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Aliases for DFNB65 Gene

Aliases for DFNB65 Gene

  • Deafness, Autosomal Recessive 65 2 3

External Ids for DFNB65 Gene

Summaries for DFNB65 Gene

GeneCards Summary for DFNB65 Gene

DFNB65 (Deafness, Autosomal Recessive 65) is a Genetic Locus. Diseases associated with DFNB65 include Deafness, Autosomal Recessive 65 and Deafness, Autosomal Recessive.

Additional gene information for DFNB65 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 DFNB65 Gene

Genomics for DFNB65 Gene

Genomic Locations for DFNB65 Gene

Genomic Locations for DFNB65 Gene
Unknown strand

Genomic View for DFNB65 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for GeneHancer (GH) Regulatory Elements and RefSeq DNA sequence for DFNB65 Gene

Proteins for DFNB65 Gene

Post-translational modifications for DFNB65 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNB65 Gene

Domains & Families for DFNB65 Gene

Gene Families for DFNB65 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNB65: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNB65 Gene

Function for DFNB65 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 DFNB65 Gene

Localization for DFNB65 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 DFNB65 Gene

Pathways & Interactions for DFNB65 Gene

SuperPathways for DFNB65 Gene

No Data Available

Interacting Proteins for DFNB65 Gene

Gene Ontology (GO) - Biological Process for DFNB65 Gene


No data available for Pathways by source and SIGNOR curated interactions for DFNB65 Gene

Drugs & Compounds for DFNB65 Gene

No Compound Related Data Available

Transcripts for DFNB65 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for DFNB65 Gene

No ASD Table

Relevant External Links for DFNB65 Gene

ECgene alternative splicing isoforms for

No data available for mRNA/cDNA for DFNB65 Gene

Expression for DFNB65 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNB65 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 DFNB65 Gene

Orthologs for DFNB65 Gene

No data available for Orthologs and Evolution for DFNB65 Gene

Paralogs for DFNB65 Gene

No data available for Paralogs for DFNB65 Gene

Variants for DFNB65 Gene

Additional Variant Information for DFNB65 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 DFNB65 Gene

Disorders for DFNB65 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DFNB65 Gene - From: OMIM and GeneCards

- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNB65: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNB65 Gene

Publications for DFNB65 Gene

  1. Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2-q13.32. (PMID: 16596430) Tariq A … Leal SM (Journal of molecular medicine (Berlin, Germany) 2006) 2 3 58

Products for DFNB65 Gene

Sources for DFNB65 Gene

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