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Aliases for DFNB96 Gene

Aliases for DFNB96 Gene

  • Deafness, Autosomal Recessive 96 2 3

External Ids for DFNB96 Gene

Previous GeneCards Identifiers for DFNB96 Gene

  • GC00U931357

Summaries for DFNB96 Gene

GeneCards Summary for DFNB96 Gene

DFNB96 (Deafness, Autosomal Recessive 96) is a Genetic Locus. Diseases associated with DFNB96 include Deafness, Autosomal Recessive 96.

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 DFNB96 Gene

Genomics for DFNB96 Gene

Genomic Location for DFNB96 Gene

Chromosome:
1
Orientation:
Unknown strand

Genomic View for DFNB96 Gene


Cytogenetic band:
GeneLoc Logo Gene Density

No data available for Regulatory Elements and RefSeq DNA sequence for DFNB96 Gene

Proteins for DFNB96 Gene

Post-translational modifications for DFNB96 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DFNB96 Gene

Domains & Families for DFNB96 Gene

Gene Families for DFNB96 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with DFNB96: view

No data available for Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DFNB96 Gene

Function for DFNB96 Gene

Animal Model Products

Clone Products

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 DFNB96 Gene

Localization for DFNB96 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for DFNB96 Gene

Pathways & Interactions for DFNB96 Gene

SuperPathways for DFNB96 Gene

No Data Available

Interacting Proteins for DFNB96 Gene

Gene Ontology (GO) - Biological Process for DFNB96 Gene

None

No data available for Pathways by source and SIGNOR curated interactions for DFNB96 Gene

Drugs & Compounds for DFNB96 Gene

No Compound Related Data Available

Transcripts for DFNB96 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for DFNB96 Gene

No ASD Table

Relevant External Links for DFNB96 Gene

ECgene alternative splicing isoforms for
DFNB96

No data available for mRNA/cDNA for DFNB96 Gene

Expression for DFNB96 Gene

NURSA nuclear receptor signaling pathways regulating expression of DFNB96 Gene:

DFNB96
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 DFNB96 Gene

Orthologs for DFNB96 Gene

No data available for Orthologs and Evolution for DFNB96 Gene

Paralogs for DFNB96 Gene

No data available for Paralogs for DFNB96 Gene

Variants for DFNB96 Gene

Relevant External Links for DFNB96 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for
DFNB96

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 DFNB96 Gene

Disorders for DFNB96 Gene

MalaCards: The human disease database

(1) MalaCards diseases for DFNB96 Gene - From: OMIM and GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal recessive 96
  • autosomal recessive nonsyndromic deafness 96
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with DFNB96: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for DFNB96 Gene

Publications for DFNB96 Gene

  1. A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13. (PMID: 21937999) Ansar M. … Leal S.M. (J. Hum. Genet. 2011) 2 3 64

Products for DFNB96 Gene

Sources for DFNB96 Gene

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