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Aliases for DFNA47 Gene

Aliases for DFNA47 Gene

  • Deafness, Autosomal Dominant 47 2 3
  • DFNB83 3

External Ids for DFNA47 Gene

Previous GeneCards Identifiers for DFNA47 Gene

  • GC00U991230

Summaries for DFNA47 Gene

GeneCards Summary for DFNA47 Gene

DFNA47 (Deafness, Autosomal Dominant 47) is a Genetic Locus. Diseases associated with DFNA47 include Deafness, Autosomal Dominant 47.

Additional gene information for DFNA47 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 DFNA47 Gene

Genomics for DFNA47 Gene

Genomic Location for DFNA47 Gene

Chromosome:
9
Orientation:
Unknown strand

Genomic View for DFNA47 Gene


Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for DFNA47 Gene

Proteins for DFNA47 Gene

Post-translational modifications for DFNA47 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNA47 Gene

Domains & Families for DFNA47 Gene

Gene Families for DFNA47 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNA47: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNA47 Gene

Function for DFNA47 Gene

Animal Model Products

CRISPR Products

Clone Products

  • Applied Biological Materials Clones for DFNA47
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

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 DFNA47 Gene

Localization for DFNA47 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 DFNA47 Gene

Pathways & Interactions for DFNA47 Gene

SuperPathways for DFNA47 Gene

No Data Available

Interacting Proteins for DFNA47 Gene

Gene Ontology (GO) - Biological Process for DFNA47 Gene

None

No data available for Pathways by source and SIGNOR curated interactions for DFNA47 Gene

Drugs & Compounds for DFNA47 Gene

No Compound Related Data Available

Transcripts for DFNA47 Gene

CRISPR Products

Clone Products

  • Applied Biological Materials Clones for DFNA47
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

Alternative Splicing Database (ASD) splice patterns (SP) for DFNA47 Gene

No ASD Table

Relevant External Links for DFNA47 Gene

ECgene alternative splicing isoforms for
DFNA47

No data available for mRNA/cDNA for DFNA47 Gene

Expression for DFNA47 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNA47 Gene:

DFNA47
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 DFNA47 Gene

Orthologs for DFNA47 Gene

No data available for Orthologs and Evolution for DFNA47 Gene

Paralogs for DFNA47 Gene

No data available for Paralogs for DFNA47 Gene

Variants for DFNA47 Gene

Relevant External Links for DFNA47 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for
DFNA47

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 DFNA47 Gene

Disorders for DFNA47 Gene

MalaCards: The human disease database

(1) MalaCards diseases for DFNA47 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal dominant 47
  • autosomal dominant nonsyndromic deafness 47
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNA47: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNA47 Gene

Publications for DFNA47 Gene

  1. A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family. (PMID: 12634859) D'Adamo P … Gasparini P (European journal of human genetics : EJHG 2003) 2 3 60

Products for DFNA47 Gene

Sources for DFNA47 Gene

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