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Aliases for DFNB51 Gene

Aliases for DFNB51 Gene

  • Deafness, Autosomal Recessive 51 2 3

External Ids for DFNB51 Gene

Previous GeneCards Identifiers for DFNB51 Gene

  • GC00U920416

Summaries for DFNB51 Gene

GeneCards Summary for DFNB51 Gene

DFNB51 (Deafness, Autosomal Recessive 51) is a Genetic Locus. Diseases associated with DFNB51 include Deafness, Autosomal Recessive 51 and Nonsyndromic Deafness.

Additional gene information for DFNB51 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 DFNB51 Gene

Genomics for DFNB51 Gene

Genomic Location for DFNB51 Gene

Chromosome:
11
Orientation:
Unknown strand

Genomic View for DFNB51 Gene


Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for DFNB51 Gene

Proteins for DFNB51 Gene

Post-translational modifications for DFNB51 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNB51 Gene

Domains & Families for DFNB51 Gene

Gene Families for DFNB51 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNB51: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNB51 Gene

Function for DFNB51 Gene

Animal Model Products

CRISPR Products

Clone Products

  • Applied Biological Materials Clones for DFNB51
  • 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 DFNB51 Gene

Localization for DFNB51 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 DFNB51 Gene

Pathways & Interactions for DFNB51 Gene

SuperPathways for DFNB51 Gene

No Data Available

Interacting Proteins for DFNB51 Gene

Gene Ontology (GO) - Biological Process for DFNB51 Gene

None

No data available for Pathways by source and SIGNOR curated interactions for DFNB51 Gene

Drugs & Compounds for DFNB51 Gene

No Compound Related Data Available

Transcripts for DFNB51 Gene

CRISPR Products

Clone Products

  • Applied Biological Materials Clones for DFNB51
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

Alternative Splicing Database (ASD) splice patterns (SP) for DFNB51 Gene

No ASD Table

Relevant External Links for DFNB51 Gene

ECgene alternative splicing isoforms for
DFNB51

No data available for mRNA/cDNA for DFNB51 Gene

Expression for DFNB51 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNB51 Gene:

DFNB51
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 DFNB51 Gene

Orthologs for DFNB51 Gene

No data available for Orthologs and Evolution for DFNB51 Gene

Paralogs for DFNB51 Gene

No data available for Paralogs for DFNB51 Gene

Variants for DFNB51 Gene

Relevant External Links for DFNB51 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for
DFNB51

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 DFNB51 Gene

Disorders for DFNB51 Gene

MalaCards: The human disease database

(2) MalaCards diseases for DFNB51 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal recessive 51
  • autosomal recessive nonsyndromic deafness 51
nonsyndromic deafness
  • nonsyndromic hearing loss
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNB51: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNB51 Gene

Publications for DFNB51 Gene

  1. A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12. (PMID: 16158433) Shaikh RS … Riazuddin S (American journal of medical genetics. Part A 2005) 2 3 60

Products for DFNB51 Gene

Sources for DFNB51 Gene

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