 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 DFNA31 Gene

Pathways & Interactions for DFNA31 Gene

SuperPathways for DFNA31 Gene

No Data Available

Interacting Proteins for DFNA31 Gene

Gene Ontology (GO) - Biological Process for DFNA31 Gene


No data available for Pathways by source and SIGNOR curated interactions for DFNA31 Gene

Drugs & Compounds for DFNA31 Gene

No Compound Related Data Available

Transcripts for DFNA31 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for DFNA31 Gene

No ASD Table

Relevant External Links for DFNA31 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for DFNA31 Gene

Expression for DFNA31 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNA31 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 DFNA31 Gene

Orthologs for DFNA31 Gene

No data available for Orthologs and Evolution for DFNA31 Gene

Paralogs for DFNA31 Gene

No data available for Paralogs for DFNA31 Gene

Variants for DFNA31 Gene

Additional Variant Information for DFNA31 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 DFNA31 Gene

Disorders for DFNA31 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DFNA31 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal dominant 31
  • dfna31
autosomal dominant nonsyndromic deafness
  • autosomal dominant deafness
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNA31: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNA31 Gene

Publications for DFNA31 Gene

  1. A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3. (PMID: 14729819) Snoeckx RL … Van Camp G (Journal of medical genetics 2004) 2 3 58

Products for DFNA31 Gene

Sources for DFNA31 Gene

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