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Aliases for DFNB81 Gene

Aliases for DFNB81 Gene

  • Deafness, Autosomal Recessive 81 2 3

External Ids for DFNB81 Gene

Previous GeneCards Identifiers for DFNB81 Gene

  • GC00U922961

Summaries for DFNB81 Gene

GeneCards Summary for DFNB81 Gene

DFNB81 (Deafness, Autosomal Recessive 81) is a Genetic Locus. Diseases associated with DFNB81 include Perrault Syndrome 3.

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 DFNB81 Gene

Genomics for DFNB81 Gene

Genomic Location for DFNB81 Gene

Unknown strand

Genomic View for DFNB81 Gene

Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for DFNB81 Gene

Proteins for DFNB81 Gene

Post-translational modifications for DFNB81 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNB81 Gene

Domains & Families for DFNB81 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 DFNB81 Gene

Function for DFNB81 Gene

No data available for Molecular function , Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for DFNB81 Gene

Localization for DFNB81 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for DFNB81 Gene

Pathways & Interactions for DFNB81 Gene

SuperPathways for DFNB81 Gene

No Data Available

Interacting Proteins for DFNB81 Gene

Gene Ontology (GO) - Biological Process for DFNB81 Gene


No data available for Pathways by source and SIGNOR curated interactions for DFNB81 Gene

Drugs & Compounds for DFNB81 Gene

No Compound Related Data Available

Expression for DFNB81 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 , mRNA Expression by UniProt/SwissProt and Protein tissue co-expression partners for DFNB81 Gene

Orthologs for DFNB81 Gene

No data available for Orthologs and Evolution for DFNB81 Gene

Paralogs for DFNB81 Gene

No data available for Paralogs for DFNB81 Gene

Variants for DFNB81 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) , Variation tolerance and Relevant External Links for DFNB81 Gene

Disorders for DFNB81 Gene

MalaCards: The human disease database

(1) MalaCards diseases for DFNB81 Gene - From: OMIM

Disorder Aliases PubMed IDs
perrault syndrome 3
  • prlts3
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNB81: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNB81 Gene

Publications for DFNB81 Gene

  1. Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p. (PMID: 21660509) Rehman A.U. … Friedman T.B. (Hum. Genet. 2011) 2 3 67

Products for DFNB81 Gene

Sources for DFNB81 Gene